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Item 1A. Risk Factors

2022-03-30 compared with 2021-03-16 · 1255 added, 1318 removed, 275 unchanged (90% of the section changed)

An investment in our common stock involves

a high degree of risk.

You should carefully consider the following risk factors and the other information in this Annual Report

on Form 10-K before investing in our common stock.

Our business and results of operations could be seriously harmed by any of the

following risks.

investment in our common stock involves a high degree of risk.

You should carefully consider the following risk factors and the other

information in this Annual Report on Form 10-K before investing in our common stock.

Our business and results of operations could be

seriously harmed by any of the following risks.

The risks set out below are not the only risks we face.

Additional risks and uncertainties not currently known

to us or that we currently deem to be immaterial also may materially adversely affect our business, financial condition and/or

operating results.

If any of the following events occur, our business, financial condition and results of operations could be materially

adversely affected.

In such case, the value and trading price of our common stock could decline, and you may lose all or part of

your investment.

Risks Related to Our Financial Position

and Need for Capital

We have generated no revenue from commercial

sales to date and our future profitability is uncertain.

We were incorporated in May 2017 and have a

limited operating history and our business is subject to all of the risks inherent in the establishment of a new business enterprise.

Our likelihood of success must be considered in light of the problems, expenses, difficulties, complications and delays frequently

encountered in connection with development and expansion of a new business enterprise.

Since inception, we have incurred losses

and expect to continue to operate at a net loss for at least the next several years as we commence our research and development

Additional risks and uncertainties

not currently known to us or that we currently deem to be immaterial also may materially adversely affect our business, financial condition

and/or operating results.

If any of the following events occur, our business, financial condition and results of operations could be

materially adversely affected.

In such case, the value and trading price of our common stock could decline, and you may lose all or part

of your investment.

Related to Our Financial Position and Need for Capital

have generated no revenue from commercial sales to date and our future profitability is uncertain.

were incorporated in May 2017 and have a limited operating history and our business is subject to all of the risks inherent in the establishment

of a new business enterprise.

Our likelihood of success must be considered in light of the problems, expenses, difficulties, complications

and delays frequently encountered in connection with development and expansion of a new business enterprise.

Since inception, we have

incurred losses and expect to continue to operate at a net loss for at least the next several years as we commence our research and development

efforts, conduct clinical trials and develop manufacturing, sales, marketing and distribution capabilities.

Our net losses for

the years ended December 31, 2020 and 2019 were $7,197,816 and $7,704,636, respectively, and our accumulated deficit as of December

31, 2020 and 2019 was $19,413,458 and $12,215,642, respectively.

There can be no assurance that the products under development

by us will be approved for sale in the U.S.

Our net losses for the years

ended December 31, 2021 and 2020 were $14,313,705 and $7,197,816, respectively, and our accumulated deficit as of December 31, 2021 and

2020 was $33,727,163 and $19,413,458, respectively.

There can be no assurance that the products under development by us will be approved

for sale in the U.S.

or elsewhere.

Furthermore, there can be no assurance that if such products are approved

they will be successfully commercialized, and the extent of our future losses and the timing of our profitability are highly uncertain.

If we are unable to achieve profitability, we may be unable to continue our operations.

If we fail to obtain the capital necessary

to fund our operations, we will be unable to continue or complete our product development and you will likely lose your entire

We will need to continue to seek capital from

time to time to continue development of our product candidates.

We cannot provide any assurances that any revenues that we may

generate in the future will be sufficient to fund our ongoing operations.

We believe that we will need to raise substantial additional

capital to fund our operations and the development and commercialization of our product candidates.

Our business or operations may change in a

manner that may consume available funds more rapidly than anticipated and substantial additional funding may be required to maintain

operations, fund expansion, commercialize our product candidates, develop new or enhanced products, acquire complementary products,

business or technologies or otherwise respond to competitive pressures and opportunities, such as a change in the regulatory environment

or a change in preferred treatment modalities.

In addition, we may need to accelerate the growth of our sales capabilities and

distribution beyond what is currently envisioned, and this would require additional capital.

However, we may not be able to secure

funding on favorable terms, if at all.

If we cannot raise adequate funds to satisfy

our capital requirements, we may have to delay, scale back or eliminate our research and development activities, clinical studies

or operations.

We may also be required to obtain funds through arrangements with collaborators, which arrangements may require

us to relinquish rights to certain intellectual property, technologies or products that we otherwise would not consider relinquishing,

Furthermore, there can be no assurance that if such products are approved they will be successfully

commercialized, and the extent of our future losses and the timing of our profitability are highly uncertain.

If we are unable to achieve

profitability, we may be unable to continue our operations.

we fail to obtain the capital necessary to fund our operations, we will be unable to continue or complete our product development and

you will likely lose your entire investment.

will need to continue to seek capital from time to time to continue development of our product candidates.

We cannot provide any assurances

that any revenues that we may generate in the future will be sufficient to fund our ongoing operations.

We believe that we will need

to raise substantial additional capital to fund our operations and the development and commercialization of our product candidates.

business or operations may change in a manner that may consume available funds more rapidly than anticipated and substantial additional

funding may be required to maintain operations, fund expansion, commercialize our product candidates, develop new or enhanced products,

acquire complementary products, business or technologies or otherwise respond to competitive pressures and opportunities, such as a change

in the regulatory environment or a change in preferred treatment modalities.

In addition, we may need to accelerate the growth of our

sales capabilities and distribution beyond what is currently envisioned, and this would require additional capital.

However, we may not

be able to secure funding on favorable terms, if at all.

we cannot raise adequate funds to satisfy our capital requirements, we may have to delay, scale back or eliminate our research and development

activities, clinical studies or operations.

We may also be required to obtain funds through arrangements with collaborators, which arrangements

may require us to relinquish rights to certain intellectual property, technologies or products that we otherwise would not consider relinquishing,

including rights to future product candidates or certain major geographic markets.

This could result in sharing revenues which

we might otherwise retain for ourselves.

This could result in sharing revenues which we might

otherwise retain for ourselves.

Any of these actions may harm our business, financial condition and results of operations.

The amount of capital we may need depends on

many factors, including the progress, timing and scope of our product development programs;

the progress, timing and scope of our

pre-clinical studies and clinical trials;

amount of capital we may need depends on many factors, including the progress, timing and scope of our product development programs;

the progress, timing and scope of our pre-clinical studies and clinical trials;

the time and cost necessary to obtain regulatory approvals;

the time and cost necessary

to further develop manufacturing processes and arrange for contract manufacturing;

our ability to enter into and maintain collaborative,

licensing and other commercial relationships;

and our partners’

commitment of time and resources to the development and commercialization

of our products.

Even if we can raise additional funding,

we may be required to do so on terms that are dilutive to you.

The capital markets have been unpredictable

in the recent past for unprofitable companies such as ours.

The amount of capital that a company such as ours is able to raise

often depends on variables that are beyond our control.

As a result, we may not be able to secure financing on terms attractive

to us, or at all.

If we are able to consummate a financing arrangement, the amount raised may not be sufficient to meet our future

If adequate funds are not available on acceptable terms, or at all, our business, including our results of operations, financial

condition and our continued viability will be materially adversely affected.

Risks Related to Product Development, Regulatory

Approval, Manufacturing and Commercialization

We are dependent upon the clinical success

of our licensed products and technologies.

If we are unable to generate revenues from our licensed products and technologies, our

ability to create shareholder value may be limited.

We do not currently generate revenues from

any of our product candidates, and we may not be successful in obtaining regulatory approvals to commence our clinical trials.

If we do not obtain such approvals, the time in which we expect to commence clinical programs for our product candidates will be

extended and such extension may increase our expenses and our need for additional capital.

Moreover, there is no guarantee that

our clinical trials will be successful or that we will continue clinical development in support of an approval from the regulatory

agencies for any indication.

We note that most drug candidates never reach the clinical stage and even those that do commence clinical

development have only a small chance of successfully completing clinical development and gaining regulatory approval.

our business currently depends entirely on the successful development, regulatory approval and commercialization of our product

candidates, which may never occur.

Although we have entered into the Voltron

Agreement pursuant to which we and HaloVax intend to jointly develop products to prevent COVID-19, no assurance can be given as

to when, if ever, we will be able to develop any products for such purpose and if developed that such products will be successfully

commercialized.

On March 23, 2020, we entered into the Voltron

Agreement pursuant to which we and HaloVax will work to jointly develop potential products candidates to prevent COVID-19;

no assurance can be given as to when, if ever, we will be able to develop any products for such purpose.

Furthermore, we are subject

to risks including, but not limited to, the following with respect to the development of a treatment for COVID-19:

the Emergency Use Authorization marketing approval processes of the FDA are lengthy, time consuming and inherently unpredictable, and we cannot guarantee that we will ever have a marketable product;

we may encounter substantial delays in completing our clinical studies which in turn will require additional costs, or we may fail to demonstrate adequate safety and efficacy to the satisfaction of applicable regulatory authorities;

conducting successful clinical studies may require the enrollment of large numbers of patients, and suitable patients may be difficult to identify and recruit;

to be commercially successful, physicians must be persuaded that using our products are effective alternatives to other existing therapies and treatments;

we may depend on third parties for manufacturing our proposed product candidates and any conflicts with such partners could delay or prevent the development or commercialization of such product candidates;

if third-party contract manufacturers upon whom we rely to formulate and manufacture our product candidates do not perform, fail to manufacture according to our specifications or fail to comply with strict regulations, our clinical studies could be adversely affected and the development of our product candidates could be delayed or terminated or we could incur significant additional expenses;

adverse events involving our products may lead the FDA to delay or deny clearance for our products or result in product recalls that could harm our reputation, business and financial results;

if we fail to comply with healthcare regulations, we could face substantial enforcement actions, including civil and criminal penalties and our business, operations and financial condition could be adversely affected.

If our joint venture with HaloVax is

not successful or if we fail to realize the benefits we anticipate from such joint venture, we may not be able to capitalize on

the full market potential of our potential products.

On March 23, 2020, we entered into the Voltron

Agreement to form a joint venture entity named HaloVax to jointly develop potential product candidates for the prevention of the

COVID-19 based upon certain technology that had been exclusively licensed by Voltron from Mass Gen.

Pursuant to the terms of the

Voltron Agreement we are entitled to receive sales-based royalties at low single digit percentages.

In addition, on March 23, 2020

and May 28, 2020, we entered into membership purchase agreements with HaloVax pursuant to which we purchased 5% and 1% of HaloVax’s

outstanding membership interests, respectively.

Furthermore, we shall contribute proceeds of the development of products to prevent

If and to the extent we and HaloVax are unable to develop potential product candidates for the prevention of COVID-19,

we will not be entitled to any sale-based royalties the value of our ownership interest in HaloVax could decline in which case

we may lose all or part of our investment in HaloVax.

While Voltron has

agreed to cooperate and use commercially reasonable efforts to exchange information and resources that will lead to the development

activities, and established a Joint Development Committee consisting of seven members, two of which were selected by us, to plan,

review, coordinate and oversee the performance of the development activities and timelines with respect to development activities,

we have limited contractual rights to direct its activities.

Moreover, we will not have any other control with respect to the operations

Therefore, HaloVax will have a greater influence with respect to its commercialization efforts and other operations.

In general, our joint venture with HaloVax subjects us to a number of related risks including that:

the time and cost necessary to further develop manufacturing processes and arrange for contract manufacturing;

our ability to enter into

and maintain collaborative, licensing and other commercial relationships;

and our partners’ commitment of time and resources to

the development and commercialization of our products.

if we can raise additional funding, we may be required to do so on terms that are dilutive to you.

capital markets have been unpredictable in the recent past for unprofitable companies such as ours.

The amount of capital that a company

such as ours is able to raise often depends on variables that are beyond our control.

As a result, we may not be able to secure financing

on terms attractive to us, or at all.

If we are able to consummate a financing arrangement, the amount raised may not be sufficient to

meet our future needs.

If adequate funds are not available on acceptable terms, or at all, our business, including our results of operations,

financial condition and our continued viability will be materially adversely affected.

Related to Product Development, Regulatory Approval, Manufacturing and Commercialization

are dependent upon the clinical success of our licensed products and technologies.

If we are unable to generate revenues from our licensed

products and technologies, our ability to create shareholder value may be limited.

do not currently generate revenues from any of our product candidates, and we may not be successful in obtaining regulatory approvals

to commence our clinical trials.

If we do not obtain such approvals, the time in which we expect to commence clinical programs for our

product candidates will be extended and such extension may increase our expenses and our need for additional capital.

Moreover, there

is no guarantee that our clinical trials will be successful or that we will continue clinical development in support of an approval from

the regulatory agencies for any indication.

We note that most drug candidates never reach the clinical stage and even those that do commence

clinical development have only a small chance of successfully completing clinical development and gaining regulatory approval.

our business currently depends entirely on the successful development, regulatory approval and commercialization of our product candidates,

which may never occur.

we have entered into the Voltron Agreement pursuant to which we and HaloVax intend to jointly develop products to prevent COVID-19, no

assurance can be given as to when, if ever, we will be able to develop any products for such purpose and if developed that such products

will be successfully commercialized.

March 2020, we entered into the Voltron Agreement pursuant to which we and HaloVax will work to jointly develop potential products candidates

to prevent COVID-19;

however, no assurance can be given as to when, if ever, we will be able to develop any products for such purpose.

Furthermore, we are subject to risks including, but not limited to, the following with respect to the development of a treatment for

Emergency Use Authorization marketing approval processes of the FDA are lengthy, time consuming and inherently unpredictable, and we

cannot guarantee that we will ever have a marketable product;

may encounter substantial delays in completing our clinical studies which in turn will require additional costs, or we may fail to demonstrate

adequate safety and efficacy to the satisfaction of applicable regulatory authorities;

successful clinical studies may require the enrollment of large numbers of patients, and suitable patients may be difficult to identify

be commercially successful, physicians must be persuaded that using our products are effective alternatives to other existing therapies

and treatments;

may depend on third parties for manufacturing our proposed product candidates and any conflicts with such partners could delay or prevent

the development or commercialization of such product candidates;

third-party contract manufacturers upon whom we rely to formulate and manufacture our product candidates do not perform, fail to manufacture

according to our specifications or fail to comply with strict regulations, our clinical studies could be adversely affected and the development

of our product candidates could be delayed or terminated or we could incur significant additional expenses;

events involving our products may lead the FDA to delay or deny clearance for our products or result in product recalls that could harm

our reputation, business and financial results;

we fail to comply with healthcare regulations, we could face substantial enforcement actions, including civil and criminal penalties

and our business, operations and financial condition could be adversely affected.

our joint venture with HaloVax, LLC (“HaloVax”) is not successful or if we fail to realize the benefits we anticipate from

such joint venture, we may not be able to capitalize on the full market potential of our potential products.

March 2020, we entered into the Voltron Agreement to form a joint venture entity named HaloVax to jointly develop potential product candidates

for the prevention of the COVID-19.

Pursuant to the terms of the Voltron Agreement we are entitled to receive sales-based royalties at

low single digit percentages.

In addition, in 2020, we purchased 6% of HaloVax’s outstanding membership interests and shall contribute

proceeds of the development of products to prevent COVID-19.

If and to the extent we and HaloVax are unable to develop potential product

candidates for the prevention of COVID-19, we will not be entitled to any sale-based royalties and the value of our ownership interest

in HaloVax could decline in which case we may lose all or part of our investment in HaloVax.

While Voltron has agreed

to cooperate and use commercially reasonable efforts to exchange information and resources that will lead to the development activities

and established a Joint Development Committee consisting of seven members, two of which were selected by us, to plan, review, coordinate

and oversee the performance of the development activities and timelines with respect to development activities, we have limited contractual

rights to direct its activities.

Moreover, we will not have any other control with respect to the operations of HaloVax.

Therefore, HaloVax

will have a greater influence with respect to its commercialization efforts and other operations.

In general, our joint venture with HaloVax

subjects us to a number of related risks including that:

we may not receive sales-based royalties pursuant to the terms of the Voltron Agreement;

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if any product candidates are successfully developed that we will be able to commercialize such products upon terms mutually agreeable or beneficial to us and HaloVax.

The marketing approval process of the

FDA is lengthy, time consuming and inherently unpredictable, and if we are ultimately unable to obtain marketing approval for the

product candidates we intend to develop, our business may be substantially harmed.

None of the product candidates we intend to

develop have gained marketing authorization, approval or clearance in the U.S.

or elsewhere, and we cannot guarantee that we will

ever have marketable products.

Our business is substantially dependent on our ability to complete the development of, obtain marketing

approval for, and successfully commercialize our product candidates in a timely manner.

We cannot commercialize our product candidates

in the United States or elsewhere without first obtaining approval from regulatory agencies such as the FDA to market each product

Our product candidates could fail to receive marketing approval for many reasons, including among others:

If HT-005 is not commercialized by Zylö

or otherwise acquired by a third party, we may not be able to capitalize on the full market potential of our interests with respect

In December 2021, we licensed HT-005 back to Zylö

and are entitled to receive a low single digit percent of the net proceeds attributable to

the sale of HT-005 to a third party, a low single digit percent of the net proceeds from

the sale of HT-005 in the United States and Canada and their respective territories (collectively,

the “Territory”) and a low double digit percent of any royalty Zylö receives

through the sublicense to a third party based on the net sales of HT-005 in the Territory.

In connection with the license of HT-005 back

to Zylö, we acquired 100,000 shares of Zylö’s Class B common stock.

December 31, 2021, we own 220,000 shares of Zylö’s Class B common stock.

is unable to sell or otherwise commercialize HT-005, we will not be entitled to any proceeds or sale-based royalties and the value of

our ownership interest in Zylö could decline in which case we may lose all or part of our investment in Zylö.

The marketing approval process of the FDA

is lengthy, time consuming and inherently unpredictable, and if we are ultimately unable to obtain marketing approval for the product

candidates we intend to develop, our business may be substantially harmed.

None of the product candidates we intend to develop

have gained marketing authorization, approval or clearance in the U.S.

or elsewhere, and we cannot guarantee that we will ever have marketable

Our business is substantially dependent on our ability to complete the development of, obtain marketing approval for, and successfully

commercialize our product candidates in a timely manner.

We cannot commercialize our product candidates in the United States or elsewhere

without first obtaining approval from regulatory agencies such as the FDA to market each product candidate.

Our product candidates could

fail to receive marketing approval for many reasons, including among others:

the FDA or other regulatory agencies may disagree with the design or implementation of our clinical trials;

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In addition, the process of seeking regulatory

clearance or approval to market the product candidates we intend to develop is expensive and time consuming and, notwithstanding

the effort and expense incurred, clearance or approval is never guaranteed.

If we are not successful in obtaining timely clearance

or approval of our product candidates from the FDA or other foreign regulatory agencies, we may never be able to generate significant

revenue and may be forced to cease operations.

clearance or approval to market the product candidates we intend to develop is expensive and time consuming and, notwithstanding the effort

and expense incurred, clearance or approval is never guaranteed.

If we are not successful in obtaining timely clearance or approval of

our product candidates from the FDA or other foreign regulatory agencies, we may never be able to generate significant revenue and may

be forced to cease operations.

The NDA process is costly, lengthy and uncertain.

Any NDA application filed by us

will have to be supported by extensive data, including, but not limited to, technical, pre-clinical, clinical, manufacturing and

labeling data, to demonstrate to the FDA’s satisfaction the safety and efficacy of the product for its intended use.

Obtaining clearances or approvals from the

FDA and from regulatory agencies in other countries is an expensive and time consuming process and is uncertain as to outcome.

The FDA and other agencies could ask us to supplement our submissions, collect non-clinical data, conduct additional clinical trials

or engage in other time-consuming actions, or it could simply deny our applications.

In addition, even if we obtain an NDA approval

or pre-market approvals in other countries, the approval could be revoked or other restrictions imposed if post-market data demonstrates

safety issues or lack of effectiveness.

We cannot predict with certainty how, or when, the FDA or other regulatory agencies will

If we are unable to obtain the necessary regulatory approvals, our financial condition and cash flow may be adversely affected,

and our ability to grow domestically and internationally may be limited.

Additionally, even if cleared or approved, our products

may not be approved for the specific indications that are most necessary or desirable for successful commercialization or profitability.

We may encounter substantial delays in

completing our clinical studies which in turn will require additional costs, or we may fail to demonstrate adequate safety and

efficacy to the satisfaction of applicable regulatory authorities.

It is impossible to predict if or when any

of our product candidates will prove safe or effective in humans or will receive regulatory approval.

Before obtaining marketing

approval from regulatory authorities for the sale of our product candidates, we must conduct extensive clinical studies to demonstrate

the safety and efficacy of the product candidates in humans.

Clinical testing is expensive, time-consuming and uncertain as to

We cannot guarantee that any clinical studies will be conducted as planned or completed on schedule, if at all.

of one or more clinical studies can occur at any stage of testing.

Events that may prevent successful or timely completion of clinical

development include:

Any NDA application filed by us will have to be supported

by extensive data, including, but not limited to, technical, pre-clinical, clinical, manufacturing and labeling data, to demonstrate to

the FDA’s satisfaction the safety and efficacy of the product for its intended use.

Obtaining clearances or approvals from the FDA

and from regulatory agencies in other countries is an expensive and time-consuming process and is uncertain as to outcome.

other agencies could ask us to supplement our submissions, collect non-clinical data, conduct additional clinical trials or engage in

other time-consuming actions, or it could simply deny our applications.

In addition, even if we obtain an NDA approval or pre-market approvals

in other countries, the approval could be revoked or other restrictions imposed if post-market data demonstrates safety issues or lack

of effectiveness.

We cannot predict with certainty how, or when, the FDA or other regulatory agencies will act.

If we are unable to obtain

the necessary regulatory approvals, our financial condition and cash flow may be adversely affected, and our ability to grow domestically

and internationally may be limited.

Additionally, even if cleared or approved, our products may not be approved for the specific indications

that are most necessary or desirable for successful commercialization or profitability.

We may encounter substantial delays in completing

our clinical studies which in turn will require additional costs, or we may fail to demonstrate adequate safety and efficacy to the satisfaction

of applicable regulatory authorities.

It is impossible to predict if or when any of

our product candidates will prove safe or effective in humans or will receive regulatory approval.

Before obtaining marketing approval

from regulatory authorities for the sale of our product candidates, we must conduct extensive clinical studies to demonstrate the safety

and efficacy of the product candidates in humans.

Clinical testing is expensive, time-consuming and uncertain as to outcome.

guarantee that any clinical studies will be conducted as planned or completed on schedule, if at all.

A failure of one or more clinical

studies can occur at any stage of testing.

Events that may prevent successful or timely completion of clinical development include:

delays in reaching, or failing to reach, a consensus with regulatory agencies on study design;

delays in reaching, or failing to reach, agreement on acceptable terms with a sufficient number of prospective contract research organizations (“CROs”) and clinical study sites, the terms of which can be subject to extensive negotiation and may vary significantly among different CROs and trial sites;

delays in obtaining required IRB or Ethics Committee (“EC”) approval at each clinical study site;

delays in recruiting a sufficient number of suitable patients to participate in our clinical studies;

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failure by our CROs, other third parties or us to adhere to clinical study, regulatory or legal requirements;

failure to perform in accordance with the FDA’s GCPs or applicable regulatory guidelines in other countries;

failure to perform in accordance with the FDA’s GCP or applicable regulatory guidelines in other countries;

delays in the testing, validation, manufacturing and delivery of sufficient quantities of our product candidates to the clinical sites;

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changes in regulatory requirements and guidance that require amending or submitting new clinical protocols.

We could also encounter delays if a clinical

trial is suspended or terminated by us, by the IRBs or ECs of the institutions in which such trials are being conducted, by an

independent Safety Review Board for such trial or by the FDA, Therapeutics Goods Administration (“TGA”), European

Medicines Agency (“EMA”), or other regulatory authorities.

Such authorities may suspend or terminate a clinical trial

due to a number of factors, including failure to conduct the clinical trial in accordance with regulatory requirements or our clinical

protocols, inspection of the clinical trial operations or trial site by the FDA, TGA, or other regulatory authorities resulting

in the imposition of a clinical hold, unforeseen safety issues or adverse side effects, failure to demonstrate a benefit from using

a drug, changes in governmental regulations or administrative actions or lack of adequate funding to continue the clinical trial.

We could also encounter delays if a clinical trial

is suspended or terminated by us, by the IRBs or ECs of the institutions in which such trials are being conducted, by an independent Safety

Review Board for such trial or by the FDA, Therapeutics Goods Administration (“TGA”), European Medicines Agency (“EMA”),

or other regulatory authorities.

Such authorities may suspend or terminate a clinical trial due to a number of factors, including failure

to conduct the clinical trial in accordance with regulatory requirements or our clinical protocols, inspection of the clinical trial operations

or trial site by the FDA, TGA, or other regulatory authorities resulting in the imposition of a clinical hold, unforeseen safety issues

or adverse side effects, failure to demonstrate a benefit from using a drug, changes in governmental regulations or administrative actions

or lack of adequate funding to continue the clinical trial.

Any inability to successfully complete pre-clinical

and clinical development could result in additional costs to us or impair our ability to generate revenues from product sales,

regulatory and commercialization milestones and royalties.

In addition, if we make manufacturing or formulation changes to our

product candidates, we may need to conduct additional studies to bridge our modified product candidates to earlier versions.

Clinical study delays could also shorten any

periods during which we may have the exclusive right to commercialize our product candidates or allow our competitors to bring

products to market before we do, which could impair our ability to successfully commercialize our product candidates.

any delays in completing our clinical trials will increase our costs, slow down our product candidate development and approval

process and jeopardize our ability to commence product sales and generate revenues.

Any of these occurrences may significantly

harm our business, financial condition and prospects.

In addition, many of the factors that cause, or lead to, a delay in the commencement

or completion of clinical trials may also ultimately lead to the denial of regulatory approval of our product candidates.

and clinical development could result in additional costs to us or impair our ability to generate revenues from product sales, regulatory

and commercialization milestones and royalties.

In addition, if we make manufacturing or formulation changes to our product candidates,

we may need to conduct additional studies to bridge our modified product candidates to earlier versions.

Clinical study delays could also shorten any periods

during which we may have the exclusive right to commercialize our product candidates or allow our competitors to bring products to market

before we do, which could impair our ability to successfully commercialize our product candidates.

In addition, any delays in completing

our clinical trials will increase our costs, slow down our product candidate development and approval process and jeopardize our ability

to commence product sales and generate revenues.

Any of these occurrences may significantly harm our business, financial condition and

In addition, many of the factors that cause, or lead to, a delay in the commencement or completion of clinical trials may also

ultimately lead to the denial of regulatory approval of our product candidates.

The outcome of pre-clinical studies and early

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predict final results.

Further, pre-clinical and clinical data are often susceptible to various interpretations and analyses, and

many companies that have believed their product candidates performed satisfactorily in pre-clinical studies and clinical trials

have nonetheless failed to obtain marketing approval.

If the results of our clinical studies are inconclusive or if there are safety

concerns or adverse events associated with our other product candidates, we may:

Further, pre-clinical and clinical data are often susceptible to various interpretations and analyses, and many

companies that have believed their product candidates performed satisfactorily in pre-clinical studies and clinical trials have nonetheless

failed to obtain marketing approval.

If the results of our clinical studies are inconclusive or if there are safety concerns or adverse

events associated with our other product candidates, we may:

be delayed in obtaining marketing approval for our product candidates, if approved at all;

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experience damage to our reputation.

Additionally, our product candidates could

potentially cause other adverse events that have not yet been predicted.

The inclusion of ill patients in our clinical studies

may result in deaths or other adverse medical events due to other therapies or medications that such patients may be using.

described above, any of these events could prevent us from achieving or maintaining market acceptance of our product candidates

and impair our ability to commercialize our products.

Additionally, our product candidates could potentially

cause other adverse events that have not yet been predicted.

The inclusion of ill patients in our clinical studies may result in deaths

or other adverse medical events due to other therapies or medications that such patients may be using.

As described above, any of these

events could prevent us from achieving or maintaining market acceptance of our product candidates and impair our ability to commercialize

our products.

If we are not able to obtain any required

regulatory approvals for our product candidates, we will not be able to commercialize our product candidates and our ability to

generate revenue will be limited.

regulatory approvals for our product candidates, we will not be able to commercialize our product candidates and our ability to generate

revenue will be limited.

We must successfully complete clinical trials

for our product candidates before we can apply for marketing approval.

Even if we complete our clinical trials, it does not assure

marketing approval.

Even if we complete our clinical trials, it does not assure marketing

Our pre-clinical trials may be unsuccessful, which would materially harm our business.

Even if our initial

pre-clinical trials are successful, we are required to conduct clinical trials to establish our product candidates’

and efficacy, before a marketing application (NDA or BLA or their foreign equivalents) can be filed with the FDA, the EMA, or comparable

foreign regulatory authorities for marketing approval of our product candidates.

Clinical testing is expensive, is difficult

to design and implement, can take many years to complete and is uncertain as to outcome.

Success in early phases of pre-clinical

and clinical trials does not ensure that later clinical trials will be successful, and interim results of a clinical trial do not

necessarily predict final results.

Even if our initial pre-clinical trials

are successful, we are required to conduct clinical trials to establish our product candidates’ safety and efficacy, before a marketing

application (NDA or BLA or their foreign equivalents) can be filed with the FDA, the EMA, or comparable foreign regulatory authorities

for marketing approval of our product candidates.

Clinical testing is expensive, is difficult to

design and implement, can take many years to complete and is uncertain as to outcome.

Success in early phases of pre-clinical and clinical

trials does not ensure that later clinical trials will be successful, and interim results of a clinical trial do not necessarily predict

final results.

A failure of one or more of our clinical trials can occur at any stage of testing.

We may experience

numerous unforeseen events during, or as a result of, the clinical trial process that could delay or prevent our ability to receive

regulatory approval or commercialize our product candidates.

The research, testing, manufacturing, labeling, packaging, storage,

approval, sale, marketing, advertising and promotion, pricing, export, import and distribution of drug products are subject to

extensive regulation by the FDA, EMA, and other regulatory authorities in the United States, European Union, and other countries,

where regulations differ from country to country.

We are not permitted to market our product candidates as prescription pharmaceutical

products in the United States until we receive approval of an NDA from the FDA, or in any foreign countries until we receive the

requisite approval from such countries.

In the United States, the FDA generally requires the completion of clinical trials of each

drug to establish its safety and efficacy and extensive pharmaceutical development to ensure its quality before an NDA is approved.

We may experience numerous unforeseen

events during, or as a result of, the clinical trial process that could delay or prevent our ability to receive regulatory approval or

commercialize our product candidates.

The research, testing, manufacturing, labeling, packaging, storage, approval, sale, marketing, advertising

and promotion, pricing, export, import and distribution of drug products are subject to extensive regulation by the FDA, EMA, and other

regulatory authorities in the United States, European Union, and other countries, where regulations differ from country to country.

are not permitted to market our product candidates as prescription pharmaceutical products in the United States until we receive approval

of an NDA from the FDA, or in any foreign countries until we receive the requisite approval from such countries.

In the United States,

the FDA generally requires the completion of clinical trials of each drug to establish its safety and efficacy and extensive pharmaceutical

development to ensure its quality before an NDA is approved.

Regulatory authorities in other jurisdictions impose similar requirements.

Of the large number of drugs in development, only a

small percentage result in the submission of an NDA to the FDA or other regulatory authorities and even fewer are eventually approved

for commercialization.

We have not submitted an NDA to the FDA or comparable applications to other regulatory authorities.

development efforts for our product candidates, including regulatory approval, are not successful for their planned indications,

or if adequate demand for our product candidates is not generated, our business will be materially adversely affected.

Of the large number of drugs in development, only a small percentage result in the submission of an NDA to the FDA or other regulatory

authorities and even fewer are eventually approved for commercialization.

We have not submitted an NDA to the FDA or comparable applications

to other regulatory authorities.

If our development efforts for our product candidates, including regulatory approval, are not successful

for their planned indications, or if adequate demand for our product candidates is not generated, our business will be materially adversely

Our success depends on the receipt of regulatory

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the FDA, EMA, or comparable foreign regulatory authorities or IRBs or ECs may disagree with the design or implementation of our clinical trials;

we may not be able to provide acceptable evidence of our product candidates’

safety and efficacy;

we may not be able to provide acceptable evidence of our product candidates’ safety and efficacy;

the results of our clinical trials may not be satisfactory or may not meet the level of statistical or clinical significance required by the FDA, EMA, or other regulatory agencies for marketing approval;

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our failure to demonstrate to the satisfaction of the FDA, EMA, or comparable regulatory authorities that a product candidate is safe and effective for its proposed indication;

we may fail to demonstrate that a product candidate’s clinical and other benefits outweigh its safety risks;

immunogenicity might affect a product candidate’s efficacy and/or safety;

we may fail to demonstrate that a product candidate’s clinical and other benefits outweigh its safety risks;

immunogenicity might affect a product candidate’s efficacy and/or safety;

the FDA, EMA, or comparable foreign regulatory authorities may disagree with our interpretation of data from nonclinical studies or clinical trials;

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Failure to obtain regulatory approval for our

product candidates for the foregoing, or any other reasons, will prevent us from commercializing our product candidates, and our

ability to generate revenue will be materially impaired.

We cannot guarantee that regulators will agree with our assessment of

the results of the clinical trials we intend to conduct in the future or that such trials will be successful.

The FDA, EMA and

other regulators have substantial discretion in the approval process and may refuse to accept any application or may decide that

our data is insufficient for approval and require additional clinical trials, or pre-clinical or other studies.

In addition, varying

interpretations of the data obtained from pre-clinical and clinical testing could delay, limit or prevent regulatory approval of

our product candidates.

product candidates for the foregoing, or any other reasons, will prevent us from commercializing our product candidates, and our ability

to generate revenue will be materially impaired.

We cannot guarantee that regulators will agree with our assessment of the results of

the clinical trials we intend to conduct in the future or that such trials will be successful.

The FDA, EMA and other regulators have

substantial discretion in the approval process and may refuse to accept any application or may decide that our data is insufficient for

approval and require additional clinical trials, or pre-clinical or other studies.

In addition, varying interpretations of the data obtained

from pre-clinical and clinical testing could delay, limit or prevent regulatory approval of our product candidates.

We have only limited experience in filing the

applications necessary to gain regulatory approvals and expect to rely on consultants and third party CROs with expertise in this

area to assist us in this process.

Securing regulatory approvals to market a product requires the submission of pre-clinical, clinical,

and/or pharmacokinetic data, information about product manufacturing processes and inspection of facilities and supporting information

to the appropriate regulatory authorities for each therapeutic indication to establish a product candidate’s safety and efficacy

for each indication.

Our product candidates may prove to have undesirable or unintended side effects, toxicities or other characteristics

that may preclude us from obtaining regulatory approval or prevent or limit commercial use with respect to one or all intended

applications necessary to gain regulatory approvals and expect to rely on consultants and third party CROs with expertise in this area

to assist us in this process.

Securing regulatory approvals to market a product requires the submission of pre-clinical, clinical, and/or

pharmacokinetic data, information about product manufacturing processes and inspection of facilities and supporting information to the

appropriate regulatory authorities for each therapeutic indication to establish a product candidate’s safety and efficacy for each

Our product candidates may prove to have undesirable or unintended side effects, toxicities or other characteristics that

may preclude us from obtaining regulatory approval or prevent or limit commercial use with respect to one or all intended indications.

The process of obtaining regulatory approvals

is expensive, often takes many years, if approval is obtained at all, and can vary substantially based upon, among other things,

the type, complexity and novelty of the product candidates involved, the jurisdiction in which regulatory approval is sought and

the substantial discretion of the regulatory authorities.

Changes in regulatory approval policies during the development period,

changes in or the enactment of additional statutes or regulations, or changes in regulatory review for a submitted product application

may cause delays in the approval or rejection of an application.

Regulatory approval obtained in one jurisdiction does not necessarily

mean that a product candidate will receive regulatory approval in all jurisdictions in which we may seek approval, but the failure

to obtain approval in one jurisdiction may negatively impact our ability to seek approval in a different jurisdiction.

to obtain regulatory marketing approval for our product candidates in any indication will prevent us from commercializing our product

candidates, and our ability to generate revenue will be materially impaired.

is expensive, often takes many years, if approval is obtained at all, and can vary substantially based upon, among other things, the type,

complexity and novelty of the product candidates involved, the jurisdiction in which regulatory approval is sought and the substantial

discretion of the regulatory authorities.

Changes in regulatory approval policies during the development period, changes in or the enactment

of additional statutes or regulations, or changes in regulatory review for a submitted product application may cause delays in the approval

or rejection of an application.

Regulatory approval obtained in one jurisdiction does not necessarily mean that a product candidate will

receive regulatory approval in all jurisdictions in which we may seek approval, but the failure to obtain approval in one jurisdiction

may negatively impact our ability to seek approval in a different jurisdiction.

Failure to obtain regulatory marketing approval for our

product candidates in any indication will prevent us from commercializing our product candidates, and our ability to generate revenue

will be materially impaired.

If we are unable to submit an application

for product candidate approval under Section 505(b)(2) of the FDCA or if we are required to generate additional data related to

the safety and efficacy of a product candidate in order to obtain approval under Section 505(b)(2), we may be unable to meet our

anticipated development and commercialization timelines.

We may seek marketing authorization in the

United States under Section 505(b)(2) of the FDCA which permits use of a marketing application, referred to as a 505(b)(2) application,

where at least some of the information required for approval comes from studies not conducted by or for the applicant and for which

the applicant has not obtained a right of reference or use.

The FDA interprets this to mean that an applicant may rely for approval

on such data as that found in published literature or the FDA’s finding of safety or effectiveness, or both, of a previously

approved drug product owned by a third party.

There is no assurance that the FDA would find third-party data relied upon by us

in a 505(b)(2) application sufficient or adequate to support approval and may require us to generate additional data to support

the safety and efficacy of a product candidate.

Consequently, we may need to conduct substantial new research and development activities

beyond those we currently plan to conduct.

Such additional new research and development activities would be costly and time consuming

and there is no assurance that such data generated from such additional activities would be sufficient to obtain approval.

If the data to be relied upon in a 505(b)(2)

application is related to drug products previously approved by the FDA and covered by patents that are listed in the FDA’s

Orange Book, we would be required to submit with our 505(b)(2) application a Paragraph IV Certification in which we must certify

that we do not infringe the listed patents or that such patents are invalid or unenforceable, and provide notice to the patent

owner or the holder of the approved NDA.

The patent owner or NDA holder would have 45 days from receipt of the notification of

our Paragraph IV Certification to initiate a patent infringement action against us.

If an infringement action is initiated, the

approval of our NDA would be subject to a stay of up to 30 months or more while we defend against such a suit.

Approval of our

product candidates under Section 505(b)(2) may therefore be delayed until patent exclusivity expires or until we successfully challenge

the applicability of those patents to our product candidates.

Alternatively, we may elect to generate sufficient clinical data

so that we would no longer need to rely on third-party data, which would be costly and time consuming and there would be no assurance

that such data generated from such additional activities would be sufficient to obtain approval.

for product candidate approval under Section 505(b)(2) of the FDCA or if we are required to generate additional data related to the safety

and efficacy of a product candidate in order to obtain approval under Section 505(b)(2), we may be unable to meet our anticipated development

and commercialization timelines.

We may seek marketing authorization in the United

States under Section 505(b)(2) of the FDCA which permits use of a marketing application, referred to as a 505(b)(2) application, where

at least some of the information required for approval comes from studies not conducted by or for the applicant and for which the applicant

has not obtained a right of reference or use.

The FDA interprets this to mean that an applicant may rely for approval on such data as

that found in published literature or the FDA’s finding of safety or effectiveness, or both, of a previously approved drug product

owned by a third party.

There is no assurance that the FDA would find third-party data relied upon by us in a 505(b)(2) application sufficient

or adequate to support approval and may require us to generate additional data to support the safety and efficacy of a product candidate.

Consequently, we may need to conduct substantial new research and development activities beyond those we currently plan to conduct.

additional new research and development activities would be costly and time consuming and there is no assurance that such data generated

from such additional activities would be sufficient to obtain approval.

If the data to be relied upon in a 505(b)(2) application

is related to drug products previously approved by the FDA and covered by patents that are listed in the FDA’s Orange Book, we would

be required to submit with our 505(b)(2) application a Paragraph IV Certification in which we must certify that we do not infringe the

listed patents or that such patents are invalid or unenforceable, and provide notice to the patent owner or the holder of the approved

The patent owner or NDA holder would have 45 days from receipt of the notification of our Paragraph IV Certification to initiate

a patent infringement action against us.

If an infringement action is initiated, the approval of our NDA would be subject to a stay of

up to 30 months or more while we defend against such a suit.

Approval of our product candidates under Section 505(b)(2) may therefore

be delayed until patent exclusivity expires or until we successfully challenge the applicability of those patents to our product candidates.

Alternatively, we may elect to generate sufficient clinical data so that we would no longer need to rely on third-party data, which would

be costly and time consuming and there would be no assurance that such data generated from such additional activities would be sufficient

to obtain approval.

We may not be able to obtain shortened review

of our applications, and the FDA may not agree that a product candidate qualifies for marketing approval.

If we are required to

generate additional data to support approval, we may be unable to meet anticipated or reasonable development and commercialization

timelines, may be unable to generate the additional data at a reasonable cost, or at all, and may be unable to obtain marketing

If the FDA changes its interpretation of Section 505(b)(2) allowing reliance on data in a previously approved drug application

owned by a third party, or there is a change in the law affecting Section 505(b)(2), this could delay or even prevent the FDA from

approving any Section 505(b)(2) application that we submit.

If we are required to generate

additional data to support approval, we may be unable to meet anticipated or reasonable development and commercialization timelines, may

be unable to generate the additional data at a reasonable cost, or at all, and may be unable to obtain marketing approval.

changes its interpretation of Section 505(b)(2) allowing reliance on data in a previously approved drug application owned by a third party,

or there is a change in the law affecting Section 505(b)(2), this could delay or even prevent the FDA from approving any Section 505(b)(2)

application that we submit.

We may not be able to obtain or maintain

orphan drug designation or exclusivity for our product candidates.

Regulatory authorities in some jurisdictions,

including the United States, may designate drugs for relatively small patient populations as “orphan drugs.” Under the Orphan

Drug Act, the FDA may designate a drug candidate as an orphan drug if it is intended to treat a rare disease or condition, which is generally

defined as a patient population of fewer than 200,000 individuals in the United States, or if the disease or condition affects more than

200,000 individuals in the United States and there is no reasonable expectation that the cost of developing and making a drug product

available in the United States for the type of disease or condition will be recovered from sales of the product.

Orphan drug designation entitles a party to financial

incentives, such as opportunities for grant funding towards clinical trial costs, tax advantages and user-fee waivers.

Additionally, if

a product that has orphan designation subsequently receives the first FDA approval for the disease or condition for which it has such

designation, the product is entitled to orphan drug exclusivity.

This means that the FDA may not approve any other applications to market

the same drug or biological product for the same indication for seven years, except in certain circumstances, including proving clinical

superiority (i.e., another product is safer, more effective or makes a major contribution to patient care) to the product with orphan

Competitors, however, may receive approval of different products for the indication for which the orphan product has exclusivity,

or obtain approval for the same product but for a different indication than that for which the orphan product has exclusivity.

exclusive marketing rights in the United States may be limited if we seek approval for an indication broader than the orphan-designated

indication or may be lost if the FDA later determines that the request for designation was materially defective.

Modifications to our products may require

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and/or prior to marketing and sales.

If the FDA requires new clearances or approvals for a particular use or indication, we may

be required to conduct additional clinical studies, which would require additional expenditures and harm our operating results.

If the products are already being used for these new indications, we may also be subject to significant enforcement actions.

clinical trials and obtaining clearances and approvals can be a time consuming process, and delays in obtaining required future

clearances or approvals could adversely affect our ability to introduce new or enhanced products in a timely manner, which in turn

would harm our future growth.

Conducting successful clinical studies

may require the enrollment of large numbers of patients, and suitable patients may be difficult to identify and recruit.

If the FDA requires new clearances or approvals for a particular use or indication, we may be required

to conduct additional clinical studies, which would require additional expenditures and harm our operating results.

If the products are

already being used for these new indications, we may also be subject to significant enforcement actions.

Conducting clinical trials and

obtaining clearances and approvals can be a time-consuming process, and delays in obtaining required future clearances or approvals could

adversely affect our ability to introduce new or enhanced products in a timely manner, which in turn would harm our future growth.

Conducting successful clinical studies may

require the enrollment of large numbers of patients, and suitable patients may be difficult to identify and recruit.

Patient enrollment in clinical trials and completion

of patient participation and follow-up depends on many factors, including the size of the patient population;

the nature of the

trial protocol;

the nature of the trial

the attractiveness of, or the discomforts and risks associated with, the treatments received by enrolled subjects;

the availability of appropriate clinical trial investigators;

the availability

of appropriate clinical trial investigators;

support staff;

and proximity of patients to clinical sites;

to comply with the eligibility and exclusion criteria for participation in the clinical trial;

proximity of patients to clinical sites;

ability to comply with the eligibility

and exclusion criteria for participation in the clinical trial;

and patient compliance.

patients may be discouraged from enrolling in our clinical trials if the trial protocol requires them to undergo extensive post-treatment

procedures or follow-up to assess the safety and effectiveness of our product candidates or if they determine that the treatments

received under the trial protocols are not attractive or involve unacceptable risks or discomforts.

Patients may also not participate

in our clinical trials if they choose to participate in contemporaneous clinical trials of competitive products.

Additional delays to the completion of

clinical studies may result from modifications being made to the protocol during the clinical trial, if such modifications are

warranted and/or required by the occurrences in the given trial .

Each modification to the protocol during a

clinical trial has to be submitted to the FDA.

This could result in the delay or halt of a clinical trial while the modification

is evaluated.

In addition, depending on the quantity and nature of the changes made, the FDA could take the position that the data

generated by the clinical trial is not poolable because the same protocol was not used throughout the trial.

This might require

the enrollment of additional subjects, which could result in the extension of the clinical trial and the FDA delaying clearance

or approval of a product.

Any such delay could have a material adverse effect on our business and results of operations.

For example, patients may be discouraged from

enrolling in our clinical trials if the trial protocol requires them to undergo extensive post-treatment procedures or follow-up to assess

the safety and effectiveness of our product candidates or if they determine that the treatments received under the trial protocols are

not attractive or involve unacceptable risks or discomforts.

Patients may also not participate in our clinical trials if they choose to

participate in contemporaneous clinical trials of competitive products.

Additional delays to the completion of clinical

studies may result from modifications being made to the protocol during the clinical trial, if such modifications are warranted and/or

required by the occurrences in the given trial .

Each modification to the protocol during a clinical

trial has to be submitted to the FDA.

This could result in the delay or halt of a clinical trial while the modification is evaluated.

In addition, depending on the quantity and nature of the changes made, the FDA could take the position that the data generated by the

clinical trial is not poolable because the same protocol was not used throughout the trial.

This might require the enrollment of additional

subjects, which could result in the extension of the clinical trial and the FDA delaying clearance or approval of a product.

delay could have a material adverse effect on our business and results of operations.

There can be no assurance that the data

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There can be no assurance that the data generated

using modified protocols will be acceptable to the FDA or that if future modifications during the trial are necessary, that any

such modifications will be acceptable to the FDA.

If the FDA believes that its prior approval is required for a particular modification,

it can delay or halt a clinical trial while it evaluates additional information regarding the change.

using modified protocols will be acceptable to the FDA or that if future modifications during the trial are necessary, that any such modifications

will be acceptable to the FDA.

If the FDA believes that its prior approval is required for a particular modification, it can delay or

halt a clinical trial while it evaluates additional information regarding the change.

Serious injury or death resulting from a failure

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Even though an adverse event may not be the result of the failure of our drug candidate,

the FDA or an IRB could delay or halt a clinical trial for an indefinite period of time while an adverse event is reviewed, and

likely would do so in the event of multiple such events.

Any delay or termination of our current or

future clinical trials as a result of the risks summarized above, including delays in obtaining or maintaining required approvals

from IRBs, delays in patient enrollment, the failure of patients to continue to participate in a clinical trial, and delays or

termination of clinical trials as a result of protocol modifications or adverse events during the trials, may cause an increase

in costs and delays in the filing of any product submissions with the FDA, delay the approval and commercialization of our products

or result in the failure of the clinical trial, which could adversely affect our business, operating results and prospects.

the FDA or an IRB could delay or halt a clinical trial for an indefinite period of time while an adverse event is reviewed, and likely

would do so in the event of multiple such events.

Any delay or termination of our current or future

clinical trials as a result of the risks summarized above, including delays in obtaining or maintaining required approvals from IRBs,

delays in patient enrollment, the failure of patients to continue to participate in a clinical trial, and delays or termination of clinical

trials as a result of protocol modifications or adverse events during the trials, may cause an increase in costs and delays in the filing

of any product submissions with the FDA, delay the approval and commercialization of our products or result in the failure of the clinical

trial, which could adversely affect our business, operating results and prospects.

We rely on third parties to conduct our

clinical trials and to assist us with pre-clinical development.

If these third parties do not perform as contractually required

or expected, we may not be able to obtain regulatory approval for or commercialize our products.

We do not have the ability to independently

conduct our pre-clinical and clinical trials for our product candidates, and we must rely on third parties, such as CROs, medical

institutions, clinical investigators and contract laboratories to conduct such trials.

If these third parties do not successfully

carry out their contractual duties or regulatory obligations, meet expected deadlines or need to be replaced, or if the quality

or accuracy of the data they obtain is compromised due to the failure to adhere to our clinical protocols or regulatory requirements

or for other reasons, our pre-clinical development activities or clinical trials may be extended, delayed, suspended or terminated,

and we may not be able to obtain regulatory approval for, or successfully commercialize, our products on a timely basis, if at

Furthermore, our third-party clinical trial investigators may be delayed in conducting our clinical trials for reasons outside

of their control.

The occurrence of any of the foregoing may adversely affect our business, operating results and prospects.

The future results of our current or

future clinical trials may not support our product candidate claims or may result in the discovery of unexpected adverse side effects.

Even if our clinical trials are completed as

planned, we cannot be certain that their results will support our drug candidate claims or that the FDA or foreign regulatory agencies

will agree with our conclusions regarding them.

Success in pre-clinical studies and early clinical trials does not ensure that

later clinical trials will be successful, and we cannot be sure that the later trials will replicate the results of prior trials

and pre-clinical studies.

The clinical trial process may fail to demonstrate that our drug candidates are safe and effective for

the proposed indicated uses.

If the FDA or other regulatory agencies conclude that the clinical trials for any of our product candidates

has failed to demonstrate safety and effectiveness, we would not receive clearance from the FDA or other regulatory agencies to

market that product in the United States or internationally for the indications sought.

In addition, such an outcome could cause us

to abandon the product candidate and might delay development of other product candidates.

Any delay or termination of our clinical

trials will delay the filing of any product submissions with the FDA and, ultimately, our ability to commercialize our product

candidates and generate revenues.

It is also possible that patients enrolled in clinical trials will experience adverse side effects

that are not currently part of the product candidate’s profile.

In addition, our clinical trials may involve a relatively

small patient population.

Because of the small sample size, our results may not be indicative of future results.

If these third parties do not perform as contractually required or expected,

we may not be able to obtain regulatory approval for or commercialize our products.

We do not have the ability to independently conduct

our pre-clinical and clinical trials for our product candidates, and we must rely on third parties, such as CROs, medical institutions,

clinical investigators and contract laboratories to conduct such trials.

If these third parties do not successfully carry out their contractual

duties or regulatory obligations, meet expected deadlines or need to be replaced, or if the quality or accuracy of the data they obtain

is compromised due to the failure to adhere to our clinical protocols or regulatory requirements or for other reasons, our pre-clinical

development activities or clinical trials may be extended, delayed, suspended or terminated, and we may not be able to obtain regulatory

approval for, or successfully commercialize, our products on a timely basis, if at all.

Furthermore, our third-party clinical trial investigators

may be delayed in conducting our clinical trials for reasons outside of their control.

The occurrence of any of the foregoing may adversely

affect our business, operating results and prospects.

The future results of our current or future

clinical trials may not support our product candidate claims or may result in the discovery of unexpected adverse side effects.

Even if our clinical trials are completed as planned,

we cannot be certain that their results will support our drug candidate claims or that the FDA or foreign regulatory agencies will agree

with our conclusions regarding them.

Success in pre-clinical studies and early clinical trials does not ensure that later clinical trials

will be successful, and we cannot be sure that the later trials will replicate the results of prior trials and pre-clinical studies.

clinical trial process may fail to demonstrate that our drug candidates are safe and effective for the proposed indicated uses.

FDA or other regulatory agencies conclude that the clinical trials for any of our product candidates has failed to demonstrate safety

and effectiveness, we would not receive clearance from the FDA or other regulatory agencies to market that product in the United States

or internationally for the indications sought.

In addition, such an outcome could cause us to

abandon the product candidate and might delay development of other product candidates.

Any delay or termination of our clinical trials

will delay the filing of any product submissions with the FDA and, ultimately, our ability to commercialize our product candidates and

generate revenues.

It is also possible that patients enrolled in clinical trials will experience adverse side effects that are not currently

part of the product candidate’s profile.

In addition, our clinical trials may involve a relatively small patient population.

of the small sample size, our results may not be indicative of future results.

Even if our product candidates are approved

by regulatory authorities, if we or our suppliers fail to comply with ongoing FDA regulations or if we experience unanticipated

problems with our products, these products could be subject to restrictions or withdrawal from the market.

by regulatory authorities, if we or our suppliers fail to comply with ongoing FDA regulations or if we experience unanticipated problems

with our products, these products could be subject to restrictions or withdrawal from the market.

The manufacturing processes, reporting requirements,

post-approval clinical data and promotional activities for any product candidate for which we obtain regulatory approval will be

subject to continued regulatory review, oversight and periodic inspections by the FDA.

In particular, we and our suppliers are

required to comply with FDA’s Quality System Regulations and International Standards Organization (“ISO”) regulations

for the manufacture of our products and other regulations which cover the methods and documentation of the design, testing, production,

control, quality assurance, labeling, packaging, storage and shipping of any product for which we obtain clearance or approval.

Regulatory bodies, such as the FDA, enforce these regulations through periodic inspections.

The failure by us or one of our suppliers

to comply with applicable statutes and regulations administered by the FDA and other regulatory bodies, or the failure to timely

and adequately respond to any adverse inspectional observations or product safety issues, could result in, among other things,

enforcement actions by the FDA.

post-approval clinical data and promotional activities for any product candidate for which we obtain regulatory approval will be subject

to continued regulatory review, oversight and periodic inspections by the FDA.

In particular, we and our suppliers are required to comply

with FDA’s Quality System Regulations and International Standards Organization (“ISO”) regulations for the manufacture

of our products and other regulations which cover the methods and documentation of the design, testing, production, control, quality assurance,

labeling, packaging, storage and shipping of any product for which we obtain clearance or approval.

Regulatory bodies, such as the FDA,

enforce these regulations through periodic inspections.

The failure by us or one of our suppliers to comply with applicable statutes and

regulations administered by the FDA and other regulatory bodies, or the failure to timely and adequately respond to any adverse inspectional

observations or product safety issues, could result in, among other things, enforcement actions by the FDA.

If any of these actions were to occur it would

harm our reputation and cause our product sales and profitability to suffer and may prevent us from generating revenue.

our key component suppliers may not currently be or may not continue to be in compliance with all applicable regulatory requirements

which could result in our failure to produce our products on a timely basis and in the required quantities, if at all.

Even if regulatory clearance or approval of

a product is granted, such clearance or approval may be subject to limitations on the intended uses for which the product may be

marketed and reduce the potential to successfully commercialize the product and generate revenue from the product.

If the FDA determines

that the product promotional materials, labeling, training or other marketing or educational activities constitute promotion of

an unapproved use, it could request that we or our commercialization partners cease or modify our training or promotional materials

or subject us to regulatory enforcement actions.

It is also possible that other federal, state or foreign enforcement authorities

might take action if they consider such training or other promotional materials to constitute promotion of an unapproved use, which

could result in significant fines or penalties under other statutory authorities, such as laws prohibiting false claims for reimbursement.

In addition, we may be required to conduct

costly post-market testing and surveillance to monitor the safety or effectiveness of our products, and we must comply with adverse

event and pharmacovigilance reporting requirements, including the reporting of adverse events which occur in connection with, and

whether or not directly related to, our products.

Later discovery of previously unknown problems with our products, including unanticipated

adverse events or adverse events of unanticipated severity or frequency, manufacturing problems, or failure to comply with regulatory

requirements, may result in changes to labeling, restrictions on such products or manufacturing processes, withdrawal of the products

from the market, voluntary or mandatory recalls, a requirement to recall, replace or refund the cost of any product we manufacture

or distribute, fines, suspension of regulatory approvals, product seizures, injunctions or the imposition of civil or criminal

penalties which would adversely affect our business, operating results and prospects.

Furthermore, our

key component suppliers may not currently be or may not continue to be in compliance with all applicable regulatory requirements which

could result in our failure to produce our products on a timely basis and in the required quantities, if at all.

Even if regulatory clearance or approval of a

product is granted, such clearance or approval may be subject to limitations on the intended uses for which the product may be marketed

and reduce the potential to successfully commercialize the product and generate revenue from the product.

If the FDA determines that the

product promotional materials, labeling, training or other marketing or educational activities constitute promotion of an unapproved use,

it could request that we or our commercialization partners cease or modify our training or promotional materials or subject us to regulatory

enforcement actions.

It is also possible that other federal, state or foreign enforcement authorities might take action if they consider

such training or other promotional materials to constitute promotion of an unapproved use, which could result in significant fines or

penalties under other statutory authorities, such as laws prohibiting false claims for reimbursement.

In addition, we may be required to conduct costly

post-market testing and surveillance to monitor the safety or effectiveness of our products, and we must comply with adverse event and

pharmacovigilance reporting requirements, including the reporting of adverse events which occur in connection with, and whether or not

directly related to, our products.

Later discovery of previously unknown problems with our products, including unanticipated adverse events

or adverse events of unanticipated severity or frequency, manufacturing problems, or failure to comply with regulatory requirements, may

result in changes to labeling, restrictions on such products or manufacturing processes, withdrawal of the products from the market, voluntary

or mandatory recalls, a requirement to recall, replace or refund the cost of any product we manufacture or distribute, fines, suspension

of regulatory approvals, product seizures, injunctions or the imposition of civil or criminal penalties which would adversely affect our

business, operating results and prospects.

Our revenue stream will depend upon third-party

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The commercial success of our products in both

domestic and international markets will be substantially dependent on whether third-party coverage and reimbursement is available

for patients that use our products.

However, the availability of insurance coverage and reimbursement for newly approved therapies

is uncertain, and therefore, third-party coverage may be particularly difficult to obtain even if our products are approved by

the FDA as safe and efficacious.

Patients using existing approved therapies are generally reimbursed all or part of the product

cost by Medicare or other third-party payors.

Medicare, Medicaid, health maintenance organizations and other third-party payors

are increasingly attempting to contain healthcare costs by limiting both coverage and the level of reimbursement of new drugs,

and, as a result, they may not cover or provide adequate payment for these products.

Submission of applications for reimbursement

approval generally does not occur prior to the filing of an NDA for that product and may not be granted for as long as many months

after NDA approval.

In order to obtain reimbursement arrangements for these products, we or our commercialization partners may

have to agree to a net sales price lower than the net sales price we might charge in other sales channels.

The continuing efforts

of government and third-party payors to contain or reduce the costs of healthcare may limit our revenue.

Initial dependence on

the commercial success of our products may make our revenues particularly susceptible to any cost containment or reduction efforts.

domestic and international markets will be substantially dependent on whether third-party coverage and reimbursement is available for

patients that use our products.

However, the availability of insurance coverage and reimbursement for newly approved therapies is uncertain,

and therefore, third-party coverage may be particularly difficult to obtain even if our products are approved by the FDA as safe and efficacious.

Patients using existing approved therapies are generally reimbursed all or part of the product cost by Medicare or other third-party payors.

Medicare, Medicaid, health maintenance organizations and other third-party payors are increasingly attempting to contain healthcare costs

by limiting both coverage and the level of reimbursement of new drugs, and, as a result, they may not cover or provide adequate payment

for these products.

Submission of applications for reimbursement approval generally does not occur prior to the filing of an NDA for that

product and may not be granted for as long as many months after NDA approval.

In order to obtain reimbursement arrangements for these

products, we or our commercialization partners may have to agree to a net sales price lower than the net sales price we might charge in

other sales channels.

The continuing efforts of government and third-party payors to contain or reduce the costs of healthcare may limit

Initial dependence on the commercial success of our products may make our revenues particularly susceptible to any cost containment

or reduction efforts.

Current and future legislation may increase

the difficulty and cost for us to obtain marketing approval of and commercialize our product candidates and affect the prices we

may obtain for such product candidates.

the difficulty and cost for us to obtain marketing approval of and commercialize our product candidates and affect the prices we may obtain

for such product candidates.

In the United States and some foreign jurisdictions,

there have been a number of legislative and regulatory changes and proposed changes regarding the healthcare system that could

prevent or delay marketing approval for our product candidates, restrict or regulate post-approval activities and affect our ability

to profitably sell our product candidates.

Legislative and regulatory proposals have been made to expand post-approval requirements

and restrict sales and promotional activities for pharmaceutical products.

We do not know whether additional legislative changes

will be enacted, or whether the FDA regulations, guidance or interpretations will be changed, or what the impact of such changes

on the marketing approvals of our product candidates, if any, may be.

there have been a number of legislative and regulatory changes and proposed changes regarding the healthcare system that could prevent

or delay marketing approval for our product candidates, restrict or regulate post-approval activities and affect our ability to profitably

sell our product candidates.

Legislative and regulatory proposals have been made to expand post-approval requirements and restrict sales

and promotional activities for pharmaceutical products.

We do not know whether additional legislative changes will be enacted, or whether

the FDA regulations, guidance or interpretations will be changed, or what the impact of such changes on the marketing approvals of our

product candidates, if any, may be.

In addition, increased scrutiny by the U.S.

Congress of the

FDA’s approval process may significantly delay or prevent marketing approval, as well as subject us to more stringent product

labeling and post-marketing testing and other requirements.

Congress of the FDA’s approval process may significantly

delay or prevent marketing approval, as well as subject us to more stringent product labeling and post-marketing testing and other requirements.

In the United States, the Medicare Modernization

Act (“MMA”) changed the way Medicare covers and pays for pharmaceutical products.

The legislation expanded Medicare

coverage for drug purchases by the elderly and introduced a new reimbursement methodology based on average sales prices for drugs.

In addition, this legislation authorized Medicare Part D prescription drug plans to use formularies where they can limit the number

of drugs that will be covered in any therapeutic class.

As a result of this legislation and the expansion of federal coverage of

drug products, we expect that there will be additional pressure to contain and reduce costs.

These cost reduction initiatives and

other provisions of this legislation could decrease the coverage and price that we receive for our product candidates and could

seriously harm our business.

While the MMA applies only to drug benefits for Medicare beneficiaries, private payors often follow

Medicare coverage policy and payment limitations in setting their own reimbursement rates, and any reduction in reimbursement that

results from the MMA may result in a similar reduction in payments from private payors.

The Patient Protection and Affordable Care

Act, as amended by the Health Care and Education Affordability Reconciliation Act of 2010 (collectively, the “Health Care

Reform Law”) is a sweeping law intended to broaden access to health insurance, reduce or constrain the growth of healthcare

spending, enhance remedies against fraud and abuse, add new transparency requirements for healthcare and health insurance industries,

impose new taxes and fees on the health industry and impose additional health policy reforms.

The Health Care Reform Law revised

the definition of “average manufacturer price”

for reporting purposes, which could increase the amount of Medicaid

drug rebates to states.

Further, the law imposed a significant annual fee on companies that manufacture or import branded prescription

drug products.

The Health Care Reform Law remains subject

to legislative efforts to repeal, modify or delay the implementation of the law.

However, if the Health Care Reform Law is repealed

or modified, or if implementation of certain aspects of the Health Care Reform Law are delayed, such repeal, modification or delay

may materially adversely impact our business, strategies, prospects, operating results or financial condition.

We are unable to

predict the full impact of any repeal, modification or delay in the implementation of the Health Care Reform Law on us at this

Due to the substantial regulatory changes that will need to be implemented by the Centers for Medicare & Medicaid

Services and others, and the numerous processes required to implement these reforms, we cannot predict which healthcare initiatives

will be implemented at the federal or state level, the timing of any such reforms, or the effect such reforms or any other future

legislation or regulation will have on our business.

In addition, other legislative changes have

been proposed and adopted in the United States since the Health Care Reform Law was enacted.

We expect that additional federal

healthcare reform measures will be adopted in the future, any of which could limit the amounts that federal and state governments

will pay for healthcare products and services, and in turn could significantly reduce the projected value of certain development

projects and reduce or eliminate our profitability.

We are dependent on third parties for

manufacturing and marketing of our proposed product candidates.

If we are not able to secure favorable arrangements with such third

parties, our business and financial condition could be harmed.

We will not manufacture any of our proposed

product candidates for commercial sale nor do we have the resources necessary to do so.

In addition, we currently do not have the

capability to market our drug products ourselves.

In addition to our internal sales force efforts, we have contracted with and

intend to continue to contract with specialized manufacturing companies to manufacture our proposed product candidates and partner

with larger pharmaceutical companies for commercialization of our products.

In connection with our efforts to commercialize our

proposed product candidates, we will seek to secure favorable arrangements with third parties to distribute, promote, market and

sell our proposed product candidates.

If our internal sales force is unable to successfully distribute, market and promote our

product candidates and we are not able to secure favorable commercial terms or arrangements with third parties for the distribution,

marketing, promotion and sales of our proposed product candidates, we may have to retain promotional and marketing rights and seek

to develop the commercial resources necessary to promote or co-promote or co-market certain or all of our proposed drug candidates

to the appropriate channels of distribution in order to reach the specific medical market that we are targeting.

We may not be

able to enter into any partnering arrangements on this or any other basis.

If we are not able to secure favorable partnering arrangements,

or are unable to develop the appropriate resources necessary for the commercialization of our proposed product candidates, our

business and financial condition could be harmed.

In addition, we will have to hire additional employees or consultants, since

our current employees have limited experience in these areas.

Sufficient employees with relevant skills may not be available to

Any increase in the number of our employees would increase our expense level, and could have an adverse effect on our financial

In addition, we, or our potential commercial

partners, may not successfully introduce our proposed product candidates or such candidates may not achieve acceptance by patients,

health care providers and insurance companies.

Further, it is possible that we may not be able to secure arrangements to manufacture,

market, distribute, promote and sell our proposed product candidates at favorable commercial terms that would permit us to make

To the extent that corporate partners conduct clinical trials, we may not be able to control the design and conduct of

these clinical trials.

Act (“MMA”) changed the way Medicare covers and pays for pharmaceutical products.

The legislation expanded Medicare coverage

for drug purchases by the elderly and introduced a new reimbursement methodology based on average sales prices for drugs.

this legislation authorized Medicare Part D prescription drug plans to use formularies where they can limit the number of drugs that will

be covered in any therapeutic class.

As a result of this legislation and the expansion of federal coverage of drug products, we expect

that there will be additional pressure to contain and reduce costs.

These cost reduction initiatives and other provisions of this legislation

could decrease the coverage and price that we receive for our product candidates and could seriously harm our business.

While the MMA

applies only to drug benefits for Medicare beneficiaries, private payors often follow Medicare coverage policy and payment limitations

in setting their own reimbursement rates, and any reduction in reimbursement that results from the MMA may result in a similar reduction

in payments from private payors.

The Patient Protection and Affordable Care Act,

as amended by the Health Care and Education Affordability Reconciliation Act of 2010 (collectively, the “Health Care Reform Law”)

is a sweeping law intended to broaden access to health insurance, reduce or constrain the growth of healthcare spending, enhance remedies

against fraud and abuse, add new transparency requirements for healthcare and health insurance industries, impose new taxes and fees on

the health industry and impose additional health policy reforms.

The Health Care Reform Law revised the definition of “average manufacturer

price” for reporting purposes, which could increase the amount of Medicaid drug rebates to states.

Further, the law imposed a significant

annual fee on companies that manufacture or import branded prescription drug products.

The Health Care Reform Law remains subject to

legislative efforts to repeal, modify or delay the implementation of the law.

However, if the Health Care Reform Law is repealed or modified,

or if implementation of certain aspects of the Health Care Reform Law are delayed, such repeal, modification or delay may materially adversely

impact our business, strategies, prospects, operating results or financial condition.

We are unable to predict the full impact of any

repeal, modification or delay in the implementation of the Health Care Reform Law on us at this time.

Due to the substantial regulatory

changes that will need to be implemented by the Centers for Medicare & Medicaid Services and others, and the numerous processes

required to implement these reforms, we cannot predict which healthcare initiatives will be implemented at the federal or state level,

the timing of any such reforms, or the effect such reforms or any other future legislation or regulation will have on our business.

In addition, other legislative changes have been

proposed and adopted in the United States since the Health Care Reform Law was enacted.

We expect that additional federal healthcare reform

measures will be adopted in the future, any of which could limit the amounts that federal and state governments will pay for healthcare

products and services, and in turn could significantly reduce the projected value of certain development projects and reduce or eliminate

our profitability.

We are dependent on third parties for manufacturing

and marketing of our proposed product candidates.

If we are not able to secure favorable arrangements with such third parties, our business

and financial condition could be harmed.

We will not manufacture any of our proposed product

candidates for commercial sale nor do we have the resources necessary to do so.

In addition, we currently do not have the capability to

market our drug products ourselves.

In addition to our internal sales force efforts, we have contracted with and intend to continue to

contract with specialized manufacturing companies to manufacture our proposed product candidates and partner with larger pharmaceutical

companies for commercialization of our products.

In connection with our efforts to commercialize our proposed product candidates, we will

seek to secure favorable arrangements with third parties to distribute, promote, market and sell our proposed product candidates.

internal sales force is unable to successfully distribute, market and promote our product candidates and we are not able to secure favorable

commercial terms or arrangements with third parties for the distribution, marketing, promotion and sales of our proposed product candidates,

we may have to retain promotional and marketing rights and seek to develop the commercial resources necessary to promote or co-promote

or co-market certain or all of our proposed drug candidates to the appropriate channels of distribution in order to reach the specific

medical market that we are targeting.

We may not be able to enter into any partnering arrangements on this or any other basis.

not able to secure favorable partnering arrangements or are unable to develop the appropriate resources necessary for the commercialization

of our proposed product candidates, our business and financial condition could be harmed.

In addition, we will have to hire additional

employees or consultants, since our current employees have limited experience in these areas.

Sufficient employees with relevant skills

may not be available to us.

Any increase in the number of our employees would increase our expense level and could have an adverse effect

on our financial position.

In addition, we, or our potential commercial partners,

may not successfully introduce our proposed product candidates or such candidates may not achieve acceptance by patients, health care

providers and insurance companies.

Further, it is possible that we may not be able to secure arrangements to manufacture, market, distribute,

promote and sell our proposed product candidates at favorable commercial terms that would permit us to make a profit.

To the extent that

corporate partners conduct clinical trials, we may not be able to control the design and conduct of these clinical trials.

We may have conflicts with our partners

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We may have conflicts with our partners, such

as conflicts concerning the interpretation of pre-clinical or clinical data, the achievement of milestones, the interpretation

of contractual obligations, payments for services, development obligations or the ownership of intellectual property developed

during our collaboration.

If any conflicts arise with any of our partners, such partner may act in a manner that is adverse to

our best interests.

Any such disagreement could result in one or more of the following, each of which could delay or prevent the

development or commercialization of our product candidates, and in turn prevent us from generating revenues:

unwillingness on the

part of a partner to pay us milestone payments or royalties we believe are due to us under a collaboration;

uncertainty regarding

ownership of intellectual property rights arising from our collaborative activities, which could prevent us from entering into

additional collaborations;

unwillingness by the partner to cooperate in the development or manufacture of the product, including

providing us with product data or materials;

unwillingness on the part of a partner to keep us informed regarding the progress

of its development and commercialization activities or to permit public disclosure of the results of those activities;

of litigation or alternative dispute resolution options by either party to resolve the dispute;

or attempts by either party to

terminate the agreement.

Even if we receive regulatory approval

for any of our product candidates, we may not be able to successfully commercialize the product and the revenue that we generate

from its sales, if any, may be limited.

as conflicts concerning the interpretation of pre-clinical or clinical data, the achievement of milestones, the interpretation of contractual

obligations, payments for services, development obligations or the ownership of intellectual property developed during our collaboration.

If any conflicts arise with any of our partners, such partner may act in a manner that is averse to our best interests.

Any such disagreement

could result in one or more of the following, each of which could delay or prevent the development or commercialization of our product

candidates, and in turn prevent us from generating revenues:

unwillingness on the part of a partner to pay us milestone payments or royalties

we believe are due to us under a collaboration;

uncertainty regarding ownership of intellectual property rights arising from our collaborative

activities, which could prevent us from entering into additional collaborations;

unwillingness by the partner to cooperate in the development

or manufacture of the product, including providing us with product data or materials;

unwillingness on the part of a partner to keep us

informed regarding the progress of its development and commercialization activities or to permit public disclosure of the results of those

initiating of litigation or alternative dispute resolution options by either party to resolve the dispute;

or attempts by

either party to terminate the agreement.

Even if we receive regulatory approval for

any of our product candidates, we may not be able to successfully commercialize the product and the revenue that we generate from its

sales, if any, may be limited.

If approved for marketing, the commercial success

of our product candidates will depend upon each product’s acceptance by the medical community, including physicians, patients

and health care payors.

of our product candidates will depend upon each product’s acceptance by the medical community, including physicians, patients and

health care payors.

The degree of market acceptance for any of our product candidates will depend on a number of factors, including:

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the inclusion or omission of our product candidates in applicable therapeutic and vaccine guidelines;

the effectiveness of our own or any future collaborators’

sales and marketing strategies;

the effectiveness of our own or any future collaborators’ sales and marketing strategies;

limitations or warnings contained in approved labeling from regulatory authorities;

2 unchanged sentences

If any of our product candidates are approved,

but do not achieve an adequate level of acceptance by physicians, health care payors, and patients, we may not generate sufficient

revenue and we may not be able to achieve or sustain profitability.

Our efforts to educate the medical community and third-party

payors on the benefits of our product candidates may require significant resources and may never be successful.

but do not achieve an adequate level of acceptance by physicians, health care payors, and patients, we may not generate sufficient revenue

and we may not be able to achieve or sustain profitability.

Our efforts to educate the medical community and third-party payors on the

benefits of our product candidates may require significant resources and may never be successful.

In addition, even if we obtain regulatory approvals,

the timing or scope of any approvals may prohibit or reduce our ability to commercialize our product candidates successfully.

example, if the approval process takes too long, we may miss market opportunities thereby giving other companies the ability to

develop competing products or establish market dominance.

Any regulatory approval we ultimately obtain may be limited or subject

to restrictions or post-approval commitments that render our product candidates not commercially viable.

For example, regulatory

authorities may approve any of our product candidates for fewer or more limited indications than we request, may grant approval

contingent on the performance of costly post-marketing clinical trials, or may approve any of our product candidates with a label

that does not include the labeling claims necessary or desirable for the successful commercialization for that indication.

the FDA or comparable foreign regulatory authorities may place conditions on approvals or require risk management plans or a REMS

to assure the safe use of the drug.

If the FDA concludes a REMS is needed, the sponsor of the NDA must submit a proposed REMS.

if the approval process takes too long, we may miss market opportunities thereby giving other companies the ability to develop competing

products or establish market dominance.

Any regulatory approval we ultimately obtain may be limited or subject to restrictions or post-approval

commitments that render our product candidates not commercially viable.

For example, regulatory authorities may approve any of our product

candidates for fewer or more limited indications than we request, may grant approval contingent on the performance of costly post-marketing

clinical trials, or may approve any of our product candidates with a label that does not include the labeling claims necessary or desirable

for the successful commercialization for that indication.

Further, the FDA or comparable foreign regulatory authorities may place conditions

on approvals or require risk management plans or a REMS to assure the safe use of the drug.

If the FDA concludes a REMS is needed, the

sponsor of the NDA must submit a proposed REMS.

The FDA will not approve the NDA without an approved REMS, if required.

A REMS could include medication guides, physician communication

plans, or elements to assure safe use, such as restricted distribution methods, patient registries and other risk minimization

A REMS could include

medication guides, physician communication plans, or elements to assure safe use, such as restricted distribution methods, patient registries

and other risk minimization tools.

The FDA may also require a REMS for an approved product when new safety information emerges.

Any of these limitations on

approval or marketing could restrict the commercial promotion, distribution, prescription or dispensing of our product candidates.

Moreover, product approvals may be withdrawn for non-compliance with regulatory standards or if problems occur following the initial

marketing of the product.

these limitations on approval or marketing could restrict the commercial promotion, distribution, prescription or dispensing of our product

Moreover, product approvals may be withdrawn for non-compliance with regulatory standards or if problems occur following the

initial marketing of the product.

Any of the foregoing scenarios could materially harm the commercial success of our product candidates.

The FDA’s policy with respect to Emergency Use Authorizations

is evolving and may limit the ability for medical products, including , to be eligible for commercialization under an Emergency

Use Authorization.

We intend to submit applications to FDA for

Emergency Use Authorization (“EUA”) for our COVID-19 products.

The FDA has the authority to grant an EUA to allow

unapproved medical products to be used in an emergency to diagnose, treat or prevent serious or life-threatening diseases or conditions

during the COVID-19 public health emergency.

If we are granted an EUA for our COVID-19 products, we would be able to commercialize

the products prior to FDA clearance or approval.

However, the FDA does not have review deadlines with respect to such submissions

and, therefore, the timing of any approval of an EUA submission is uncertain.

We cannot guarantee that the FDA will review our

data in a timely manner, or that the FDA will accept the data when reviewed.

The FDA may decide that our data are insufficient

for an EUA and require additional pre-clinical, clinical or other studies and refuse to approve our application.

the FDA may revoke an EUA where it is determined that the public health emergency no longer exists or warrants such authorization,

and therefore we cannot predict how long any authorized EUA would remain in place.

Further, the FDA’s policy with respect

to EUAs related to COVID-19 is evolving and may in the future limit the ability for medical products, including our products,

to be eligible for an EUA.

Our products will face significant competition,

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to face, intense competition from large pharmaceutical companies, as well as academic and research institutions.

We compete in

an industry that is characterized by:

(i) rapid technological change, (ii) evolving industry standards, (iii) emerging competition

and (iv) new product introductions.

Our competitors have and may develop products and technologies that will compete with our products

and technologies.

Because several competing companies and institutions have greater financial resources than us, they may be able

(i) provide broader services and product lines, (ii) make greater investments in research and development and (iii) carry on

larger research and development initiatives.

Our competitors also have greater development capabilities than we do and have substantially

greater experience in undertaking pre-clinical and clinical testing of products, obtaining regulatory approvals, and manufacturing

and marketing pharmaceutical products.

They also have greater name recognition and better access to customers than us.

Adverse events involving our products

may lead the FDA or other regulatory agencies to delay or deny clearance for our products or result in product recalls that could

harm our reputation, business and financial results.

We compete in an industry

that is characterized by:

(i) rapid technological change, (ii) evolving industry standards, (iii) emerging competition and (iv) new product

introductions.

Our competitors have and may develop products and technologies that will compete with our products and technologies.

several competing companies and institutions have greater financial resources than us, they may be able to:

(i) provide broader services

and product lines, (ii) make greater investments in research and development and (iii) carry on larger research and development initiatives.

Our competitors also have greater development capabilities than we do and have substantially greater experience in undertaking pre-clinical

and clinical testing of products, obtaining regulatory approvals, and manufacturing and marketing pharmaceutical products.

They also have

greater name recognition and better access to customers than us.

Adverse events involving our products may

lead the FDA or other regulatory agencies to delay or deny clearance for our products or result in product recalls that could harm our

reputation, business and financial results.

Once a product receives clearance or approval,

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or defects in design or manufacture.

With respect to the FDA, the authority to require a recall must be based on an FDA finding

that there is a reasonable probability that the product would cause serious injury or death.

Manufacturers may, under their own

initiative, recall a product if any material deficiency in a product is found.

A government-mandated or voluntary recall by us

or one of our distributors could occur as a result of adverse side effects, impurities or other product contamination, manufacturing

errors, design or labeling defects or other deficiencies and issues.

Recalls of any of our products would divert managerial and

financial resources and have an adverse effect on our financial condition and results of operations.

In addition, the FDA requires

that certain classifications of recalls be reported to FDA within ten working days after the recall is initiated.

Companies are

required to maintain certain records of recalls, even if they are not reportable to the FDA.

We may initiate voluntary recalls

involving our products in the future that we determine do not require notification of the FDA.

If the FDA disagrees with our determinations,

they could require us to report those actions as recalls.

A future recall announcement could harm our reputation with customers

and negatively affect our sales.

In addition, the FDA could take enforcement action for failing to report the recalls when they

were conducted.

If we fail to comply with healthcare

regulations, we could face substantial enforcement actions, including civil and criminal penalties and our business, operations

and financial condition could be adversely affected.

We could be subject to healthcare fraud and

abuse laws and patient privacy laws of both the federal government and the states in which we conduct our business.

The laws include:

the federal healthcare program anti-kickback law, which prohibits, among other things, persons from soliciting, receiving or providing remuneration, directly or indirectly, to induce either the referral of an individual, for an item or service or the purchasing or ordering of a good or service, for which payment may be made under federal healthcare programs such as the Medicare and Medicaid programs;

the Omnibus Budget Reconciliation Act of

1993 (42 U.S.C.

1395nn) (the “Stark Law”) prohibit referrals by a physician of “designated health services”

which are payable, in whole or in part, by Medicare or Medicaid, to an entity in which the physician or the physician's immediate

family member has an investment interest or other financial relationship, subject to several exceptions.

The Stark Law also prohibits

billing for services rendered pursuant to a prohibited referral.

Several states have enacted laws similar to the Stark Law.

state laws may cover all (not just Medicare and Medicaid) patients.

Many federal healthcare reform proposals in the past few years

have attempted to expand the Stark Law to cover all patients as well.

If we violate the Stark Law, our financial results and operations

With respect to the FDA, the authority to require a recall must be based on an FDA finding that there

is a reasonable probability that the product would cause serious injury or death.

Manufacturers may, under their own initiative, recall

a product if any material deficiency in a product is found.

A government-mandated or voluntary recall by us or one of our distributors

could occur as a result of adverse side effects, impurities or other product contamination, manufacturing errors, design or labeling defects

or other deficiencies and issues.

Recalls of any of our products would divert managerial and financial resources and have an adverse effect

on our financial condition and results of operations.

In addition, the FDA requires that certain classifications of recalls be reported

to FDA within ten working days after the recall is initiated.

Companies are required to maintain certain records of recalls, even if they

are not reportable to the FDA.

We may initiate voluntary recalls involving our products in the future that we determine do not require

notification of the FDA.

If the FDA disagrees with our determinations, they could require us to report those actions as recalls.

recall announcement could harm our reputation with customers and negatively affect our sales.

In addition, the FDA could take enforcement

action for failing to report the recalls when they were conducted.

If we fail to comply with healthcare regulations,

we could face substantial enforcement actions, including civil and criminal penalties and our business, operations and financial condition

could be adversely affected.

Penalties for violations include denial of payment for the services, significant civil monetary penalties,

and exclusion from the Medicare and Medicaid programs.

federal false claims laws which prohibit, among other things, individuals or entities from knowingly presenting, or causing to be presented, claims for payment from Medicare, Medicaid, or other third-party payers that are false or fraudulent, and which may apply to entities like us which provide coding and billing information to customers;

the federal Health Insurance Portability and Accountability

Act of 1996, the Health Information and Technology for Economic and Clinical Health Act and their implementing regulations at 45

Parts 160, 162 and 164, as amended (“HIPAA”) which imposes certain requirements relating to the privacy, security

and transmission of protected health information which includes individually identifiable health information, demographic data,

medical histories and test results;

the FDCA which among other things, strictly regulates drug manufacturing and product marketing, prohibits manufacturers from marketing drug products for off-label use and regulates the distribution of drug samples;

state law equivalents of each of the above federal laws, such as, Stark Law, anti-kickback and false claims laws which may apply to items or services reimbursed by any third-party payer, including commercial insurers, and state laws governing the privacy and security of health information in certain circumstances, many of which differ from each other in significant ways and often are not preempted by federal laws, thus complicating compliance efforts.

If our operations are found to be in violation

of any of the laws described above or any governmental regulations that apply to us, we may be subject to penalties, including

civil and criminal penalties, damages, fines and the curtailment or restructuring of our operations.

Any penalties, damages, fines,

curtailment or restructuring of our operations could adversely affect our ability to operate our business and our financial results.

Although compliance programs can mitigate the risk of investigation and prosecution for violations of these laws, the risks cannot

be entirely eliminated.

Any action against us for violation of these laws, even if we successfully defend against it, could cause

us to incur significant legal expenses and divert management’s attention from the operation of our business.

Moreover, achieving

and sustaining compliance with applicable federal and state privacy, security and fraud laws may prove costly.

Sales of our product candidates, if approved, or any other future product candidate will be subject to healthcare regulation and enforcement

by the federal government and the states and foreign governments in which we might conduct our business.

The healthcare laws and regulations

that may affect our ability to operate include the following:

the federal Anti-Kickback Statute makes it illegal for any person or entity to knowingly and willfully, directly or indirectly, solicit, receive, offer, or pay any remuneration that is in exchange for or to induce the referral of business, including the purchase, order, lease of any good, facility, item or service for which payment may be made under a federal healthcare program, such as Medicare or Medicaid.

The term “remuneration” has been broadly interpreted to include anything of value.

federal false claims and false statement laws, including the federal civil False Claims Act and the Civil Monetary Penalties Law (“CMPL”), prohibits, among other things, any person or entity from knowingly presenting, or causing to be presented, for payment to, or approval by, federal programs, including Medicare and Medicaid, claims for items or services, including drugs, that are false or fraudulent;

HIPAA, created additional federal criminal statutes that prohibit among other actions, knowingly and willfully executing, or attempting to execute, a scheme to defraud any healthcare benefit program, including private third-party payors or making any false, fictitious or fraudulent statement in connection with the delivery of or payment for healthcare benefits, items or services;

HIPAA, as amended by the Health Information Technology for Economic and Clinical Health Act of 2009 and their implementing regulations, impose obligations on certain types of individuals and entities regarding the electronic exchange of information in common healthcare transactions, as well as standards relating to the privacy and security of individually identifiable health information;

The federal Physician Payments Sunshine Act requires certain manufacturers of drugs, devices, biologics and medical supplies for which payment is available under Medicare, Medicaid or the Children’s Health Insurance Program, with specific exceptions, to report annually to the Centers for Medicare & Medicaid Services information related to payments or other transfers of value made to physicians and teaching hospitals, as well as ownership and investment interests held by physicians and their immediate family members.

Also, many states have similar laws and regulations,

such as anti-kickback and false claims laws that may be broader in scope and may apply regardless of payor, in addition to items and services

reimbursed under Medicaid and other state programs.

Additionally, we may be subject to state laws that require pharmaceutical companies

to comply with the federal government’s and/or pharmaceutical industry’s voluntary compliance guidelines, state laws that

require drug manufacturers to report information related to payments and other transfers of value to physicians and other healthcare providers

or marketing expenditures, as well as state and foreign laws governing the privacy and security of health information, many of which differ

from each other in significant ways and often are not preempted by HIPAA.

The laws and regulations applicable to our business

are complex, changing and often subject to varying interpretations.

As a result, we may not be able to adhere to all applicable laws and

Any violation or alleged violation of any of these laws or regulations by us could have a material adverse effect on our

business, financial condition, cash flows and results of operations.

We may be a party to various lawsuits, demands, claims, qui

tam suits, government investigations and audits, of which any could result in, among other things, substantial financial penalties

or awards against us, reputational harm, termination of relationships or contracts related to our business, mandated refunds, substantial

payments made by us, required changes to our business practices, exclusion from future participation in Medicare and other healthcare

programs and possible criminal penalties.

If we are found in violation of applicable laws

or regulations, we could suffer severe consequences that would have a material adverse effect on our business, results of operations,

financial condition, cash flows, reputation and stock price, including:

suspension or termination of our participation in federal healthcare programs;

criminal or civil liability, fines, damages or monetary penalties for violations of healthcare fraud and abuse laws, including the federal False Claims Act, CMPL, and Anti-Kickback Statute;

enforcement actions by governmental agencies or claims for monetary damages by patients under federal or state patient privacy laws, including HIPAA;

repayment of amounts received in violation of law or applicable payment program requirements, and related monetary penalties;

mandated changes to our practices or procedures that materially increase operating expenses;

imposition of corporate integrity agreements that could subject us to ongoing audits and reporting requirements as well as increased scrutiny of our business practices;

termination of various relationships or contracts related to our business;

harm to our reputation which could negatively affect our business relationships, decrease our ability to attract or retain patients and physicians, decrease access to new business opportunities and impact our ability to obtain financing, among other things.

Responding to lawsuits and other proceedings as

well as defending ourselves in such matters will continue to require management’s attention and cause us to incur significant legal

It is also possible that criminal proceedings may be initiated against us or individuals in our business in connection with investigations

by the federal government.

Furthermore, to the extent that our product is sold in a foreign country,

we may be subject to similar foreign laws.

If a third-party contract manufacturing

organization (“CMO”) upon whom we rely to formulate and manufacture our product candidates does not perform, fails

to manufacture according to our specifications or fails to comply with strict regulations, our pre-clinical studies or clinical

trials could be adversely affected and the development of our product candidates could be delayed or terminated or we could incur

significant additional expenses.

We do not own or operate any manufacturing

organization (“CMO”) upon whom we rely to formulate and manufacture our product candidates does not perform, fails to manufacture

according to our specifications or fails to comply with strict regulations, our pre-clinical studies or clinical trials could be adversely

affected, and the development of our product candidates could be delayed or terminated or we could incur significant additional expenses.

We do not own or operate any manufacturing facilities.

We rely on and intend to continue to rely on CMOs to formulate and manufacture our pre-clinical and clinical materials.

Our reliance on a CMO exposes us to a number of risks, any of which could delay or prevent the completion of our pre-clinical studies

or clinical trials, or the regulatory approval or commercialization of our product candidates, result in higher costs, or deprive

us of potential product revenues.

Our reliance on

a CMO exposes us to a number of risks, any of which could delay or prevent the completion of our pre-clinical studies or clinical trials,

or the regulatory approval or commercialization of our product candidates, result in higher costs, or deprive us of potential product

Some of these risks include:

our CMO failing to develop an acceptable formulation to support later-stage clinical trials for, or the commercialization of, our product candidates;

our CMO failing to manufacture our product candidate according to our specifications, the FDA’s cGMP requirements, or otherwise manufacturing material that we or the FDA may deem to be unsuitable in our clinical trials;

our CMO being unable to increase the scale of, increase the capacity for, or reformulate the form of our product candidates.

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We cannot assure you that our CMO will be able to manufacture our product candidates at a suitable scale, or we will be able to find alternative manufacturers acceptable to us that can do so;

our CMO placing a priority on the manufacture of their own products, or other customers’

our CMO placing a priority on the manufacture of their own products, or other customers’ products;

our CMO failing to perform as agreed upon or not remain in business;

our CMO’s plants being closed as a result of regulatory sanctions, natural disasters, health epidemics or otherwise.

Manufacturers of pharmaceutical products are

subject to ongoing periodic inspections by the FDA, the U.S.

Drug Enforcement Administration and corresponding state and foreign

agencies to ensure strict compliance with FDA mandated cGMPs, other government regulations and corresponding foreign standards.

While we are obligated to audit their performance, we do not have control over our CMO’s compliance with these regulations

and standards.

Failure by any of our CMOs, or us, to comply with applicable regulations could result in sanctions being imposed

on us or the CMOs.

These sanctions may include fines, injunctions, civil penalties, failure of the government to grant pre-market

approval of drugs, delays, suspension or withdrawal of approvals, seizures or recalls of product, operating restrictions and criminal

prosecutions, any of which could significantly and adversely affect our business.

our CMO’s plants being closed as a result of regulatory sanctions, natural disasters, health epidemics or otherwise.

Manufacturers of pharmaceutical products are subject

to ongoing periodic inspections by the FDA, the U.S.

Drug Enforcement Administration and corresponding state and foreign agencies to ensure

strict compliance with FDA mandated cGMPs, other government regulations and corresponding foreign standards.

While we are obligated to

audit their performance, we do not have control over our CMO’s compliance with these regulations and standards.

Failure by any of

our CMOs, or us, to comply with applicable regulations could result in sanctions being imposed on us or the CMOs.

These sanctions may

include fines, injunctions, civil penalties, failure of the government to grant pre-market approval of drugs, delays, suspension or withdrawal

of approvals, seizures or recalls of product, operating restrictions and criminal prosecutions, any of which could significantly and adversely

affect our business.

In the event that we need to change our

CMOs, our pre-clinical studies, clinical trials or the commercialization of our product candidates could be delayed, adversely

affected or terminated, or such a change may result in significantly higher costs.

CMOs, our pre-clinical studies, clinical trials or the commercialization of our product candidates could be delayed, adversely affected

or terminated, or such a change may result in significantly higher costs.

Various steps in the manufacture of our product

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produced by different manufacturers.

Changing our current or future CMOs may be difficult for us and could be costly, which could

result in our inability to manufacture our product candidates for an extended period of time and therefore a delay in the development

of our product candidates.

Further, in order to maintain our development time lines in the event of a change in our CMOs, we may

incur significantly higher costs to manufacture our product candidates.

Changing our current or future CMOs may be difficult for us and could be costly, which could result

in our inability to manufacture our product candidates for an extended period of time and therefore a delay in the development of our

product candidates.

Further, in order to maintain our development time lines in the event of a change in our CMOs, we may incur significantly

higher costs to manufacture our product candidates.

Healthcare Reform in the United States.

In the United States, there have been, and

continue to be, a number of legislative and regulatory changes and proposed changes to the healthcare system that could affect

the future results of pharmaceutical manufactures’

In particular, there have been and continue to be a number

of initiatives at the federal and state levels that seek to reduce healthcare costs.

Most recently, the Affordable Care Act (“ACA”) was enacted in March 2010, which includes measures to significantly change the way healthcare

is financed by both governmental and private insurers.

Among the provisions of the ACA of greatest importance to the pharmaceutical

and biotechnology industry are the following:

In the United States, there have been, and continue

to be, a number of legislative and regulatory changes and proposed changes to the healthcare system that could affect the future results

of pharmaceutical manufactures’ operations.

In particular, there have been and continue to be a number of initiatives at the federal

and state levels that seek to reduce healthcare costs.

On the federal level, the Affordable Care Act (“ACA”) was enacted in

March 2010, and included measures to significantly change the way healthcare is financed by both governmental and private insurers.

the provisions of the ACA that have been of greatest importance to the pharmaceutical and biotechnology industry are the following:

an annual, nondeductible fee on any entity that manufactures or imports certain branded prescription drugs and biologic agents, apportioned among these entities according to their market share in certain government healthcare programs;

implementation of the federal physician payment transparency requirements, sometimes referred to as the “Physician Payments Sunshine Act”;

a licensure framework for follow-on biologic products;

a new Patient-Centered Outcomes Research Institute to oversee, identify priorities in, and conduct comparative clinical effectiveness research, along with funding for such research;

creation of Patient-Centered Outcomes Research Institute to oversee, identify priorities in, and conduct comparative clinical effectiveness research, along with funding for such research;

establishment of a Center for Medicare Innovation at the Centers for Medicare & Medicaid Services to test innovative payment and service delivery models to lower Medicare and Medicaid spending, potentially including prescription drug spending;

an increase in the statutory minimum rebates a manufacturer must pay under the Medicaid Drug Rebate Program, to 23.1% and 13% of the average manufacturer price for most branded and generic drugs, respectively and capped the total rebate amount for innovator drugs at 100% of the Average Manufacturer Price;

a new methodology by which rebates owed by manufacturers under the Medicaid Drug Rebate Program are calculated for certain drugs and biologics, including our product candidates, that are inhaled, infused, instilled, implanted or injected;

extension of manufacturers’

Medicaid rebate liability to covered drugs dispensed to individuals who are enrolled in Medicaid managed care organizations;

expansion of eligibility criteria for Medicaid programs by, among other things, allowing states to offer Medicaid coverage to additional individuals and by adding new mandatory eligibility categories for individuals with income at or below 133% of the federal poverty level, thereby potentially increasing manufacturers’

Medicaid rebate liability;

a new Medicare Part D coverage gap discount program, in which manufacturers must agree to offer 50% point-of-sale discounts off negotiated prices of applicable brand drugs to eligible beneficiaries during their coverage gap period, as a condition for the manufacturer’s outpatient drugs to be covered under Medicare Part D;

adoption of methodology by which rebates owed by manufacturers under the Medicaid Drug Rebate Program are calculated for certain drugs and biologics, including our product candidates, that are inhaled, infused, instilled, implanted or injected;

extension of manufacturers’ Medicaid rebate liability to covered drugs dispensed to individuals who are enrolled in Medicaid managed care organizations;

creation of a Medicare Part D coverage gap discount program, in which manufacturers must agree to offer 50% point-of-sale discounts off negotiated prices of applicable brand drugs to eligible beneficiaries during their coverage gap period, as a condition for the manufacturer’s outpatient drugs to be covered under Medicare Part D;

expansion of the entities eligible for discounts under the Public Health program.

Some of the provisions of the ACA have

yet to be implemented, and there have been legal and political challenges to certain aspects of the ACA.

The Administration

has signed two executive orders and other directives designed to delay, circumvent, or loosen certain requirements mandated

Concurrently, Congress has considered legislation that would repeal or repeal and replace all or part of the

While Congress has not passed repeal legislation, the Tax Cuts and Jobs Act of 2017 includes a provision repealing,

effective January 1, 2019, the tax-based shared responsibility payment imposed by the ACA on certain individuals who fail

to maintain qualifying health coverage for all or part of a year that is commonly referred to as the “individual

mandate”.

Congress may consider other legislation to repeal or replace elements of the ACA.

Many of the details regarding the

implementation of the ACA are yet to be determined, and at this time, the full effect that the ACA would have on a

pharmaceutical manufacturer remains unclear.

This uncertainty is heightened by President Biden’s January 28, 2021

Executive Order on Strengthening Medicaid and the Affordable Care Act which indicates that the

incoming Biden Administration may significantly modify the ACA and potentially revoke any changes implemented by

the Trump Administration.

It is also possible that President Biden will further reform the ACA and other federal programs in

manner that may impact our operations.

The Biden Administration has indicated that a goal of its administration is to

expand and support Medicaid and the ACA and to make high-quality healthcare accessible and affordable.

The potential increase

in patients covered by government funded insurance may impact our pricing.

Further, it is possible that the Biden

Administration may further increase the scrutiny on drug pricing.

Additionally,

on December 14, 2018, a Texas U.S.

District Court Judge ruled that the ACA is unconstitutional in its entirety because the tax

penalty on certain individuals who fail to maintain qualifying health coverage for all or part of a year, commonly referred to

as the “individual mandate.”

Additionally, on December 18, 2019, the U.S.

Court of Appeals for the 5th Circuit ruled

that the individual mandate was unconstitutional and remanded the case back to the District Court to determine whether the remaining

provisions of the ACA are invalid as well.

The United States Supreme Court is currently reviewing this case, but it is unclear when

a decision will be made.

It is also unclear how the Supreme Court ruling, other such litigation and the healthcare reform measures

of the Biden administration will impact the ACA.

We cannot predict the likelihood, nature or extent of government regulation

that may arise from future legislation or administrative or executive action, either in the United States or abroad.

that additional state and federal health care reform measures will be adopted in the future, any of which could limit the amounts

that federal and state governments will pay for health care products and services.

Moreover, the Biden administration, including

his nominee for Secretary of DHHS, has indicated that lowering prescription drug prices is a priority, but we do not yet know what

steps the administration will take or whether such steps will be successful.

Although there have been legal and political challenges

to certain aspects of the ACA, the Biden Administration has affirmed support for the law, entered its own executive orders to enforce

and strengthen it, and committed to examining and, where appropriate, reversing contrary Trump Administration policies.

The Tax Cuts and

Jobs Act of 2017 includes a provision repealing, effective January 1, 2019, the tax-based shared responsibility payment imposed by the

ACA on certain individuals who fail to maintain qualifying health coverage for all or part of a year that is commonly referred to as the

“individual mandate.”

Because of the volatility surrounding the implementation

and enforcement of the ACA since its passage, and at this time, the full effect that the ACA would have on a pharmaceutical manufacturer

remains unclear.

This uncertainty is heightened by President Biden’s January 28, 2021 Executive Order on Strengthening Medicaid

and the Affordable Care Act which indicates that the Biden Administration may significantly modify the ACA and further reform the ACA

and other federal programs in manner that may impact our operations.

The Biden Administration has indicated that a goal of its administration

is to expand and support Medicaid and the ACA and to make high-quality healthcare accessible and affordable.

The potential increase in

patients covered by government funded insurance may impact our pricing.

Further, it is possible that the Biden Administration may further

increase scrutiny of drug pricing.

Additionally, in December 2019,

a federal appeals court held that the individual mandate portion of the ACA was

unconstitutional and left open the question whether the remaining provisions of

the ACA would be valid without the individual mandate.

However, on appeal, the Supreme

Court ruled in June 2021 that the parties challenging the law lacked standing, leaving the ACA in place.

is unclear how any other potential litigation challenging the ACA and the healthcare reform measures of the Biden administration will

impact the ACA.

We cannot predict the likelihood, nature or extent of government regulation that may arise from future legislation or

administrative or executive action, either in the United States or abroad.

We expect that additional state and federal health care reform

measures will be adopted in the future, any of which could limit the amounts that federal and state governments will pay for health care

products and services.

prescription drug pricing has been a recent focus of federal policymaking.

The Trump Administration issued a series of executive orders

and rules related to prescription drug pricing, including executive orders in July and September 2020 focused on reducing drug prices

and rules in November 2020 establishing a ‘Most Favored Nation’ rule tying Medicare Part B drug pricing to prices in other

countries, as well as a rule effectively banning rebates from Medicare Part D.

The Biden Administration has indicated that lowering prescription

drug prices is a priority for the Biden Administration as well.

Further, there is uncertainty surrounding the

applicability of the biosimilars provisions under the ACA.

The FDA has issued several guidance documents, but no implementing

regulations, on biosimilars.

The FDA has issued several guidance documents, but no implementing regulations,

on biosimilars.

A number of biosimilar applications have been approved over the past few years.

The regulations that

are ultimately promulgated and their implementation are likely to have considerable impact on the way pharmaceutical manufacturers

conduct their business and may require changes to current strategies.

A biosimilar is a biological product that is highly similar

to an approved drug notwithstanding minor differences in clinically inactive components, and for which there are no clinically

meaningful differences between the biological product and the approved drug in terms of the safety, purity, and potency of the

Individual states have become increasingly

aggressive in passing legislation and implementing regulations designed to control pharmaceutical and biological product pricing,

including price or patient reimbursement constraints, discounts, restrictions on certain product access, and marketing cost disclosure

and transparency measures, and to encourage importation from other countries and bulk purchasing.

Legally mandated price controls

on payment amounts by third-party payors or other restrictions could harm a pharmaceutical manufacturer’s business, results

of operations, financial condition and prospects.

In addition, regional healthcare authorities and individual hospitals are increasingly

using bidding procedures to determine what pharmaceutical products and which suppliers will be included in their prescription drug

and other healthcare programs.

This could reduce ultimate demand for certain products or put pressure product pricing, which could

negatively affect a pharmaceutical manufacturer’s business, results of operations, financial condition and prospects.

In addition, given recent federal and state

government initiatives directed at lowering the total cost of healthcare, Congress and state legislatures will likely continue

to focus on healthcare reform, the cost of prescription drugs and biologics and the reform of the Medicare and Medicaid programs.

While no one cannot predict the full outcome of any such legislation, it may result in decreased reimbursement for drugs and biologics,

which may further exacerbate industry-wide pressure to reduce prescription drug prices.

This could harm a pharmaceutical manufacturer’s

ability to generate revenue.

Increases in importation or re-importation of pharmaceutical products from foreign countries into

the United States could put competitive pressure on a pharmaceutical manufacturer’s ability to profitably price products,

which, in turn, could adversely affect business, results of operations, financial condition and prospects.

A pharmaceutical manufacturer

might elect not to seek approval for or market products in foreign jurisdictions in order to minimize the risk of re-importation,

which could also reduce the revenue generated from product sales.

It is also possible that other legislative proposals having similar

effects will be adopted.

Furthermore, regulatory authorities’

assessment of the data and results required to demonstrate safety and efficacy can change over time and can be affected by many

factors, such as the emergence of new information, including on other products, changing policies and agency funding, staffing

and leadership.

We cannot be sure whether future changes to the regulatory environment will be favorable or unfavorable to our

business prospects.

For example, average review times at the FDA for marketing approval applications can be affected by a variety

of factors, including budget and funding levels and statutory, regulatory and policy changes.

The regulations that are ultimately promulgated

and their implementation are likely to have considerable impact on the way pharmaceutical manufacturers conduct their business and may

require changes to current strategies.

A biosimilar is a biological product that is highly similar to an approved drug notwithstanding

minor differences in clinically inactive components, and for which there are no clinically meaningful differences between the biological

product and the approved drug in terms of the safety, purity, and potency of the product.

Individual states have become increasingly aggressive

in passing legislation and implementing regulations designed to control pharmaceutical and biological product pricing, including price

or patient reimbursement constraints, discounts, restrictions on certain product access, and marketing cost disclosure and transparency

measures, and to encourage importation from other countries and bulk purchasing.

Legally mandated price controls on payment amounts by

third-party payors or other restrictions could harm a pharmaceutical manufacturer’s business, results of operations, financial condition

and prospects.

In addition, regional healthcare authorities and individual hospitals are increasingly using bidding procedures to determine

what pharmaceutical products and which suppliers will be included in their prescription drug and other healthcare programs.

reduce ultimate demand for certain products or put pressure product pricing, which could negatively affect a pharmaceutical manufacturer’s

business, results of operations, financial condition and prospects.

In addition, given recent federal and state government

initiatives directed at lowering the total cost of healthcare, Congress and state legislatures will likely continue to focus on healthcare

reform, the cost of prescription drugs and biologics and the reform of the Medicare and Medicaid programs.

While no one cannot predict

the full outcome of any such legislation, it may result in decreased reimbursement for drugs and biologics, which may further exacerbate

industry-wide pressure to reduce prescription drug prices.

This could harm a pharmaceutical manufacturer’s ability to generate revenue.

Increases in importation or re-importation of pharmaceutical products from foreign countries into the United States could put competitive

pressure on a pharmaceutical manufacturer’s ability to profitably price products, which, in turn, could adversely affect business,

results of operations, financial condition and prospects.

A pharmaceutical manufacturer might elect not to seek approval for or market

products in foreign jurisdictions in order to minimize the risk of re-importation, which could also reduce the revenue generated from

product sales.

It is also possible that other legislative proposals having similar effects will be adopted.

Furthermore, regulatory authorities’ assessment

of the data and results required to demonstrate safety and efficacy can change over time and can be affected by many factors, such as

the emergence of new information, including on other products, changing policies and agency funding, staffing and leadership.

be sure whether future changes to the regulatory environment will be favorable or unfavorable to our business prospects.

average review times at the FDA for marketing approval applications can be affected by a variety of factors, including budget and funding

levels and statutory, regulatory and policy changes.

Security threats to our information technology

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It is essential to our business strategy that

our technology and network infrastructure and our physical buildings remain secure and are perceived by our customers and corporate

partners to be secure.

Despite security measures, however, any network infrastructure may be vulnerable to cyber-attacks by hackers

and other security threats.

We may face cyber-attacks that attempt to penetrate our network security, sabotage or otherwise disable

our research, products and services, misappropriate our or our customers’

and partners’

proprietary information, which

may include personally identifiable information, or cause interruptions of our internal systems and services.

Despite security

measures, we also cannot guarantee security of our physical buildings.

Physical building penetration or any cyber-attacks could

negatively affect our reputation, damage our network infrastructure and our ability to deploy our products and services, harm our

relationship with customers and partners that are affected, and expose us to financial liability.

Additionally, there are a number of state,

federal and international laws protecting the privacy and security of health information and personal data.

For example, HIPAA

imposes limitations on the use and disclosure of an individual’s healthcare information by healthcare providers, healthcare

clearinghouses, and health insurance plans, or, collectively, covered entities, and also grants individuals rights with respect

to their health information.

HIPAA also imposes compliance obligations and corresponding penalties for non-compliance on individuals

and entities that provide services to healthcare providers and other covered entities.

As part of the American Recovery and Reinvestment

Act of 2009 (“ARRA”) the privacy and security provisions of HIPAA were amended.

ARRA also made significant increases

in the penalties for improper use or disclosure of an individual’s health information under HIPAA and extended enforcement

authority to state attorneys general.

As amended by ARRA and subsequently by the final omnibus rule adopted in 2013, HIPAA also

imposes notification requirements on covered entities in the event that certain health information has been inappropriately accessed

or disclosed, notification requirements to individuals, federal regulators, and in some cases, notification to local and national

Notification is not required under HIPAA if the health information that is improperly used or disclosed is deemed secured

in accordance with encryption or other standards developed by the U.S.

Department of Health and Human Services.

Most states have

laws requiring notification of affected individuals and/or state regulators in the event of a breach of personal information, which

is a broader class of information than the health information protected by HIPAA.

Many state laws impose significant data security

requirements, such as encryption or mandatory contractual terms, to ensure ongoing protection of personal information.

outside of the U.S.

our technology and network infrastructure and our physical buildings remain secure and are perceived by our customers and corporate partners

to be secure.

Despite security measures, however, any network infrastructure may be vulnerable to cyber-attacks by hackers and other security

We may face cyber-attacks that attempt to penetrate our network security, sabotage or otherwise disable our research, products

and services, misappropriate our or our customers’ and partners’ proprietary information, which may include personally identifiable

information, or cause interruptions of our internal systems and services.

Despite security measures, we also cannot guarantee security

of our physical buildings.

Physical building penetration or any cyber-attacks could negatively affect our reputation, damage our network

infrastructure and our ability to deploy our products and services, harm our relationship with customers and partners that are affected,

and expose us to financial liability.

Additionally, there are a number of state, federal

and international laws protecting the privacy and security of health information and personal data.

For example, HIPAA imposes limitations

on the use and disclosure of an individual’s healthcare information by healthcare providers, healthcare clearinghouses, and health

insurance plans, or, collectively, covered entities, and also grants individuals rights with respect to their health information.

also imposes compliance obligations and corresponding penalties for non-compliance on individuals and entities that provide services to

healthcare providers and other covered entities.

As part of the American Recovery and Reinvestment Act of 2009 (“ARRA”) the

privacy and security provisions of HIPAA were amended.

ARRA also made significant increases in the penalties for improper use or disclosure

of an individual’s health information under HIPAA and extended enforcement authority to state attorneys general.

As amended by ARRA

and subsequently by the final omnibus rule adopted in 2013, HIPAA also imposes notification requirements on covered entities in the event

that certain health information has been inappropriately accessed or disclosed, notification requirements to individuals, federal regulators,

and in some cases, notification to local and national media.

Notification is not required under HIPAA if the health information that is

improperly used or disclosed is deemed secured in accordance with encryption or other standards developed by the U.S.

Department of Health

and Human Services.

Most states have laws requiring notification of affected individuals and/or state regulators in the event of a breach

of personal information, which is a broader class of information than the health information protected by HIPAA.

Many state laws impose

significant data security requirements, such as encryption or mandatory contractual terms, to ensure ongoing protection of personal information.

Activities outside of the U.S.

implicate local and national data protection standards, impose additional compliance requirements and generate

additional risks of enforcement for non-compliance.

We may be required to expend significant capital and other resources to ensure

ongoing compliance with applicable privacy and data security laws, to protect against security breaches and hackers or to alleviate

problems caused by such breaches.

We may be required to expend significant capital and other resources to ensure ongoing

compliance with applicable privacy and data security laws, to protect against security breaches and hackers or to alleviate problems caused

by such breaches.

Risks Relating to Our Intellectual Property

We rely upon licenses granted to us by

various licensors, and if such licensors do not adequately defend such licenses, our business may be harmed.

We have entered into and may, in the future,

enter into license and sublicense agreements with respect to our product candidates.

We have limited control over the activities

of our licensors, and we rely upon our licensors to protect their intellectual property, including the patents covered by our licenses.

We cannot be certain that activities conducted by our licensors have been or will be conducted in compliance with applicable laws

and regulations.

Furthermore, we have no or limited control or input over whether, and in what manner, our licensors may enforce

or defend the patents that we license against a third-party.

Our licensors may defend the patents we license less vigorously than

if we had enforced or defended the patents ourselves.

Furthermore, our licensors may not necessarily seek enforcement in scenarios

in which we would feel that enforcement was in our best interests.

For example, our licensors may not enforce the patents against

a competitor of ours who is not a direct competitor of such licensor.

If our in-licensed intellectual property is found to be invalid

or unenforceable, then our licensors may not be able to enforce the patents against a competitor of ours.

Moreover, if we fail

to meet our obligations under our license agreements, the licensor may terminate the license agreement.

Furthermore, if we fail

to meet our obligations under our sublicense agreements or our sublicensor fails to meet its obligations to the licensor, such

licensor may terminate the license agreement thereby terminating our sublicense agreement.

Our business depends upon us securing

and protecting critical intellectual property.

We rely upon licenses granted to us by various

licensors, and if such licensors do not adequately defend such licenses, our business may be harmed.

We have entered into and may, in the future, enter

into license and sublicense agreements with respect to our product candidates.

We have limited control over the activities of our licensors,

and we rely upon our licensors to protect their intellectual property, including the patents covered by our licenses.

We cannot be certain

that activities conducted by our licensors have been or will be conducted in compliance with applicable laws and regulations.

we have no or limited control or input over whether, and in what manner, our licensors may enforce or defend the patents that we license

against a third-party.

Our licensors may defend the patents we license less vigorously than if we had enforced or defended the patents

Furthermore, our licensors may not necessarily seek enforcement in scenarios in which we would feel that enforcement was in

our best interests.

For example, our licensors may not enforce the patents against a competitor of ours who is not a direct competitor

of such licensor.

If our in-licensed intellectual property is found to be invalid or unenforceable, then our licensors may not be able

to enforce the patents against a competitor of ours.

Moreover, if we fail to meet our obligations under our license agreements, the licensor

may terminate the license agreement.

Furthermore, if we fail to meet our obligations under our sublicense agreements or our sublicensor

fails to meet its obligations to the licensor, such licensor may terminate the license agreement thereby terminating our sublicense agreement.

Our business depends upon us securing and

protecting critical intellectual property.

Although we do not own and only license intellectual

property, to the extent we develop intellectual property, our commercial success will depend in part on obtaining and maintaining

patent, trade secret, copyright and trademark protection of our technologies in the United States and other jurisdictions as well

as successfully enforcing and defending such intellectual property rights against third-party challenges.

We will only be able

to protect our intellectual property from unauthorized use by third parties to the extent that valid and enforceable intellectual

property protection, such as patents or trade secrets, cover them.

In particular, we place considerable emphasis on obtaining patent

and trade secret protection for significant new technologies, products and processes.

Furthermore, the degree of future protection

of our proprietary rights is uncertain because legal means afford only limited protection and may not adequately protect our rights

or permit us to gain or keep our competitive advantage.

Moreover, the degree of future protection of our proprietary rights is

uncertain for products that are currently in the early stages of development because we cannot predict which of these products

will ultimately reach the commercial market or whether the commercial versions of these products will incorporate proprietary technologies.

Patent positions in our industry are

highly uncertain and involve complex legal and factual questions.

property, to the extent we develop intellectual property, our commercial success will depend in part on obtaining and maintaining patent,

trade secret, copyright and trademark protection of our technologies in the United States and other jurisdictions as well as successfully

enforcing and defending such intellectual property rights against third-party challenges.

We will only be able to protect our intellectual

property from unauthorized use by third parties to the extent that valid and enforceable intellectual property protection, such as patents

or trade secrets, cover them.

In particular, we place considerable emphasis on obtaining patent and trade secret protection for significant

new technologies, products and processes.

Furthermore, the degree of future protection of our proprietary rights is uncertain because

legal means afford only limited protection and may not adequately protect our rights or permit us to gain or keep our competitive advantage.

Moreover, the degree of future protection of our proprietary rights is uncertain for products that are currently in the early stages of

development because we cannot predict which of these products will ultimately reach the commercial market or whether the commercial versions

of these products will incorporate proprietary technologies.

Patent positions in our industry are highly

uncertain and involve complex legal and factual questions.

Accordingly, we cannot predict the breadth of claims that may be allowed

or enforced in our patents or in third-party patents.

For example, we or our licensors might not have been the first to make the

inventions covered by our pending patent applications and issued patents, as applicable;

we or our licensors might not have been

the first to file patent applications for these inventions;

others may independently develop similar or alternative technologies

or duplicate any of our technologies;

it is possible that none of our pending patent applications or the pending patent applications

of our licensors will result in issued patents;

our issued patents and issued patents of our licensors may not provide a basis

for commercially viable technologies, or may not provide us with any competitive advantages, or may be challenged and invalidated

by third parties;

and, we may not develop additional proprietary technologies that are patentable.

As a result, our owned and licensed

patents may not be valid and we may not be able to obtain and enforce patents and to maintain trade secret protection for the full

commercial extent of our technology.

The extent to which we are unable to do so could materially harm our business.

Patent positions in our industry are highly uncertain

and involve complex legal and factual questions.

Accordingly, we cannot predict the breadth of claims that may be allowed or enforced

in our patents or in third-party patents.

For example, we or our licensors might not have been the first to make the inventions covered

by our pending patent applications and issued patents, as applicable;

we or our licensors might not have been the first to file patent

applications for these inventions;

others may independently develop similar or alternative technologies or duplicate any of our technologies;

it is possible that none of our pending patent applications or the pending patent applications of our licensors will result in issued

our issued patents and issued patents of our licensors may not provide a basis for commercially viable technologies, or may not

provide us with any competitive advantages, or may be challenged and invalidated by third parties;

and, we may not develop additional

proprietary technologies that are patentable.

As a result, our owned and licensed patents may not be valid, and we may not be able to

obtain and enforce patents and to maintain trade secret protection for the full commercial extent of our technology.

The extent to which

we are unable to do so could materially harm our business.

We or our licensors have applied for and will

continue to apply for patents for certain products.

Such applications may not result in the issuance of any patents, and any patents

now held or that may be issued may not provide us with adequate protection from competition.

Furthermore, it is possible that patents

issued or licensed to us may be challenged successfully.

In that event, if we have a preferred competitive position because of

such patents, any preferred position held by us would be lost.

If we are unable to secure or to continue to maintain a preferred

position, we could become subject to competition from the sale of generic products.

Failure to receive, inability to protect, or

expiration of our patents for medical use, manufacture, conjugation and labeling of any of our product candidates may adversely

affect our business and operations.

Such applications may not result in the issuance of any patents, and any patents now

held or that may be issued may not provide us with adequate protection from competition.

Furthermore, it is possible that patents issued

or licensed to us may be challenged successfully.

In that event, if we have a preferred competitive position because of such patents,

any preferred position held by us would be lost.

If we are unable to secure or to continue to maintain a preferred position, we could

become subject to competition from the sale of generic products.

Failure to receive, inability to protect, or expiration of our patents

for medical use, manufacture, conjugation and labeling of any of our product candidates may adversely affect our business and operations.

Patents issued or licensed to us may be infringed

by the products or processes of others.

The cost of enforcing our patent rights against infringers, if such enforcement is required,

could be significant, and we do not currently have the financial resources to fund such litigation.

Further, such litigation can

go on for years and the time demands could interfere with our normal operations.

There has been substantial litigation and other

proceedings regarding patent and other intellectual property rights in the pharmaceutical industry.

We may become a party to patent

litigation and other proceedings.

The cost of enforcing our patent rights against infringers, if such enforcement is required, could

be significant, and we do not currently have the financial resources to fund such litigation.

Further, such litigation can go on for years

and the time demands could interfere with our normal operations.

There has been substantial litigation and other proceedings regarding

patent and other intellectual property rights in the pharmaceutical industry.

We may become a party to patent litigation and other proceedings.

The cost to us of any patent litigation, even if resolved in our favor, could be substantial.

Some of our competitors may be able to sustain the costs of such litigation more effectively than we can because of their substantially

greater financial resources.

Litigation may also absorb significant management time.

Some of our competitors may be able to sustain

the costs of such litigation more effectively than we can because of their substantially greater financial resources.

Litigation may also

absorb significant management time.

Unpatented trade secrets, improvements, confidential

know-how and continuing technological innovation are important to our scientific and commercial success.

Although we attempt to

and will continue to attempt to protect our proprietary information through reliance on trade secret laws and the use of confidentiality

agreements with our corporate partners, collaborators, employees and consultants and other appropriate means, these measures may

not effectively prevent disclosure of our proprietary information, and, in any event, others may develop independently, or obtain

access to, the same or similar information.

Although we attempt to and will

continue to attempt to protect our proprietary information through reliance on trade secret laws and the use of confidentiality agreements

with our corporate partners, collaborators, employees and consultants and other appropriate means, these measures may not effectively

prevent disclosure of our proprietary information, and, in any event, others may develop independently, or obtain access to, the same

or similar information.

If we are found to be infringing on patents

or trade secrets owned by others, we may be forced to cease or alter our product development efforts, obtain a license to continue

the development or sale of our products, and/or pay damages.

or trade secrets owned by others, we may be forced to cease or alter our product development efforts, obtain a license to continue the

development or sale of our products, and/or pay damages.

Our manufacturing processes and potential products

may violate proprietary rights of patents that have been or may be granted to competitors, universities or others, or the trade

secrets of those persons and entities.

As the pharmaceutical industry expands and more patents are issued, the risk increases that

our processes and potential products may give rise to claims that they infringe the patents or trade secrets of others.

persons could bring legal actions against us claiming damages and seeking to enjoin clinical testing, manufacturing and marketing

of the affected product or process.

If any of these actions are successful, in addition to any potential liability for damages,

we could be required to obtain a license in order to continue to conduct clinical tests, manufacture or market the affected product

or use the affected process.

Required licenses may not be available on acceptable terms, if at all, and the results of litigation

are uncertain.

If we become involved in litigation or other proceedings, it could consume a substantial portion of our financial

resources and the efforts of our personnel.

Our ability to protect and enforce any

patents we may obtain does not guaranty that we will secure the right to commercialize such patents.

may violate proprietary rights of patents that have been or may be granted to competitors, universities or others, or the trade secrets

of those persons and entities.

As the pharmaceutical industry expands and more patents are issued, the risk increases that our processes

and potential products may give rise to claims that they infringe the patents or trade secrets of others.

These other persons could bring

legal actions against us claiming damages and seeking to enjoin clinical testing, manufacturing and marketing of the affected product

If any of these actions are successful, in addition to any potential liability for damages, we could be required to obtain

a license in order to continue to conduct clinical tests, manufacture or market the affected product or use the affected process.

licenses may not be available on acceptable terms, if at all, and the results of litigation are uncertain.

If we become involved in litigation

or other proceedings, it could consume a substantial portion of our financial resources and the efforts of our personnel.

Our ability to protect and enforce any patents

we may obtain does not guaranty that we will secure the right to commercialize such patents.

A patent is a limited monopoly right conferred

upon an inventor, and his successors in title, in return for the making and disclosing of a new and non-obvious invention.

monopoly is of limited duration but, while in force, allows the patent holder to prevent others from making and/or using his invention.

While a patent gives the holder this right to exclude others, it is not a license to commercialize the invention, where other permissions

may be required for permissible commercialization to occur.

For example, a drug cannot be marketed without the appropriate authorization

from the FDA, regardless of the existence of a patent covering the product.

Further, the invention, even if patented itself, cannot

be commercialized if it infringes the valid patent rights of another party.

We rely on confidentiality agreements

to protect our trade secrets.

If these agreements are breached by our employees or other parties, our trade secrets may become

known to our competitors.

This monopoly

is of limited duration but, while in force, allows the patent holder to prevent others from making and/or using his invention.

patent gives the holder this right to exclude others, it is not a license to commercialize the invention, where other permissions may

be required for permissible commercialization to occur.

For example, a drug cannot be marketed without the appropriate authorization from

the FDA, regardless of the existence of a patent covering the product.

Further, the invention, even if patented itself, cannot be commercialized

if it infringes the valid patent rights of another party.

We rely on confidentiality agreements to

protect our trade secrets.

If these agreements are breached by our employees or other parties, our trade secrets may become known to our

We rely on trade secrets which we seek to protect

through confidentiality agreements with our employees and other parties.

If these agreements are breached, our competitors may

obtain and use our trade secrets to gain a competitive advantage over us.

We may not have any remedies against our competitors

and any remedies that may be available to us may not be adequate to protect our business or compensate us for the damaging disclosure.

In addition, we may have to expend resources to protect our interests from possible infringement by others.

If these agreements are breached, our competitors may obtain

and use our trade secrets to gain a competitive advantage over us.

We may not have any remedies against our competitors and any remedies

that may be available to us may not be adequate to protect our business or compensate us for the damaging disclosure.

In addition, we

may have to expend resources to protect our interests from possible infringement by others.

Related Risks to the Company

We have expanded and may continue to

expand, our business through the acquisition of rights to new drug candidates that could disrupt our business, harm our financial

condition and may also dilute current shareholders’

ownership interests in our Company.

Our business strategy includes expanding our

products and capabilities, and we may seek acquisitions of additional drug candidates or technologies to do so.

Acquisitions involve

numerous risks, including substantial cash expenditures;

We have expanded and may continue to expand,

our business through the acquisition of rights to new drug candidates that could disrupt our business, harm our financial condition and

may also dilute current shareholders’ ownership interests in our Company.

Our business strategy includes expanding our products

and capabilities, and we may seek acquisitions of additional drug candidates or technologies to do so.

Acquisitions involve numerous risks,

including substantial cash expenditures;

potentially dilutive issuance of equity securities;

incurrence of debt

and contingent liabilities, some of which may be difficult or impossible to identify at the time of acquisition;

difficulties in

assimilating the acquired technologies or the operations of the acquired companies;

diverting our management’s attention

away from other business concerns;

risks of entering markets in which we have limited or no direct experience;

and the potential

loss of our key employees or key employees of the acquired companies.

incurrence of debt and contingent liabilities,

some of which may be difficult or impossible to identify at the time of acquisition;

difficulties in assimilating the acquired technologies

or the operations of the acquired companies;

diverting our management’s attention away from other business concerns;

risks of entering

markets in which we have limited or no direct experience;

and the potential loss of our key employees or key employees of the acquired

We cannot assure you that any acquisition will

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We may misjudge the value or worth of an acquired product, company or business.

In addition, our future success would depend in part on our ability to manage the rapid growth associated with acquisitions.

cannot assure you that we will be able to make the combination of our business with that of acquired products, businesses or companies

work or be successful.

Furthermore, the development or expansion of our business or any acquired products, business or companies

may require a substantial capital investment by us.

We may not have these necessary funds or they might not be available to us

on acceptable terms or at all.

We may also seek to raise funds by selling shares of our preferred or common stock, which could

dilute each current shareholder’s ownership interest in the Company.

our future success would depend in part on our ability to manage the rapid growth associated with acquisitions.

We cannot assure you that

we will be able to make the combination of our business with that of acquired products, businesses or companies work or be successful.

Furthermore, the development or expansion of our business or any acquired products, business or companies may require a substantial capital

investment by us.

We may not have these necessary funds or they might not be available to us on acceptable terms or at all.

seek to raise funds by selling shares of our preferred or common stock, which could dilute each current shareholder’s ownership

interest in the Company.

Any international operations we undertake

may subject us to risks inherent with operations outside of the United States.

We may seek to obtain market clearance for

in foreign markets that we deem to generate significant opportunities.

However, even with the cooperation of a commercialization

partner, conducting drug development in foreign countries involves inherent risks, including, but not limited to:

in staffing, funding and managing foreign operations;

We may seek to obtain market clearance for in

foreign markets that we deem to generate significant opportunities.

However, even with the cooperation of a commercialization partner,

conducting drug development in foreign countries involves inherent risks, including, but not limited to:

difficulties in staffing, funding

and managing foreign operations;

unexpected changes in regulatory requirements;

export restrictions;

and other trade barriers;

tariffs and other trade barriers;

difficulties in protecting, acquiring, enforcing and litigating intellectual property rights;

in currency exchange rates;

fluctuations in currency exchange rates;

and potentially adverse tax consequences.

If we were to experience any of the difficulties listed above,

or any other difficulties, our international development activities and our overall financial condition may suffer and cause us

to reduce or discontinue our international development and registration efforts.

We may not be successful in hiring and

retaining key employees, including executive officers.

Our future operations and successes depend

in large part upon the strength of our management team.

We rely heavily on the continued service of each member of our management

Accordingly, if any member of our management team were to terminate their employment with us, such departure may have a material

adverse effect on our business.

In addition, our future success depends on our ability to identify, attract, hire or engage, retain

and motivate other well-qualified financial, managerial, technical, clinical and regulatory personnel.

There can be no assurance

that these professionals will be available in the market, or that we will be able to retain existing professionals or to meet or

to continue to meet their compensation requirements.

Furthermore, the cost base in relation to such compensation, which may include

equity compensation, may increase significantly, which could have a material adverse effect on us.

Failure to establish and maintain

an effective management team and work force could adversely affect our ability to operate, grow and manage our business.

If we were to experience any of the difficulties listed above, or any other difficulties, our

international development activities and our overall financial condition may suffer and cause us to reduce or discontinue our international

development and registration efforts.

We may not be successful in hiring and retaining

key employees, including executive officers.

Our future operations and successes depend in

large part upon the strength of our management team.

We rely heavily on the continued service of each member of our management team.

if any member of our management team were to terminate their employment with us, such departure may have a material adverse effect on

our business.

In addition, our future success depends on our ability to identify, attract, hire or engage, retain and motivate other well-qualified

financial, managerial, technical, clinical and regulatory personnel.

There can be no assurance that these professionals will be available

in the market, or that we will be able to retain existing professionals or to meet or to continue to meet their compensation requirements.

Furthermore, the cost base in relation to such compensation, which may include equity compensation, may increase significantly, which

could have a material adverse effect on us.

Failure to establish and maintain an effective management team and work force could adversely

affect our ability to operate, grow and manage our business.

Managing our growth as we expand operations

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We expect to grow rapidly in order to support

additional, larger, and potentially international, pivotal clinical trials of our drug candidates, which will place a significant

strain on our financial, managerial and operational resources.

In order to achieve and manage growth effectively, we must continue

to improve and expand our operational and financial management capabilities.

Moreover, we will need to increase staffing and to

train, motivate and manage our employees.

All of these activities will increase our expenses and may require us to raise additional

capital sooner than expected.

additional, larger, and potentially international, pivotal clinical trials of our drug candidates, which will place a significant strain

on our financial, managerial and operational resources.

In order to achieve and manage growth effectively, we must continue to improve

and expand our operational and financial management capabilities.

Moreover, we will need to increase staffing and to train, motivate and

manage our employees.

All of these activities will increase our expenses and may require us to raise additional capital sooner than expected.

Failure to manage growth effectively could harm our business, financial condition or results of operations.

If a product liability claim is successfully

brought against us for uninsured liabilities, or such claim exceeds our insurance coverage, we could be forced to pay substantial

damage awards that could materially harm our business.

brought against us for uninsured liabilities, or such claim exceeds our insurance coverage, we could be forced to pay substantial damage

awards that could materially harm our business.

The use of any of our existing or future product

candidates in clinical trials and the sale of any approved pharmaceutical products may expose us to significant product liability

candidates in clinical trials and the sale of any approved pharmaceutical products may expose us to significant product liability claims.

We currently do not have product liability insurance coverage but we intend to obtain such insurance.

Such insurance coverage

may not protect us against any or all of the product liability claims that may be brought against us in the future.

be able to acquire or maintain adequate product liability insurance coverage at a commercially reasonable cost or in sufficient

amounts or scope to protect us against potential losses.

In the event a product liability claim is brought against us, we may be

required to pay legal and other expenses to defend the claim, as well as uncovered damage awards resulting from a claim brought

successfully against us.

In the event our product candidate is approved for sale by the FDA or other regulatory agency and commercialized,

we may need to substantially increase the amount of our product liability coverage.

Defending any product liability claim or claims

could require us to expend significant financial and managerial resources, which could have an adverse effect on our business.

Such insurance coverage may not

protect us against any or all of the product liability claims that may be brought against us in the future.

We may not be able to acquire

or maintain adequate product liability insurance coverage at a commercially reasonable cost or in sufficient amounts or scope to protect

us against potential losses.

In the event a product liability claim is brought against us, we may be required to pay legal and other expenses

to defend the claim, as well as uncovered damage awards resulting from a claim brought successfully against us.

In the event our product

candidate is approved for sale by the FDA or other regulatory agency and commercialized, we may need to substantially increase the amount

of our product liability coverage.

Defending any product liability claim or claims could require us to expend significant financial and

managerial resources, which could have an adverse effect on our business.

Our business may be adversely affected

by the ongoing coronavirus pandemic.

The outbreak of the

novel Coronavirus (COVID-19) evolved into a global pandemic.

The outbreak of the novel

Coronavirus (COVID-19) evolved into a global pandemic.

The coronavirus has spread to many regions of the world.

to which the coronavirus impacts our business and operating results will depend on future developments that are highly uncertain

and cannot be accurately predicted, including new information that may emerge concerning the coronavirus and the actions to contain

the coronavirus or treat its impact, among others.

The extent to which the

coronavirus impacts our business and operating results will depend on future developments that are highly uncertain and cannot be accurately

predicted, including new information that may emerge concerning the coronavirus, including variants, and the actions to contain the coronavirus

or treat its impact, among others.

Should the coronavirus

continue to spread, our business operations could be delayed or interrupted.

For instance, our clinical trials may be affected

by the pandemic.

Site initiation, participant recruitment and enrollment, participant dosing, distribution of clinical trial materials,

study monitoring and data analysis may be paused or delayed due to changes in hospital or university policies, federal, state or

local regulations, prioritization of hospital resources toward pandemic efforts, or other reasons related to the pandemic.

coronavirus continues to spread, some participants and clinical investigators may not be able to comply with clinical trial protocols.

For example, quarantines or other travel limitations (whether voluntary or required) may impede participant movement, affect sponsor

access to study sites, or interrupt healthcare services, and we may be unable to conduct our clinical trials.

Further, if the spread

of the coronavirus pandemic continues and our operations are adversely impacted, we risk a delay, default and/or nonperformance

under existing agreements which may increase our costs.

These cost increases may not be fully recoverable or adequately covered

by insurance.

For instance, our clinical trials may be affected by the

Site initiation, participant recruitment and enrollment, participant dosing, distribution of clinical trial materials, study

monitoring and data analysis may be paused or delayed due to changes in hospital or university policies, federal, state or local regulations,

prioritization of hospital resources toward pandemic efforts, or other reasons related to the pandemic.

If the coronavirus continues to

spread, some participants and clinical investigators may not be able to comply with clinical trial protocols.

For example, quarantines

or other travel limitations (whether voluntary or required) may impede participant movement, affect sponsor access to study sites, or

interrupt healthcare services, and we may be unable to conduct our clinical trials.

Further, if the spread of the coronavirus pandemic

continues and our operations are adversely impacted, we risk a delay, default and/or nonperformance under existing agreements which may

increase our costs.

These cost increases may not be fully recoverable or adequately covered by insurance.

Infections and deaths

related to the pandemic may disrupt the United States’

healthcare and healthcare regulatory systems.

Such disruptions could

divert healthcare resources away from, or materially delay FDA review and/or approval with respect to, our clinical trials.

is unknown how long these disruptions could continue, were they to occur.

Any elongation or de-prioritization of our

clinical trials or delay in regulatory review resulting from such disruptions could materially affect the development and study

of our product candidates.

related to the pandemic may disrupt the United States’ healthcare and healthcare regulatory systems.

Such disruptions could divert

healthcare resources away from, or materially delay FDA review and/or approval with respect to, our clinical trials.

It is unknown how

long these disruptions could continue, were they to occur.

Any elongation or de-prioritization of our clinical trials or delay

in regulatory review resulting from such disruptions could materially affect the development and study of our product candidates.

We currently utilize

third parties to, among other things, manufacture raw materials.

If either any third-party parties in the supply chain for materials

used in the production of our product candidates are adversely impacted by restrictions resulting from the coronavirus outbreak,

our supply chain may be disrupted, limiting our ability to manufacture our product candidates for our clinical trials and research

and development operations.

If any third parties in the supply chain for materials used in the production

of our product candidates are adversely impacted by restrictions resulting from the coronavirus outbreak, our supply chain may be disrupted,

limiting our ability to manufacture our product candidates for our clinical trials and research and development operations.

In the event of a shelter-in-place order

or other mandated local travel restrictions, our employees conducting research and development or manufacturing activities may

not be able to access their laboratory or manufacturing space, and our core activities may be significantly limited or curtailed,

possibly for an extended period of time.

The spread of the

coronavirus, which has caused a broad impact globally, including restrictions on travel and quarantine policies put into place

by businesses and governments, may have a material economic effect on our business.

While the potential economic impact brought

by and the duration of the pandemic may be difficult to assess or predict, it has already caused, and is likely to result in further,

significant disruption of global financial markets, which may reduce our ability to access capital either at all or on favorable

In addition, a recession, depression or other sustained adverse market event resulting from the spread of the coronavirus

could materially and adversely affect our business and the value of our common stock.

The ultimate impact

of the current pandemic, or any other health epidemic, is highly uncertain and subject to change.

We do not yet know the full extent

of potential delays or impacts on our business, our clinical trials, our research programs, healthcare systems or the global economy

However, these effects could have a material impact on our operations, and we will continue to monitor the situation

or other mandated local travel restrictions, our employees conducting research and development, or manufacturing activities may not be

able to access their laboratory or manufacturing space, and our core activities may be significantly limited or curtailed, possibly for

an extended period of time.

The spread of the coronavirus,

which has caused a broad impact globally, including restrictions on travel and quarantine policies put into place by businesses and governments,

may have a material economic effect on our business.

While the potential economic impact brought by and the duration of the pandemic may

be difficult to assess or predict, it has already caused, and is likely to result in further, significant disruption of global financial

markets, which may reduce our ability to access capital either at all or on favorable terms.

In addition, a recession, depression or other

sustained adverse market event resulting from the spread of the coronavirus could materially and adversely affect our business and the

value of our common stock.

The ultimate impact of

the current pandemic, or any other health epidemic, is highly uncertain and subject to change.

We do not yet know the full extent of potential

delays or impacts on our business, our clinical trials, our research programs, healthcare systems or the global economy as a whole.

these effects could have a material impact on our operations, and we will continue to monitor the situation closely.

Risks Related to Our Common Stock

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You should consider an investment in our common

stock to be risky, and you should invest in our common stock only if you can withstand a significant loss and wide fluctuations

in the market value of your investment.

Some factors that may cause the market price of our common stock to fluctuate, in addition

to the other risks mentioned in this “Risk Factors”

section and elsewhere in this Annual Report on Form 10-K, are:

stock to be risky, and you should invest in our common stock only if you can withstand a significant loss and wide fluctuations in the

market value of your investment.

Some factors that may cause the market price of our common stock to fluctuate, in addition to the other

risks mentioned in this “Risk Factors” section and elsewhere in this Annual Report on Form 10-K, are:

sale of our common stock by our shareholders, executives, and directors;

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changes in the development status of our product candidates;

any delays or adverse developments or perceived adverse developments with respect to a regulatory agency’s review of our planned pre-clinical and clinical trials;

any delay in our submission for studies or product approvals or adverse regulatory decisions, including failure to receive regulatory approval for our product candidates;

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other events or factors, many of which may be out of our control, including, but not limited to, pandemics such as COVID-19, war, or other acts of God.

In addition, if the market for stocks in our

industry or industries related to our industry, or the stock market in general, experiences a loss of investor confidence, the

trading price of our common stock could decline for reasons unrelated to our business, financial condition and results of operations.

If any of the foregoing occurs, it could cause our stock price to fall and may expose us to lawsuits that, even if unsuccessful,

could be costly to defend and a distraction to management.

In addition, if the market for stocks in our industry

or industries related to our industry, or the stock market in general, experiences a loss of investor confidence, the trading price of

our common stock could decline for reasons unrelated to our business, financial condition and results of operations.

If any of the foregoing

occurs, it could cause our stock price to fall and may expose us to lawsuits that, even if unsuccessful, could be costly to defend and

a distraction to management.

We may acquire other companies or technologies,

which could divert our management’s attention, result in dilution to our shareholders and otherwise disrupt our operations

and adversely affect our operating results.

which could divert our management’s attention, result in dilution to our shareholders and otherwise disrupt our operations and adversely

affect our operating results.

We may in the future seek to acquire or invest

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capabilities or otherwise offer growth opportunities.

The pursuit of potential acquisitions may divert the attention of management

and cause us to incur various expenses in identifying, investigating and pursuing suitable acquisitions, whether or not they are

In addition, we do not have any experience

in acquiring other businesses.

If we acquire additional businesses, we may not be able to integrate the acquired personnel, operations

and technologies successfully, or effectively manage the combined business following the acquisition.

We also may not achieve the

anticipated benefits from the acquired business due to a number of factors, including:

The pursuit of potential acquisitions may divert the attention of management and

cause us to incur various expenses in identifying, investigating and pursuing suitable acquisitions, whether or not they are consummated.

In addition, we do not have any experience in

acquiring other businesses.

If we acquire additional businesses, we may not be able to integrate the acquired personnel, operations and

technologies successfully, or effectively manage the combined business following the acquisition.

We also may not achieve the anticipated

benefits from the acquired business due to a number of factors, including:

inability to integrate or benefit from acquired technologies or services in a profitable manner;

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difficulty converting the customers of the acquired business onto our platform and contract terms, including disparities in the revenue, licensing, support or professional services model of the acquired company;

diversion of management’s attention from other business concerns;

adverse effects to our existing business relationships with business partners and customers as a result of the acquisition;

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at least annually.

In the future, if our acquisitions do not yield expected returns, we may be required to take charges to our

operating results based on this impairment assessment process, which could adversely affect our results of operations.

could also result in dilutive issuances of equity securities or the incurrence of debt, which could adversely affect our operating

In addition, if an acquired business fails to meet our expectations, our operating results, business and financial position

In the future, if our acquisitions do not yield expected returns, we may be required to take charges to our operating

results based on this impairment assessment process, which could adversely affect our results of operations.

Acquisitions could also result

in dilutive issuances of equity securities or the incurrence of debt, which could adversely affect our operating results.

if an acquired business fails to meet our expectations, our operating results, business and financial position may suffer.

Market and economic conditions may negatively

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issues, the U.S.

mortgage market and a declining real estate market, unstable global credit markets and financial conditions, and

volatile oil prices have led to periods of significant economic instability, diminished liquidity and credit availability, declines

in consumer confidence and discretionary spending, diminished expectations for the global economy and expectations of slower global

economic growth going forward, increased unemployment rates, and increased credit defaults in recent years.

Our general business

strategy may be adversely affected by any such economic downturns, volatile business environments and continued unstable or unpredictable

economic and market conditions.

If these conditions continue to deteriorate or do not improve, it may make any necessary debt or

equity financing more difficult to complete, more costly, and more dilutive.

Failure to secure any necessary financing in a timely

manner and on favorable terms could have a material adverse effect on our growth strategy, financial performance, and share price

and could require us to delay or abandon development or commercialization plans.

If securities or industry analysts do

not publish research or reports, or publish unfavorable research or reports about our business, our stock price and trading volume

The trading market for our common stock will

rely in part on the research and reports that industry or financial analysts publish about us, our business, our markets and our

mortgage market and a declining real estate market, unstable global credit markets and financial conditions, and volatile

oil prices have led to periods of significant economic instability, diminished liquidity and credit availability, declines in consumer

confidence and discretionary spending, diminished expectations for the global economy and expectations of slower global economic growth

going forward, increased unemployment rates, and increased credit defaults in recent years.

Our general business strategy may be adversely

affected by any such economic downturns, volatile business environments and continued unstable or unpredictable economic and market conditions.

If these conditions continue to deteriorate or do not improve, it may make any necessary debt or equity financing more difficult to complete,

more costly, and more dilutive.

Failure to secure any necessary financing in a timely manner and on favorable terms could have a material

adverse effect on our growth strategy, financial performance, and share price and could require us to delay or abandon development or

commercialization plans.

If securities or industry analysts do not

publish research or reports, or publish unfavorable research or reports about our business, our stock price and trading volume may decline.

The trading market for our common stock will rely

in part on the research and reports that industry or financial analysts publish about us, our business, our markets and our competitors.

We do not control these analysts.

If securities analysts do not cover our common stock, the lack of research coverage

may adversely affect the market price of our common stock.

Furthermore, if one or more of the analysts who do cover us downgrade

our stock or if those analysts issue other unfavorable commentary about us or our business, our stock price would likely decline.

If one or more of these analysts cease coverage of us or fails to regularly publish reports on us, we could lose visibility in

the market and interest in our stock could decrease, which in turn could cause our stock price or trading volume to decline and

may also impair our ability to expand our business with existing customers and attract new customers.

Because certain of our shareholders

control a significant number of shares of our common stock, they may have effective control over actions requiring shareholder

As of March 11, 2021, our directors, executive

officers, certain of our shareholders and their respective affiliates, beneficially own approximately 39.88% of our outstanding

shares of common stock.

As a result, these shareholders acting together, may have the ability to control the outcome of matters

submitted to our shareholders for approval, including the election of directors and any merger, consolidation or sale of all or

substantially all of our assets.

In addition, these shareholders, acting together, may have the ability to control the management

and affairs of our Company.

Accordingly, this concentration of ownership might harm the market price of our common stock by:

delaying, deferring or preventing a change in corporate control;

impeding a merger, consolidation, takeover or other business combination involving us;

discouraging a potential acquirer from making a tender offer or otherwise attempting to obtain control of us.

If securities analysts do not cover our common stock, the lack of research coverage may adversely affect

the market price of our common stock.

Furthermore, if one or more of the analysts who do cover us downgrade our stock or if those analysts

issue other unfavorable commentary about us or our business, our stock price would likely decline.

If one or more of these analysts cease

coverage of us or fails to regularly publish reports on us, we could lose visibility in the market and interest in our stock could decrease,

which in turn could cause our stock price or trading volume to decline and may also impair our ability to expand our business with existing

customers and attract new customers.

Future sales and issuances of our securities

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We expect that significant additional capital

will be needed in the future to continue our planned operations, including research and development, increased marketing, hiring

new personnel, commercializing our products, and continuing activities as an operating public company.

To the extent we raise additional

capital by issuing equity securities, our shareholders may experience substantial dilution.

We may sell common stock, convertible

securities or other equity securities in one or more transactions at prices and in a manner we determine from time to time.

we sell common stock, convertible securities or other equity securities in more than one transaction, investors may be materially

diluted by subsequent sales.

Such sales may also result in material dilution to our existing shareholders, and new investors could

gain rights superior to our existing shareholders.

will be needed in the future to continue our planned operations, including research and development, increased marketing, hiring new personnel,

commercializing our products, and continuing activities as an operating public company.

To the extent we raise additional capital by issuing

equity securities, our shareholders may experience substantial dilution.

We may sell common stock, convertible securities or other equity

securities in one or more transactions at prices and in a manner we determine from time to time.

If we sell common stock, convertible

securities or other equity securities in more than one transaction, investors may be materially diluted by subsequent sales.

may also result in material dilution to our existing shareholders, and new investors could gain rights superior to our existing shareholders.

We do not intend

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We currently anticipate

that we will retain future earnings for the development, operation and expansion of our business and do not anticipate declaring

or paying any cash dividends for the foreseeable future.

Any return to shareholders will therefore be limited to the increase,

if any, of our share price.

We are an “emerging growth company”

and will be able to avail ourselves of reduced disclosure requirements applicable to emerging growth companies, which could make

our common stock less attractive to investors.

We are an “emerging growth company,”

as defined in the Jumpstart Our Business Startups Act of 2012 (the “JOBS Act”), and we intend to take advantage of

certain exemptions from various reporting requirements that are applicable to other public companies that are not “emerging

growth companies”

including not being required to comply with the auditor attestation requirements of Section 404(b) of the

Sarbanes-Oxley Act of 2002, as amended (“Sarbanes-Oxley”), reduced disclosure obligations regarding executive compensation

in our periodic reports and proxy statements, and exemptions from the requirements of holding a nonbinding advisory vote on executive

compensation and shareholder approval of any golden parachute payments not previously approved.

In addition, pursuant to Section

107 of the JOBS Act, as an “emerging growth company”

we intend to take advantage of the extended transition period

provided in Section 7(a)(2)(B) of the Securities Act, for complying with new or revised accounting standards.

In other words, an

“emerging growth company”

can delay the adoption of certain accounting standards until those standards would otherwise

apply to private companies.

We cannot predict if investors will find our common stock less attractive because we may rely on these

If some investors find our common stock less attractive as a result, there may be a less active trading market for

our common stock and our stock price may be more volatile.

We may take advantage of these reporting exemptions until we are no

longer an “emerging growth company.”

We will remain an “emerging growth company”

until the earliest of

(i) the last day of the fiscal year in which we have total annual gross revenues of $1.07 billion or more;

(ii) the last day of

our fiscal year following the fifth anniversary of the date of our initial public offering;

(iii) the date on which we have issued

more than $1.0 billion in nonconvertible debt during the previous three years;

or (iv) the date on which we are deemed to be a

large accelerated filer under the rules of the SEC.

that we will retain future earnings for the development, operation and expansion of our business and do not anticipate declaring or paying

any cash dividends for the foreseeable future.

Any return to shareholders will therefore be limited to the increase, if any, of our share

We are an “emerging growth company”

and will be able to avail ourselves of reduced disclosure requirements applicable to emerging growth companies, which could make our common

stock less attractive to investors.

We are an “emerging growth company,”

as defined in the Jumpstart Our Business Startups Act of 2012 (the “JOBS Act”), and we intend to take advantage of certain

exemptions from various reporting requirements that are applicable to other public companies that are not “emerging growth companies”

including not being required to comply with the auditor attestation requirements of Section 404(b) of the Sarbanes-Oxley Act of 2002,

as amended (“Sarbanes-Oxley”), reduced disclosure obligations regarding executive compensation in our periodic reports and

proxy statements, and exemptions from the requirements of holding a nonbinding advisory vote on executive compensation and shareholder

approval of any golden parachute payments not previously approved.

In addition, pursuant to Section 107 of the JOBS Act, as an “emerging

growth company” we intend to take advantage of the extended transition period provided in Section 7(a)(2)(B) of the Securities Act,

for complying with new or revised accounting standards.

In other words, an “emerging growth company” can delay the adoption

of certain accounting standards until those standards would otherwise apply to private companies.

We cannot predict if investors will

find our common stock less attractive because we may rely on these exemptions.

If some investors find our common stock less attractive

as a result, there may be a less active trading market for our common stock and our stock price may be more volatile.

We may take advantage

of these reporting exemptions until we are no longer an “emerging growth company.” We will remain an “emerging growth

company” until the earliest of (i) the last day of the fiscal year in which we have total annual gross revenues of $1.07 billion

(ii) the last day of our fiscal year following the fifth anniversary of the date of our initial public offering;

(iii) the date

on which we have issued more than $1.0 billion in nonconvertible debt during the previous three years;

or (iv) the date on which we are

deemed to be a large accelerated filer under the rules of the SEC.

We may be at risk of securities class action litigation.

We may be at risk of securities class action

In the past, biotechnology and pharmaceutical companies have experienced significant stock price volatility, particularly

when associated with binary events such as clinical trials and product approvals.

If we face such litigation, it could result in

substantial costs and a diversion of management’s attention and resources, which could harm our business and results in a

decline in the market price of our common stock.

We are currently listed on The Nasdaq

Capital Market.

If we are unable to maintain listing of our securities on Nasdaq or any stock exchange, our stock price could be

adversely affected and the liquidity of our stock and our ability to obtain financing could be impaired and it may be more difficult

for our shareholders to sell their securities.

Although our common stock is currently listed

on The Nasdaq Capital Market, we may not be able to continue to meet the exchange’s minimum listing requirements or those

of any other national exchange.

If we are unable to maintain listing on Nasdaq or if a liquid market for our common stock does

not develop or is sustained, our common stock may remain thinly traded.

The Listing Rules of Nasdaq require listing

issuers to comply with certain standards in order to remain listed on its exchange.

If, for any reason, we should fail to maintain

compliance with these listing standards and Nasdaq should delist our securities from trading on its exchange and we are unable

to obtain listing on another national securities exchange, a reduction in some or all of the following may occur, each of which

could have a material adverse effect on our shareholders:

the liquidity of our common stock;

the market price of our common stock;

our ability to obtain financing for the continuation of our operations;

the number of investors that will consider investing in our common stock;

the number of market makers in our common stock;

the availability of information concerning the trading prices and volume of our common stock;

the number of broker-dealers willing to execute trades in shares of our common stock.

We may be at risk of securities class action litigation.

In the past, biotechnology and pharmaceutical companies have experienced significant stock price volatility, particularly when associated

with binary events such as clinical trials and product approvals.

If we face such litigation, it could result in substantial costs and

a diversion of management’s attention and resources, which could harm our business and results in a decline in the market price

of our common stock.

If we fail to comply

with the continued listing requirements of The Nasdaq Capital Market, our common stock may be delisted and the price of our common stock

and our ability to access the capital markets could be negatively impacted.

On December 30, 2021, we received

written notice from the Nasdaq Stock Market, LLC (“Nasdaq”) t hat

we were not in compliance with Nasdaq Listing Rule 5550(a)(2), as the minimum bid price of our common stock had been below $1.00

per share for 30 consecutive business days.

In accordance with Nasdaq Listing Rule 5810, we

have a period of 180 calendar days, or until June 28, 2022, to regain compliance with the minimum bid price requirement.

To regain compliance,

the closing bid price of our common stock must meet or exceed $1.00 per share for at least 10 consecutive business days during this 180

calendar day period.

In the event we do not regain compliance by June 28, 2022, we may be eligible for an additional 180 calendar day

grace period if we meet the continued listing standards, with the exception of bid price, for The Nasdaq Capital Market, and we provide

written notice to Nasdaq of our intention to cure the deficiency during the second compliance period.

Although we may effect a reverse

stock split of our issued and outstanding common stock in the future, there can be no assurance that such reverse stock split will enable

us to regain compliance with the Nasdaq minimum bid price requirement.

Financial reporting obligations of being

a public company in the United States are expensive and time-consuming, and our management will be required to devote substantial

time to compliance matters.

a public company in the United States are expensive and time-consuming, and our management will be required to devote substantial time

to compliance matters.

As a publicly traded company we incur significant

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and places significant demands on our management and other personnel, including costs resulting from public company reporting obligations

under the Exchange Act and the rules and regulations regarding corporate governance practices, including those under the Sarbanes-Oxley

Act, the Dodd-Frank Wall Street Reform and Consumer Protection Act, and the listing requirements of The Nasdaq Capital Market.

These rules require the establishment and maintenance of effective disclosure and financial controls and procedures, internal control

over financial reporting and changes in corporate governance practices, among many other complex rules that are often difficult

to implement, monitor and maintain compliance with.

Moreover, despite recent reforms made possible by the JOBS Act, the reporting

requirements, rules, and regulations will make some activities more time-consuming and costly, particularly after we are no longer

an “emerging growth company.”

Our management and other personnel will need to devote a substantial amount of time to

ensure that we comply with all of these requirements and to keep pace with new regulations, otherwise we may fall out of compliance

and risk becoming subject to litigation or being delisted, among other potential problems.

under the Exchange Act and the rules and regulations regarding corporate governance practices, including those under Sarbanes-Oxley, the

Dodd-Frank Wall Street Reform and Consumer Protection Act, and the listing requirements of The Nasdaq Capital Market.

These rules require

the establishment and maintenance of effective disclosure and financial controls and procedures, internal control over financial reporting

and changes in corporate governance practices, among many other complex rules that are often difficult to implement, monitor and maintain

compliance with.

Moreover, despite recent reforms made possible by the JOBS Act, the reporting requirements, rules, and regulations will

make some activities more time-consuming and costly, particularly after we are no longer an “emerging growth company.” Our

management and other personnel will need to devote a substantial amount of time to ensure that we comply with all of these requirements

and to keep pace with new regulations, otherwise we may fall out of compliance and risk becoming subject to litigation or being delisted,

among other potential problems.

If we fail to comply with the rules under

Sarbanes-Oxley related to internal controls and procedures in the future, or, if we discover material weaknesses and other deficiencies

in our internal controls over financial reporting, our stock price could decline significantly and raising capital could be more

in our internal controls over financial reporting, our stock price could decline significantly and raising capital could be more difficult.

Section 404 of Sarbanes-Oxley requires annual

management assessments of the effectiveness of our internal controls over financial reporting.

If we fail to comply with the rules

under Sarbanes-Oxley related to disclosure controls and procedures in the future, or, if we discover material weaknesses and other

deficiencies in our internal controls over financial reporting, our stock price could decline significantly and raising capital

could be more difficult.

If material weaknesses or significant deficiencies are discovered or if we otherwise fail to achieve and

maintain the adequacy of our internal controls, we may not be able to ensure that we can conclude on an ongoing basis that we have

effective internal controls over financial reporting in accordance with Section 404 of Sarbanes-Oxley.

Moreover, effective internal

controls are necessary for us to produce reliable financial reports and are important to helping prevent financial fraud.

cannot provide reliable financial reports or prevent fraud, our business and operating results could be harmed, investors could

lose confidence in our reported financial information, and the trading price of our common stock could drop significantly.

Our Articles of Incorporation,

as amended (“Articles of Incorporation”) our Amended and Restated Bylaws, and Nevada law may have anti-takeover effects

that could discourage, delay or prevent a change in control, which may cause our stock price to decline.

Our Articles of Incorporation, Amended

and Restated Bylaws, and Nevada law could make it more difficult for a third party to acquire us, even if closing such a transaction

would be beneficial to our shareholders.

We are authorized to issue up to 10,000,000 shares of preferred stock, none of which

are outstanding as of March 11, 2021.

This preferred stock may be issued in one or more series, the terms of which may be determined

at the time of issuance by our board of directors without further action by shareholders.

The terms of any series of preferred

stock may include voting rights (including the right to vote as a series on particular matters), preferences as to dividend, liquidation,

conversion and redemption rights and sinking fund provisions.

As of March 11, 2021, 5,000,000 shares of our preferred stock have

been designated as Series A Preferred Stock of which 3,102,480 shares of Series A Preferred Stock which were previously issued

were converted into common stock at the time of our initial public offering and 1,897,520 shares of Series A Preferred Stock remain

The issuance of any preferred stock could materially adversely affect the rights of the holders of our common stock,

and therefore, reduce the value of our common stock.

In particular, specific rights granted to future holders of preferred stock

could be used to restrict our ability to merge with, or sell our assets to, a third party and thereby preserve control by the

present management.

Provisions of our Articles of Incorporation,

our Amended and Restated Bylaws and Nevada law also could have the effect of discouraging potential acquisition proposals or making

a tender offer or delaying or preventing a change in control, including changes a shareholder might consider favorable.

Such provisions

may also prevent or frustrate attempts by our shareholders to replace or remove our management.

In particular, the Articles of

Incorporation, our Amended and Restated Bylaws and Nevada law, as applicable, among other things:

If we fail to comply with the rules under

Sarbanes-Oxley related to disclosure controls and procedures in the future, or, if we discover material weaknesses and other deficiencies

in our internal controls over financial reporting, our stock price could decline significantly and raising capital could be more difficult.

If material weaknesses or significant deficiencies are discovered or if we otherwise fail to achieve and maintain the adequacy of our

internal controls, we may not be able to ensure that we can conclude on an ongoing basis that we have effective internal controls over

financial reporting in accordance with Section 404 of Sarbanes-Oxley.

Moreover, effective internal controls are necessary for us to produce

reliable financial reports and are important to helping prevent financial fraud.

If we cannot provide reliable financial reports or prevent

fraud, our business and operating results could be harmed, investors could lose confidence in our reported financial information, and

the trading price of our common stock could drop significantly.

Our Articles of Incorporation, as amended

(“Articles of Incorporation”), our Amended and Restated Bylaws, and Nevada law may have anti-takeover effects that could discourage,

delay or prevent a change in control, which may cause our stock price to decline.

Our Articles of Incorporation, Amended and Restated

Bylaws, and Nevada law could make it more difficult for a third party to acquire us, even if closing such a transaction would be beneficial

to our shareholders.

We are authorized to issue up to 10,000,000 shares of preferred stock, none of which are outstanding as of March

This preferred stock may be issued in one or more series, the terms of which may be determined at the time of issuance by our

board of directors without further action by shareholders.

The terms of any series of preferred stock may include voting rights (including

the right to vote as a series on particular matters), preferences as to dividend, liquidation, conversion and redemption rights and sinking

fund provisions.

As of March 28, 2022, 5,000,000 shares of our preferred stock have been designated as Series A Preferred Stock of which

3,102,480 shares of Series A Preferred Stock were previously issued and converted into common stock at the time of our initial public

offering and 1,897,520 shares of Series A Preferred Stock remain authorized.

The issuance of any preferred stock could materially adversely

affect the rights of the holders of our common stock, and therefore, reduce the value of our common stock.

In particular, specific rights

granted to future holders of preferred stock could be used to restrict our ability to merge with, or sell our assets to, a third party

and thereby preserve control by the present management.

Provisions of our Articles of Incorporation, our

Amended and Restated Bylaws and Nevada law also could have the effect of discouraging potential acquisition proposals or making a tender

offer or delaying or preventing a change in control, including changes a shareholder might consider favorable.

Such provisions may also

prevent or frustrate attempts by our shareholders to replace or remove our management.

In particular, the Articles of Incorporation, our

Amended and Restated Bylaws and Nevada law, as applicable, among other things:

provide the board of directors with the ability to alter the Amended and Restated Bylaws without shareholder approval;

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Our Amended and Restated Bylaws provide

that the Eighth Judicial District Court of Clark County, Nevada will be the sole and exclusive forum for certain disputes which

could limit shareholders’

ability to obtain a favorable judicial forum for disputes with us or its directors, officers, employees

Our Amended and Restated Bylaws provide that

unless we consent in writing to the selection of an alternative forum, the Eighth Judicial District Court of Clark County, Nevada

shall be the sole and exclusive forum for state law claims with respect to:

(i) any derivative action or proceeding brought in

the name or right of us or on our behalf, (ii) any action asserting a claim for breach of any fiduciary duty owed by any director,

officer, employee or agent to us or our shareholders, (iii) any action arising or asserting a claim arising pursuant to any provision

of Nevada Revised Statutes Chapters 78 or 92A or any provision of our Articles of Incorporation or Amended and Restated Bylaws

or (iv) any action asserting a claim governed by the internal affairs doctrine, including, without limitation, any action to interpret,

apply, enforce or determine the validity of our Articles of Incorporation or Amended and Restated Bylaws.

This exclusive forum

provision would not apply to suits brought to enforce any liability or duty created by the Securities Act or the Exchange Act or

any other claim for which the federal courts have exclusive jurisdiction.

To the extent that any such claims may be based upon

federal law claims, Section 27 of the Exchange Act creates exclusive federal jurisdiction over all suits brought to enforce any

duty or liability created by the Exchange Act or the rules and regulations thereunder.

Furthermore, Section 22 of the Securities

Act creates concurrent jurisdiction for federal and state courts over all suits brought to enforce any duty or liability created

by the Securities Act or the rules and regulations thereunder.

This choice of forum provision may limit a

shareholder’s ability to bring a claim in a judicial forum that it finds favorable for disputes with us or our directors,

officers, other employees or agents, which may discourage such lawsuits against us and our directors, officers, other employees

Alternatively, if a court were to find the choice of forum provision contained in our Amended and Restated Bylaws to

be inapplicable or unenforceable in an action, we may incur additional costs associated with resolving such action in other jurisdictions,

which could have a material adverse effect on our business, results of operations, and financial condition.

that the Eighth Judicial District Court of Clark County, Nevada will be the sole and exclusive forum for certain disputes which could

limit shareholders’ ability to obtain a favorable judicial forum for disputes with us or its directors, officers, employees or agents.

Our Amended and Restated Bylaws provide that unless

we consent in writing to the selection of an alternative forum, the Eighth Judicial District Court of Clark County, Nevada shall be the

sole and exclusive forum for state law claims with respect to:

(i) any derivative action or proceeding brought in the name or right of

us or on our behalf, (ii) any action asserting a claim for breach of any fiduciary duty owed by any director, officer, employee or agent

to us or our shareholders, (iii) any action arising or asserting a claim arising pursuant to any provision of Nevada Revised Statutes

Chapters 78 or 92A or any provision of our Articles of Incorporation or Amended and Restated Bylaws or (iv) any action asserting a claim

governed by the internal affairs doctrine, including, without limitation, any action to interpret, apply, enforce or determine the validity

of our Articles of Incorporation or Amended and Restated Bylaws.

This exclusive forum provision would not apply to suits brought to enforce

any liability or duty created by the Securities Act or the Exchange Act or any other claim for which the federal courts have exclusive

jurisdiction.

To the extent that any such claims may be based upon federal law claims, Section 27 of the Exchange Act creates exclusive

federal jurisdiction over all suits brought to enforce any duty or liability created by the Exchange Act or the rules and regulations

Furthermore, Section 22 of the Securities Act creates concurrent jurisdiction for federal and state courts over all suits

brought to enforce any duty or liability created by the Securities Act or the rules and regulations thereunder.

This choice of forum provision may limit a shareholder’s

ability to bring a claim in a judicial forum that it finds favorable for disputes with us or our directors, officers, other employees

or agents and may result in increased costs to our shareholders, which may discourage such lawsuits against us and our directors,

officers, other employees and agents.

Alternatively, if a court were to find the choice of forum provision contained in our Amended and

Restated Bylaws to be inapplicable or unenforceable in an action, we may incur additional costs associated with resolving such action

in other jurisdictions, which could have a material adverse effect on our business, results of operations, and financial condition.

UNRESOLVED STAFF COMMENTS

Compared sentence by sentence after normalising whitespace, quotation marks, case and digits, so re-formatting and restated figures do not read as changed language. Wording changes appear as one removal and one addition. The current filing and the prior one are authoritative.

What changed 10-K

Item 1A. Risk Factors