What changed in this filing

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Item 1A. Risk Factors

2025-08-05 compared with 2025-05-08 · 83 added, 60 removed, 4 unchanged (97% of the section changed)

In addition to the other information set forth in

this Quarterly Report on Form 10-Q, consider the risk factors discussed in Part 1, “Item 1A.

Risk Factors” in the Company’s

2024 Form 10-K and the risk factors discussed in Item 1A of this Quarterly Report on Form 10-Q, which could materially affect our business,

financial condition or future results.

The risks described in the aforementioned reports are not the only risks facing the Company.

risks and uncertainties not currently known to the Company or that it currently deems to be not material also may materially adversely

affect the Company’s business, financial condition, and/or operating results.

The following are the risk factors that have materially

changed from our risk factors included in our 2024 Form 10-K:

Risks Related to Ownership of Our Common Stock

Our management and directors will be able to exert influence over

As of March 31, 2025, our executive officers and directors

beneficially owned approximately 4.2% of our common stock.

These stockholders, if they act together, may be able to influence our management

and affairs and all matters requiring stockholder approval, including significant corporate transactions.

This concentration of ownership

may have the effect of delaying or preventing a change in control and might affect the market price of our common stock.

The market price of our common stock has been volatile over the past

year and may continue to be volatile.

The market price and trading volume of our common stock

has been volatile over the past year and it may continue to be volatile.

Over the past year, our common stock has traded as low as $3.01

and as high as $10.69 per share.

We cannot predict the price at which our common stock will trade in the future and it may decline.

price at which our common stock trades may fluctuate significantly and may be influenced by many factors, including our financial results;

addition to the other information set forth in this Quarterly Report on Form 10-Q, consider the risk factors discussed in Part 1, “Item

Risk Factors” in the Company’s 2024 Form 10-K, filed with the SEC on March 13, 2025, and the risk factors discussed in Item 1A of the Quarterly Report on Form

10-Q for the quarter ended March 31, 2025, filed with the SEC on May 8, 2025, and in this Quarterly Report on Form 10-Q, which could

materially affect our business, financial condition or future results.

The risks described in the aforementioned reports are not the

only risks facing the Company.

Additional risks and uncertainties not currently known to the Company or that it currently deems to be

not material also may materially adversely affect the Company’s business, financial condition, and/or operating results.

following are the risk factors that have materially changed from our risk factors included in our 2024 Form 10-K:

Related to Our Business and Industry

1154 is in development and an NDA submission may not be filed, or if filed, may not be accepted by the FDA.

1154 is currently in development.

There can be no assurance as to whether the results of the clinical trials in LPCN 1154 for postpartum

depression will support an NDA submission or whether an NDA submission will be accepted for review or approved by the FDA, including

the oral route related brexanolone or its metabolites exposure profile relative to injectable brexanolone.

A safety and efficacy study

in the patient population is ongoing, however there can be no assurance that the safety and efficacy study will be completed, or that

the results from the study will meet the primary endpoint.

Further, there can be no assurance that additional studies will not be required,

and if they are required that we will have sufficient resources to conduct such additional studies to enable an NDA submission.

1154 may not achieve planned commercialization or commercialization objectives for a variety of reasons.

Commercialization

of LPCN 1154 is likely dependent on us finding a partner to market and sell LPCN 1154, if approved.

We are exploring the possibility

of partnering LPCN 1154 to a third party for commercialization, however we may not be able to identify potential partners or successfully

enter into partnership arrangements on terms favorable to us, if at all.

We cannot be certain as to whether label language required by

the FDA will require warnings, blackbox or otherwise, as to the safety or efficacy of LPCN 1154 which could negatively affect the commercialization

of LPCN 1154, if approved.

If we are unable to successfully partner or otherwise develop and get regulatory approval for LPCN 1154,

LPCN 1154 may never be commercialized.

can be no assurance there will not be any third-party patent infringement proceedings against us.

Such proceedings could delay or prevent

further development of LPCN 1154.

addition, we rely on third party vendors for our supply of brexanolone, the active pharmaceutical in LPCN 1154.

If our third party suppliers

are not able to supply brexanolone on a timely basis, or if the cost of obtaining brexanolone increases, our ability to successfully

develop and commercialize LPCN 1154 will be adversely affected.

Related to Ownership of Our Common Stock

management and directors will be able to exert influence over our affairs.

of June 30, 2025, our executive officers and directors beneficially owned approximately 6.5% of our common stock.

These stockholders,

if they act together, may be able to influence our management and affairs and all matters requiring stockholder approval, including significant

corporate transactions.

This concentration of ownership may have the effect of delaying or preventing a change in control and might affect

the market price of our common stock.

market price of our common stock has been volatile over the past year and may continue to be volatile.

market price and trading volume of our common stock has been volatile over the past year and it may continue to be volatile.

past year, our common stock has traded as low as $2.83 and as high as $7.83 per share.

We cannot predict the price at which our common

stock will trade in the future and it may decline.

The price at which our common stock trades may fluctuate significantly and may be

influenced by many factors, including our financial results;

developments generally affecting our industry;

general economic, industry and market conditions, and our customers;

the depth and liquidity

of the market for our common stock;

general economic, industry

and market conditions, and our customers;

the depth and liquidity of the market for our common stock;

investor perceptions of our business;

reports by industry analysts;

announcements by other market

participants, including, among others, investors, our competitors, and our customers;

announcements by other market participants, including, among others, investors, our competitors, and our

regulatory action affecting our business;

impact of other “Risk Factors” discussed herein and in our 2024 Form 10-K.

In addition, changes in the trading price of our

common stock may be inconsistent with our operating results and outlook.

The volatility of the market price of our common stock may be

inconsistent with our operating results and outlook.

The volatility of the market price of our common stock may adversely affect investors’

ability to purchase or sell shares of our common stock.

Risks Relating to Our Financial Position

and Capital Requirements

We have incurred significant operating losses in most years since

our inception and anticipate that we will incur continued losses for the foreseeable future.

We have focused a significant portion of our efforts

on developing TLANDO and more recently on LPCN 1154, LPCN 1148, and LPCN 1144.

We have funded our operations to date through sales of

our equity securities, debt and payments received under our license and collaboration arrangements.

We have incurred losses in most years

since our inception.

As of March 31, 2025, we had an accumulated deficit of $201.6 million.

Substantially all of our operating losses

resulted from costs incurred in connection with our research and development programs and from general and administrative costs associated

with our operations.

These losses, combined with expected future losses, have had and will continue to have an adverse effect on our stockholders’

We expect to continue to incur significant research and development expenses in connection with clinical trials associated with

LPCN 1154, and potentially with LPCN 2401, LPCN 2101, LPCN 2203, LPCN 1148, LPCN 1144 and LPCN 1107, if further clinical trials are initiated.

As a result, we expect to continue to incur significant operating losses for the foreseeable future as we evaluate further clinical development

of LPCN 1154, LPCN 2401, LPCN 2101, LPCN 2203, and possibly LPCN 1148, LPCN 1144, and LPCN 1107, in addition to our other programs and

continued research efforts.

Because of the numerous risks and uncertainties associated with developing pharmaceutical products, we are

unable to predict the extent of any future losses or when we will become profitable, if at all.

and the impact of other “Risk Factors” discussed herein and in our 2024

In addition, changes in the trading price of our common stock may be inconsistent with our operating results and outlook.

The volatility of the market price of our common stock may be inconsistent with our operating results and outlook.

The volatility of

the market price of our common stock may adversely affect investors’ ability to purchase or sell shares of our common stock.

Relating to Our Financial Position and Capital Requirements

have incurred significant operating losses in most years since our inception and anticipate that we will incur continued losses for the

foreseeable future.

have focused a significant portion of our efforts on developing TLANDO and more recently on LPCN 1154, LPCN 1148, and LPCN 1144.

funded our operations to date through sales of our equity securities, debt and payments received under our license and collaboration

arrangements.

We have incurred losses in most years since our inception.

As of June 30, 2025, we had an accumulated deficit of approximately

$203.8 million.

Substantially all of our operating losses resulted from costs incurred in connection with our research and development

programs and from general and administrative costs associated with our operations.

These losses, combined with expected future losses,

have had and will continue to have an adverse effect on our stockholders’ equity.

We expect to continue to incur significant research

and development expenses in connection with clinical trials associated with LPCN 1154 and LPCN 2401, and potentially with LPCN 2101,

LPCN 2203, LPCN 1148, LPCN 1144 and LPCN 1107, if further clinical trials are initiated.

As a result, we expect to continue to incur

significant operating losses for the foreseeable future as we evaluate further clinical development of LPCN 1154, LPCN 2401, LPCN 2101,

LPCN 2203, and possibly LPCN 1148, LPCN 1144, and LPCN 1107, in addition to our other programs and continued research efforts.

of the numerous risks and uncertainties associated with developing pharmaceutical products, we are unable to predict the extent of any

future losses or when we will become profitable, if at all.

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-Q

Item 1A. Risk Factors