Financial Statements
−Removed: NeuroOne Medical Technologies Corporation
−Removed: Condensed Balance Sheets
−Removed: As of December 31,
+Added: Medical Technologies Corporation
+Added: Balance Sheets
+Added: As of March 31,
As of September 30,
17 unchanged sentences
Preferred stock, $ 0.001 par value;
−Removed: 10,000,000 shares authorized as of December 31, 2021 and September 30, 2021;
−Removed: no shares issued or outstanding as of December 31, 2021 and September 30, 2021.
+Added: 10,000,000 shares authorized as of March 31, 2022 and September 30, 2021;
+Added: no shares issued or outstanding as of March 31, 2022 and September 30, 2021.
Common stock, $ 0.001 par value;
−Removed: 100,000,000 shares authorized as of December 31, 2021 and September 30, 2021;
−Removed: 16,187,722 and 12,010,019 shares issued and outstanding as of December 31, 2021 and September 30, 2021, respectively.
+Added: 100,000,000 shares authorized as of March 31, 2022 and September 30, 2021;
+Added: 16,191,169 and 12,010,019 shares issued and outstanding as of March 31, 2022 and September 30, 2021, respectively.
Additional paid–in capital
3 unchanged sentences
Total stockholders’ equity
−Removed: Total liabilities and stockholders’
−Removed: See accompanying notes to
−Removed: condensed financial statements
−Removed: NeuroOne Medical Technologies Corporation
−Removed: Condensed Statements of
−Removed: For the three months ended
+Added: Total liabilities and stockholders’ equity
+Added: accompanying notes to condensed financial statements
+Added: Medical Technologies Corporation
+Added: Statements of Operations
+Added: Three Months Ended
+Added: Six Months Ended
Product revenue
Cost of product revenue
−Removed: Product gross loss
+Added: Product gross profit (loss)
Collaborations revenue
6 unchanged sentences
( 2,395,691 )
+Added: ( 5,869,135 )
+Added: ( 4,539,092 )
Interest expense
3 unchanged sentences
( 2,393,916 )
+Added: ( 5,865,542 )
+Added: ( 4,353,396 )
Provision for income taxes
1 unchanged sentence
$ ( 2,393,916 )
+Added: $ ( 5,865,542 )
+Added: $ ( 4,353,396 )
Net loss per share:
2 unchanged sentences
Basic and diluted
−Removed: See accompanying notes to
−Removed: condensed financial statements
−Removed: NeuroOne Medical Technologies Corporation
−Removed: Condensed Statements of
−Removed: Changes in Stockholders’ Equity
+Added: accompanying notes to condensed financial statements
+Added: Medical Technologies Corporation
+Added: Statements of Changes in Stockholders’ Equity
Stockholders’
9 unchanged sentences
( 32,838,511 )
+Added: Issuance of common stock in connection with private placement
+Added: Issuance of warrants in connection with private placement
+Added: Issuance costs in connection with private placement
+Added: ( 1,198,080 )
+Added: ( 1,198,080 )
+Added: Stock-based compensation
+Added: Exercise of warrants
+Added: Exercise of stock options
+Added: Issuance of common stock upon vesting of restricted stock units
+Added: ( 2,393,916 )
+Added: ( 2,393,916 )
+Added: Balance at March 31, 2021
+Added: $ ( 35,232,427 )
Balance at September 30, 2021
$ ( 40,827,199 )
−Removed: Issuance of common stock in connection with private placement
−Removed: Issuance cost in connection with private placement
+Added: Issuance of common stock in connection with public offering
+Added: Issuance cost in connection with public offering
( 1,352,280 )
6 unchanged sentences
$ ( 43,634,674 )
−Removed: See accompanying notes to
−Removed: condensed financial statements
−Removed: NeuroOne Medical Technologies Corporation
−Removed: Condensed Statements of Cash Flows
−Removed: For the three months ended
+Added: Stock-based compensation
+Added: Issuance of common stock upon vesting of restricted stock units
+Added: ( 3,058,067 )
+Added: ( 3,058,067 )
+Added: Balance at March 31, 2022
+Added: $ ( 46,692,741 )
+Added: accompanying notes to condensed financial statements
+Added: Medical Technologies Corporation
+Added: Statements of Cash Flows
+Added: six months ended
Operating activities
1 unchanged sentence
$ ( 4,353,396 )
−Removed: Adjustments to reconcile net loss to net cash used in operating
+Added: Adjustments to reconcile net loss to net cash used in operating activities:
Amortization and depreciation
7 unchanged sentences
Accounts payable
−Removed: Accrued expenses, deferred revenue, operating leases and other
+Added: Accrued expenses, deferred revenue, operating leases and other liabilities
Net cash used in operating activities
6 unchanged sentences
Issuance costs related to convertible notes
−Removed: Proceeds from issuance of common stock in connection with common
−Removed: stock offering
−Removed: Proceeds from advance related to future financing
−Removed: Issuance costs related to common stock offering
+Added: Proceeds from issuance of common stock in connection with public offering and private placements
+Added: Proceeds from issuance of warrants in connection with private placement
+Added: Exercise of warrants
+Added: Exercise of stock options
+Added: Issuance costs related to public offering and private placements
( 1,327,300 )
+Added: ( 1,190,495 )
Net cash provided by financing activities
2 unchanged sentences
Cash at end of period
−Removed: Supplemental non-cash financing and investing
−Removed: transactions:
+Added: Supplemental non-cash financing and investing transactions:
Conversion of convertible notes into equity
−Removed: Unpaid issuance costs attributed to convertible notes and common
−Removed: stock offering
−Removed: Reclass of deferred offering costs to additional paid-in capital
−Removed: in connection with common stock offering
−Removed: See accompanying notes to
−Removed: condensed financial statements
−Removed: NeuroOne Medical Technologies
−Removed: to Condensed Financial Statements
−Removed: NOTE 1 – Description of Business and
−Removed: Basis of Presentation
−Removed: NeuroOne Medical Technologies Corporation (the
−Removed: “Company” or “NeuroOne”), a Delaware corporation, is an early-stage medical technology company developing comprehensive
−Removed: neuromodulation electroencephalogram (cEEG) and stereoelectrocencephalography (sEEG) recording, monitoring, ablation, and brain stimulation
−Removed: solutions to diagnose and treat patients with epilepsy, Parkinson’s disease, dystonia, essential tremors, chronic pain due to failed
−Removed: back surgeries and other related neurological disorders.
−Removed: The Company received 510(k) clearance from the
−Removed: U.S Food and Drug Administration (“FDA”) for its Evo cortical technology in November 2019, and in September 2021 received
−Removed: 510(k) clearance from the FDA for its Evo sEEG electrode technology for temporary (less than 24 hours) use with recording, monitoring,
−Removed: and stimulation equipment for the recording, monitoring, and stimulation of electrical signals at the subsurface level of the brain.
−Removed: To date, the Company has had limited commercial sales.
−Removed: The Company is based in Eden Prairie, Minnesota.
−Removed: On March 11, 2020, the World Health Organization
−Removed: declared the outbreak of a novel coronavirus (“COVID-19”) as a global pandemic.
−Removed: As a result of the COVID-19 pandemic, the
−Removed: Company has experienced, and will likely continue to experience, delays and disruptions in its pre-clinical and clinical trials, as well
−Removed: as interruptions in its manufacturing, supply chain, shipping, and research and development operations.
−Removed: The development of the Company’s
−Removed: technology was delayed in the first quarter due to interruptions in global manufacturing and shipping as a result of the COVID-19 pandemic.
−Removed: Additionally, the Company’s own staff has been impacted by infections and mandatory quarantines.
−Removed: Testing and clinical trials, manufacturing,
−Removed: component supply, shipping and research and development operations may be further impacted by the continuing effects of COVID-19.
−Removed: The extent to which the COVID-19 pandemic and
−Removed: macroeconomic conditions may further impact the Company’s business will depend on future developments, which are highly uncertain
−Removed: and cannot be predicted with confidence, such as global supply chain disruptions, the duration of the pandemic and the impact of variants,
−Removed: travel restrictions and social distancing in the U.S.
−Removed: and other countries, business closures or business disruptions and the effectiveness
−Removed: of actions taken in the U.S.
+Added: Unpaid issuance costs and non-cash adjustments attributed to convertible notes and private placements
+Added: Reclass of deferred offering costs to additional paid-in capital in connection with public offering
+Added: Purchased fixed assets in accounts payable and accrued expenses
+Added: accompanying notes to condensed financial statements
+Added: NeuroOne Medical Technologies Corporation
+Added: Notes to Condensed Financial Statements
+Added: 1 – Description of Business and Basis of Presentation
+Added: Medical Technologies Corporation (the “Company” or “NeuroOne”), a Delaware corporation, is an early-stage medical
+Added: technology company developing comprehensive neuromodulation electroencephalogram (cEEG) and stereoelectrocencephalography (sEEG) recording,
+Added: monitoring, ablation, and brain stimulation solutions to diagnose and treat patients with epilepsy, Parkinson’s disease, dystonia,
+Added: essential tremors, chronic pain due to failed back surgeries and other related neurological disorders.
+Added: The Company received 510(k) clearance from the U.S.
+Added: Food and Drug Administration (“FDA”) for its Evo cortical technology in November 2019, and in September 2021 received 510(k)
+Added: clearance from the FDA for its Evo sEEG electrode technology for temporary (less than 24 hours) use with recording, monitoring, and stimulation
+Added: equipment for the recording, monitoring, and stimulation of electrical signals at the subsurface level of the brain.
+Added: To date, the Company
+Added: has had limited commercial sales.
+Added: Company is based in Eden Prairie, Minnesota.
+Added: March 11, 2020, the World Health Organization declared the outbreak of a novel coronavirus (“COVID-19”) as a global pandemic.
+Added: As a result of the COVID-19 pandemic, the Company has experienced, and will likely continue to experience, delays and disruptions in
+Added: its pre-clinical and clinical trials, as well as interruptions in its manufacturing, supply chain, shipping, and research and development
+Added: The development of the Company’s technology was delayed in the first quarter due to interruptions in global manufacturing
+Added: and shipping as a result of the COVID-19 pandemic.
+Added: Additionally, the Company’s own staff has been impacted by infections and mandatory
+Added: Testing and clinical trials, manufacturing, component supply, shipping and research and development operations may
+Added: be further impacted by the continuing effects of COVID-19.
+Added: extent to which the COVID-19 pandemic and macroeconomic conditions may further impact the Company’s business will depend on future
+Added: developments, which are highly uncertain and cannot be predicted with confidence, such as global supply chain disruptions, the duration
+Added: of the pandemic and the impact of variants, travel restrictions and social distancing in the U.S.
+Added: and other countries, business closures
+Added: or business disruptions and the effectiveness of actions taken in the U.S.
and other countries to contain and treat the disease.
−Removed: Although the Company cannot estimate the length
−Removed: or gravity of the impact of the COVID-19 outbreak at this time, the continuing impact of the pandemic may have a material adverse effect
−Removed: on the Company’s results of future operations, financial position, and liquidity for the duration of fiscal year 2022 and beyond.
−Removed: Basis of presentation
−Removed: The accompanying unaudited condensed financial
−Removed: statements have been prepared by the Company, pursuant to the rules and regulations of the Securities and Exchange Commission (the “SEC”).
−Removed: Certain information and footnote disclosures normally included in financial statements prepared in accordance with U.S.
−Removed: generally accepted
−Removed: accounting principles (GAAP) have been condensed or omitted pursuant to such rules and regulations.
−Removed: The condensed financial statements
−Removed: may not include all disclosures required by U.S.
−Removed: however, the Company believes that the disclosures are adequate to make the information
−Removed: presented not misleading.
−Removed: These unaudited condensed financial statements should be read in conjunction with the audited financial statements
−Removed: and the notes thereto for the year ended September 30, 2021 included in the Annual Report on Form 10-K.
−Removed: The condensed balance sheet at
−Removed: September 30, 2021 was derived from the audited financial statements of the Company.
−Removed: In the opinion of management, all adjustments,
−Removed: consisting of only normal recurring adjustments that are necessary to present fairly the financial position, results of operations, and
−Removed: cash flows for the interim periods, have been made.
−Removed: The results of operations for the interim periods are not necessarily indicative
−Removed: of the operating results for the full fiscal year or any future periods.
−Removed: NeuroOne Medical Technologies
−Removed: Notes to Condensed Financial
−Removed: Statements, continued
−Removed: NOTE 2 – Going Concern
−Removed: The accompanying condensed financial statements
−Removed: have been prepared on the basis that the Company will continue as a going concern.
−Removed: The Company has incurred losses since inception, negative
−Removed: cash flows from operations, and had an accumulated deficit of $ 43.6 million as of December 31, 2021.
−Removed: The Company has not established
−Removed: a source of revenues to cover its full operating costs, and as such, has been dependent on funding operations through the issuance of
−Removed: debt and sale of equity securities.
−Removed: The Company does not have adequate liquidity to fund its operations without raising additional funds
−Removed: and such actions are not solely within the control of the Company.
−Removed: These factors raise substantial doubt about its ability to continue
−Removed: as a going concern.
−Removed: The financial statements do not include any adjustments that might result from the outcome of this condition.
−Removed: the Company is unable to raise additional funds, or the Company’s anticipated operating results are not achieved, management believes
−Removed: planned expenditures may need to be reduced in order to extend the time period that existing resources can fund the Company’s operations.
−Removed: The Company intends to fund ongoing activities by utilizing its current cash on hand, from product and collaborations revenue and by
−Removed: raising additional capital through equity or debt financings.
−Removed: If management is unable to obtain the necessary capital, it may have a
−Removed: material adverse effect on the operations of the Company and the development of its technology, or the Company may have to cease operations
−Removed: NOTE 3 - Summary of Significant Accounting
−Removed: Reverse Stock Split
−Removed: On March 11, 2021, the Company’s Board
−Removed: of Directors (the “Board”) approved a one-for-three reverse stock split of the Company’s issued and outstanding shares
−Removed: of common stock (the “Reverse Stock Split”) effective end-of-day March 31, 2021.
−Removed: All issued and outstanding common stock and per
−Removed: share amounts contained in the financial statements have been retroactively adjusted to reflect this Reverse Stock Split for all periods
−Removed: In addition, a proportionate adjustment was made to the per share exercise price and the number of shares issuable upon the
−Removed: exercise of all outstanding stock options, restricted stock units and warrants to purchase shares of common stock.
−Removed: A proportionate adjustment
−Removed: was also made to the number of shares reserved for issuance pursuant to the Company’s equity incentive compensation plans to reflect
−Removed: the Reverse Stock Split.
−Removed: Any fraction of a share of common stock that was created as a result of the Reverse Stock Split was rounded
−Removed: up to the next whole share.
−Removed: The authorized shares and par value of the common stock and preferred stock were not adjusted as a result
−Removed: of the Reverse Stock Split.
−Removed: Management’s Use of Estimates
−Removed: The preparation of financial statements in conformity
−Removed: with accounting principles generally accepted in the United States of America requires management to make estimates and assumptions that
−Removed: affect the reported amounts of assets and liabilities, primarily in connection with the convertible promissory notes when outstanding,
−Removed: and disclosure of contingent assets and liabilities at the date of the financial statements and the reported amounts of revenues and
−Removed: expenses during the reporting period.
+Added: the Company cannot estimate the length or gravity of the impact of the COVID-19 outbreak at this time, the continuing impact of the pandemic
+Added: may have a material adverse effect on the Company’s results of future operations, financial position, and liquidity for the duration
+Added: of fiscal year 2022 and beyond.
+Added: of presentation
+Added: accompanying unaudited condensed financial statements have been prepared by the Company, pursuant to the rules and regulations of the
+Added: Securities and Exchange Commission (the “SEC”).
+Added: Certain information and footnote disclosures normally included in financial
+Added: statements prepared in accordance with U.S.
+Added: generally accepted accounting principles (“GAAP”) have been condensed or omitted
+Added: pursuant to such rules and regulations.
+Added: The condensed financial statements may not include all disclosures required by GAAP;
+Added: the Company believes that the disclosures are adequate to make the information presented not misleading.
+Added: These unaudited condensed financial
+Added: statements should be read in conjunction with the audited financial statements and the notes thereto for the year ended September 30,
+Added: 2021 included in the Annual Report on Form 10-K.
+Added: The condensed balance sheet at September 30, 2021 was derived from the audited financial
+Added: statements of the Company.
+Added: the opinion of management, all adjustments, consisting of only normal recurring adjustments that are necessary to present fairly the
+Added: financial position, results of operations, and cash flows for the interim periods, have been made.
+Added: The results of operations for the
+Added: interim periods are not necessarily indicative of the operating results for the full fiscal year or any future periods.
+Added: NeuroOne Medical Technologies Corporation
+Added: Notes to Condensed Financial Statements
+Added: March 11, 2021, the Company’s Board of Directors (the “Board”) approved a one-for-three reverse stock split of the
+Added: Company’s issued and outstanding shares of common stock (the “Reverse Stock Split”) effective end-of-day March 31,
+Added: issued and outstanding common stock and per share amounts contained in the financial statements have been retroactively adjusted to reflect
+Added: this Reverse Stock Split for all periods presented.
+Added: In addition, a proportionate adjustment was made to the per share exercise price
+Added: and the number of shares issuable upon the exercise and/or vesting of all outstanding stock options, restricted stock units and warrants
+Added: to purchase shares of common stock.
+Added: A proportionate adjustment was also made to the number of shares reserved for issuance pursuant to
+Added: the Company’s equity incentive compensation plans to reflect the Reverse Stock Split.
+Added: Any fraction of a share of common stock that
+Added: was created as a result of the Reverse Stock Split was rounded up to the next whole share.
+Added: The authorized shares and par value of the
+Added: common stock and preferred stock were not adjusted as a result of the Reverse Stock Split.
+Added: 2 – Going Concern
+Added: accompanying condensed financial statements have been prepared on the basis that the Company will continue as a going concern.
+Added: has incurred losses since inception, negative cash flows from operations, and had an accumulated deficit of $ 46.7 million as of
+Added: March 31, 2022.
+Added: The Company has not established a source of revenues to cover its full operating costs, and as such, has been dependent
+Added: on funding operations through the issuance of debt and sale of equity securities.
+Added: The Company does not have adequate liquidity to fund
+Added: its operations without raising additional funds and such actions are not solely within the control of the Company.
+Added: These factors raise
+Added: substantial doubt about its ability to continue as a going concern.
+Added: The financial statements do not include any adjustments that might
+Added: result from the outcome of this condition.
+Added: If the Company is unable to raise additional funds, or the Company’s anticipated operating
+Added: results are not achieved, management believes planned expenditures may need to be reduced in order to extend the time period that existing
+Added: resources can fund the Company’s operations.
+Added: The Company intends to fund ongoing activities by utilizing its current cash on hand,
+Added: from product and collaborations revenue and by raising additional capital through equity or debt financings.
+Added: If management is unable
+Added: to obtain the necessary capital, it may have a material adverse effect on the operations of the Company and the development of its technology,
+Added: or the Company may have to cease operations altogether.
+Added: 3 – Summary of Significant Accounting Policies
+Added: Use of Estimates
+Added: preparation of financial statements in conformity with accounting principles generally accepted in the United States of America requires
+Added: management to make estimates and assumptions that affect the reported amounts of assets and liabilities, primarily in connection with
+Added: the convertible promissory notes when outstanding, and disclosure of contingent assets and liabilities at the date of the financial statements
+Added: and the reported amounts of revenues and expenses during the reporting period.
Actual results could differ from those estimates.
−Removed: Revenue Recognition
−Removed: The Company entered into a development and distribution
−Removed: agreement which has current and future revenue recognition implications.
−Removed: See “Note 7 – Zimmer Development Agreement”.
−Removed: Product Revenue
−Removed: Revenues from product sales are recognized when
−Removed: control of the promised goods or services is transferred to the Company’s customers, in an amount that reflects the consideration
−Removed: the Company expects to be entitled to in exchange for those goods or services.
−Removed: At the inception of each contract, performance obligations
−Removed: are identified and the total transaction price is allocated to the performance obligations.
−Removed: The Company commenced commercial sales of
−Removed: cEEG strip/grid and electrode cable assembly products beginning in the first quarter of fiscal year 2021.
−Removed: The Company sold, on a limited
−Removed: application basis for design verification, sEEG depth electrode products for non-human use in late fiscal year 2021 and the first quarter
−Removed: of fiscal year 2022.
−Removed: Cost of Product
−Removed: Cost of product revenue consists of the manufacturing
−Removed: and materials costs incurred by the Company’s third-party contract manufacturer in connection with cEEG strip/grid and sEEG depth
−Removed: electrode products, and outside supplier materials costs in connection with the electrode cable assembly products.
−Removed: In addition, cost
−Removed: of product revenue includes royalty fees incurred in connection with the Company’s license agreements.
−Removed: Collaborations Revenue
−Removed: In determining the appropriate amount of revenue
−Removed: to be recognized as it fulfills its obligations under its agreements, the Company performs the following steps:
−Removed: (i) identification of
−Removed: the promised goods or services in the contract;
−Removed: (ii) determination of whether the promised goods or services are performance obligations
−Removed: including whether they are distinct in the context of the contract;
−Removed: (iii) measurement of the transaction price, including the constraint
−Removed: on variable consideration;
−Removed: (iv) allocation of the transaction price to the performance obligations based on estimated selling prices;
+Added: Company entered into a development and distribution agreement which has current and future revenue recognition implications.
+Added: 7 – Zimmer Development Agreement”.
+Added: from product sales are recognized when control of the promised goods or services is transferred to the Company’s customers, in
+Added: an amount that reflects the consideration the Company expects to be entitled to in exchange for those goods or services.
+Added: At the inception
+Added: of each contract, performance obligations are identified and the total transaction price is allocated to the performance obligations.
+Added: The Company commenced commercial sales of cEEG strip/grid and electrode cable assembly products beginning in the first quarter of fiscal
+Added: The Company sold, on a limited application basis for design verification, sEEG depth electrode products for non-human use
+Added: beginning in late fiscal year 2021.
+Added: NeuroOne Medical Technologies Corporation
+Added: Notes to Condensed Financial Statements
+Added: of Product Revenue
+Added: of product revenue consists of the manufacturing and materials costs incurred by the Company’s third-party contract manufacturer
+Added: in connection with cEEG strip/grid and sEEG depth electrode products, and outside supplier materials costs in connection with the electrode
+Added: cable assembly products.
+Added: In addition, cost of product revenue includes royalty fees incurred in connection with the Company’s license
+Added: Collaborations
+Added: determining the appropriate amount of revenue to be recognized as it fulfills its obligations under its agreements, the Company performs
+Added: the following steps:
+Added: (i) identification of the promised goods or services in the contract;
+Added: (ii) determination of whether the promised
+Added: goods or services are performance obligations including whether they are distinct in the context of the contract;
+Added: (iii) measurement of
+Added: the transaction price, including the constraint on variable consideration;
+Added: (iv) allocation of the transaction price to the performance
+Added: obligations based on estimated selling prices;
and (v) recognition of revenue when (or as) the Company satisfies each performance obligation.
+Added: performance obligation is a promise in a contract to transfer a distinct good or service to the customer and is the unit of account in
+Added: ASC Topic 606.
+Added: Performance obligations may include license rights, development services, and services associated with regulatory submission
+Added: and approval processes.
+Added: Significant management judgment is required to determine the level of effort required under an arrangement and
+Added: the period over which the Company expects to complete its performance obligations under the arrangement.
+Added: If the Company cannot reasonably
+Added: estimate when its performance obligations are either completed or become inconsequential, then revenue recognition is deferred until
+Added: the Company can reasonably make such estimates.
+Added: Revenue is then recognized over the remaining estimated period of performance using the
+Added: cumulative catch-up method.
+Added: part of the accounting for these arrangements, the Company must develop assumptions that require judgment to determine the stand-alone
+Added: selling price of each performance obligation identified in the contract.
+Added: The Company uses key assumptions to determine the stand-alone
+Added: selling price, which may include forecasted revenues, development timelines, reimbursement rates for personnel costs, discount rates
+Added: and probabilities of technical and regulatory success.
+Added: The Company allocates the total transaction price to each performance obligation
+Added: based on the estimated relative standalone selling prices of the promised goods or service underlying each performance obligation.
+Added: of intellectual property :
+Added: If the license to the Company’s intellectual property is determined to be distinct from the other
+Added: performance obligations identified in the arrangement, the Company recognizes revenues from non-refundable, up-front fees allocated to
+Added: the license when the license is transferred to the customer, and the customer can use and benefit from the license.
+Added: For licenses that
+Added: are bundled with other promises, the Company utilizes judgment to assess the nature of the combined performance obligation to determine
+Added: whether the combined performance obligation is satisfied over time or at a point in time and, if over time, the appropriate method of
+Added: measuring progress for purposes of recognizing revenue from non-refundable, up-front fees.
+Added: The Company evaluates the measure of progress
+Added: each reporting period and, if necessary, adjusts the measure of performance and related revenue recognition.
+Added: At the inception of each arrangement that includes milestone payments, the Company evaluates whether the milestones are
+Added: considered probable of being achieved and estimates the amount to be included in the transaction price using the most likely amount method.
+Added: If it is probable that a significant revenue reversal would not occur, the value of the associated milestone (such as a regulatory submission)
+Added: is included in the transaction price.
+Added: Milestone payments that are not within the control of the Company, such as approvals from regulators,
+Added: are not considered probable of being achieved until those approvals are received.
+Added: When the Company’s assessment of probability
+Added: of achievement changes and variable consideration becomes probable, any additional estimated consideration is allocated to each performance
+Added: obligation based on the estimated relative standalone selling prices of the promised goods or service underlying each performance obligation
+Added: and recorded in license, collaboration, and other revenues based upon when the customer obtains control of each element.
NeuroOne Medical Technologies Corporation
−Removed: Notes to Condensed Financial Statements, continued
−Removed: A performance obligation is a promise in a contract
−Removed: to transfer a distinct good or service to the customer and is the unit of account in ASC Topic 606.
−Removed: Performance obligations may include
−Removed: license rights, development services, and services associated with regulatory submission and approval processes.
−Removed: Significant management
−Removed: judgment is required to determine the level of effort required under an arrangement and the period over which the Company expects to
−Removed: complete its performance obligations under the arrangement.
−Removed: If the Company cannot reasonably estimate when its performance obligations
−Removed: are either completed or become inconsequential, then revenue recognition is deferred until the Company can reasonably make such estimates.
−Removed: Revenue is then recognized over the remaining estimated period of performance using the cumulative catch-up method.
−Removed: As part of the accounting for these arrangements,
−Removed: the Company must develop assumptions that require judgment to determine the stand-alone selling price of each performance obligation
−Removed: identified in the contract.
−Removed: The Company uses key assumptions to determine the stand-alone selling price, which may include forecasted
−Removed: revenues, development timelines, reimbursement rates for personnel costs, discount rates and probabilities of technical and regulatory
−Removed: The Company allocates the total transaction price to each performance obligation based on the estimated relative standalone
−Removed: selling prices of the promised goods or service underlying each performance obligation.
−Removed: Licenses of intellectual property :
−Removed: the license to the Company’s intellectual property is determined to be distinct from the other performance obligations identified
−Removed: in the arrangement, the Company recognizes revenues from non-refundable, up-front fees allocated to the license when the license is transferred
−Removed: to the customer, and the customer can use and benefit from the license.
−Removed: For licenses that are bundled with other promises, the Company
−Removed: utilizes judgment to assess the nature of the combined performance obligation to determine whether the combined performance obligation
−Removed: is satisfied over time or at a point in time and, if over time, the appropriate method of measuring progress for purposes of recognizing
−Removed: revenue from non-refundable, up-front fees.
−Removed: The Company evaluates the measure of progress each reporting period and, if necessary, adjusts
−Removed: the measure of performance and related revenue recognition.
−Removed: Milestone payments :
−Removed: At the inception of
−Removed: each arrangement that includes milestone payments, the Company evaluates whether the milestones are considered probable of being achieved
−Removed: and estimates the amount to be included in the transaction price using the most likely amount method.
−Removed: If it is probable that a significant
−Removed: revenue reversal would not occur, the value of the associated milestone (such as a regulatory submission) is included in the transaction
−Removed: Milestone payments that are not within the control of the Company, such as approvals from regulators, are not considered probable
−Removed: of being achieved until those approvals are received.
−Removed: When the Company’s assessment of probability of achievement changes and variable
−Removed: consideration becomes probable, any additional estimated consideration is allocated to each performance obligation based on the estimated
−Removed: relative standalone selling prices of the promised goods or service underlying each performance obligation and recorded in license, collaboration,
−Removed: and other revenues based upon when the customer obtains control of each element.
−Removed: For arrangements that include
−Removed: sales-based royalties, including milestone payments based on the level of sales, and the license is deemed to be the predominant item
−Removed: to which the royalties relate, the Company recognizes revenue at the later of (a) when the related sales occur, or (b) when the performance
−Removed: obligation to which some or all of the royalty has been allocated has been satisfied (or partially satisfied).
−Removed: Fair Value of Financial Instruments
−Removed: The Company’s accounting for fair value
−Removed: measurements of assets and liabilities that are recognized or disclosed at fair value in the financial statements on a recurring or nonrecurring
−Removed: basis adheres to the Financial Accounting Standards Board (“FASB”) fair value hierarchy that prioritizes the inputs to valuation
−Removed: techniques used to measure fair value.
−Removed: The hierarchy gives the highest priority to unadjusted quoted prices in active markets for identical
−Removed: assets or liabilities (Level 1 measurements) and the lowest priority to measurements involving significant unobservable inputs (Level
−Removed: 3 measurements).
+Added: Notes to Condensed Financial Statements
+Added: For arrangements that include sales-based royalties, including milestone payments based on the level of sales, and the license is deemed
+Added: to be the predominant item to which the royalties relate, the Company recognizes revenue at the later of (a) when the related sales occur,
+Added: or (b) when the performance obligation to which some or all of the royalty has been allocated has been satisfied (or partially satisfied).
+Added: Value of Financial Instruments
+Added: Company’s accounting for fair value measurements of assets and liabilities that are recognized or disclosed at fair value in the
+Added: financial statements on a recurring or nonrecurring basis adheres to the Financial Accounting Standards Board (“FASB”) fair
+Added: value hierarchy that prioritizes the inputs to valuation techniques used to measure fair value.
+Added: The hierarchy gives the highest priority
+Added: to unadjusted quoted prices in active markets for identical assets or liabilities (Level 1 measurements) and the lowest priority to measurements
+Added: involving significant unobservable inputs (Level 3 measurements).
The three levels of the fair value hierarchy are as follows:
−Removed: Unadjusted quoted prices in active markets for identical assets or liabilities accessible to the Company at the measurement
Level 1 Inputs:
+Added: quoted prices in active markets for identical assets or liabilities accessible to the Company at the measurement date.
+Added: Level 2 Inputs:
quoted prices included in Level 1 inputs that are observable for the asset or liability, either directly or indirectly, for substantially
3 unchanged sentences
for situations in which there is little, if any, market activity for the asset or liability at the measurement date.
−Removed: As of December 31, 2021 and September 30, 2021,
−Removed: the fair values of cash, accounts receivable, inventory, prepaid expenses, other assets, accounts payable and accrued expenses approximated
−Removed: their carrying values because of the short-term nature of these assets or liabilities.
−Removed: The fair value of the convertible notes while
−Removed: outstanding were based on both the fair value of our common stock, discount associated with the embedded redemption features, and cash
−Removed: flow models discounted at current implied market rates evidenced in recent arms-length transactions representing expected returns by
−Removed: market participants for similar instruments and are based on Level 3 inputs.
−Removed: There were no transfers between fair value hierarchy
−Removed: levels during the three months ended December 31, 2021 and 2020.
−Removed: The following table provides a roll-forward of
−Removed: the convertible notes at fair value on a recurring basis using unobservable level 3 inputs for the three months ended December 31, 2020.
−Removed: There were no convertible notes outstanding during the three months ended December 31, 2021.
−Removed: NeuroOne Medical Technologies Corporation
−Removed: Notes to Condensed Financial Statements, continued
+Added: of March 31, 2022 and September 30, 2021, the fair values of cash, accounts receivable, inventory, prepaid expenses, other assets, accounts
+Added: payable and accrued expenses approximated their carrying values because of the short-term nature of these assets or liabilities.
+Added: fair value of the convertible notes while outstanding were based on both the fair value of our common stock, discount associated with
+Added: the embedded redemption features, and cash flow models discounted at current implied market rates evidenced in recent arms-length transactions
+Added: representing expected returns by market participants for similar instruments and are based on Level 3 inputs.
+Added: were no transfers between fair value hierarchy levels during the six months ended March 31, 2022 and 2021.
+Added: following table provides a roll-forward of the convertible notes at fair value on a recurring basis using unobservable level 3 inputs
+Added: for the six months ended March 31, 2021.
+Added: There were no convertible notes outstanding during the six months ended March 31, 2022.
Convertible notes
3 unchanged sentences
( 1,005,232 )
−Removed: Balance as of end of period – December 31, 2020
−Removed: Intellectual Property
−Removed: The Company has entered into two licensing agreements
−Removed: with major research institutions, which allow for access to certain patented technology and know-how.
−Removed: Payments under those agreements
−Removed: are capitalized and amortized to general and administrative expense over the expected useful life of the acquired technology.
−Removed: Property and Equipment
−Removed: Property and equipment is recorded at cost and
−Removed: reduced by accumulated depreciation.
−Removed: Depreciation expense is recognized over the estimated useful lives of the assets using the straight-line
−Removed: The estimated useful life for equipment and furniture ranges from three to seven years and three years for software.
−Removed: assets acquired for research and development activities and that have alternative use are capitalized over the useful life of the acquired
−Removed: Estimated useful lives are periodically reviewed, and, when appropriate, changes are made prospectively.
−Removed: Software purchased for
−Removed: internal use consists primarily of amounts paid for perpetual licenses to third-party software providers and installation costs.
−Removed: certain events or changes in operating conditions occur, asset lives may be adjusted and an impairment assessment may be performed on
−Removed: the recoverability of the carrying amounts.
−Removed: Maintenance and repairs are charged directly to expense as incurred.
−Removed: Allowances for Doubtful Accounts
−Removed: The Company records a provision for doubtful
−Removed: accounts, when appropriate, based on historical experience and a detailed assessment of the collectability of its accounts receivable.
−Removed: In estimating the allowance for doubtful accounts, the Company considers, among other factors, the aging of the accounts receivable,
−Removed: its historical write-offs, the credit worthiness of each customer, and general economic conditions.
−Removed: Account balances are charged off
−Removed: against the allowance when the Company believes that it is probable that the receivable will not be recovered.
−Removed: Actual write-offs may
−Removed: be in excess of the Company’s estimated allowance.
−Removed: Inventories are stated at the lower of cost (using
−Removed: the first-in, first-out “FIFO” method) or net realizable value.
−Removed: The Company calculates inventory valuation adjustments for
−Removed: excess and obsolete inventory, when appropriate, based on current inventory levels, movement, expected useful lives, and estimated future
−Removed: demand of the products and spare parts.
−Removed: The Company’s inventory is currently comprised of cEEG strip/grid, sEEG depth electrode
−Removed: and electrode cable assembly finished good products and related component parts.
−Removed: The strip/ grid and depth electrode products are produced
−Removed: by a third-party contract manufacturer and the electrode cable assembly products are obtained from outside suppliers.
−Removed: Impairment of Long-Lived Assets
−Removed: The Company evaluates its long-lived assets,
−Removed: which consist of licensed intellectual property and property and equipment for impairment whenever events or changes in circumstances
−Removed: indicate that the carrying value of these assets may not be recoverable.
−Removed: The Company assesses the recoverability of long-lived assets
−Removed: by determining whether or not the carrying value of such assets will be recovered through undiscounted expected future cash flows.
−Removed: the asset is considered to be impaired, the amount of any impairment is measured as the difference between the carrying value and the
−Removed: fair value of the impaired asset.
−Removed: Research and Development Costs
−Removed: Research and development costs are charged to
−Removed: expense as incurred.
−Removed: Research and development expenses may include costs incurred in performing research and development activities,
−Removed: including clinical trial costs, manufacturing costs for both clinical and pre-clinical materials as well as other contracted services,
−Removed: license fees, and other external costs.
−Removed: Non-refundable advance payments for goods and services that will be used in future research and
−Removed: development activities are expensed when the activity is performed or when the goods have been received, rather than when payment is
−Removed: made, in accordance with Accounting Standards Codification (ASC) 730, Research and Development .
−Removed: Selling, General and Administrative
−Removed: Selling, general and administrative expenses
−Removed: consist primarily of personnel-related costs including stock-based compensation for personnel in functions not directly associated with
−Removed: research and development activities.
−Removed: Other significant costs include legal fees relating to corporate matters, intellectual property
−Removed: costs, professional fees for consultants assisting with regulatory, clinical, product development, financial matters and sales and marketing
−Removed: in connection with the commercial sale of cEEG strip/grid, sEEG depth electrode and electrode cable assembly products.
+Added: Balance as of end of period – March 31, 2021
+Added: Company has entered into two licensing agreements with major research institutions, which allow for access to certain patented technology
+Added: and know-how.
+Added: Payments under those agreements are capitalized and amortized to general and administrative expense over the expected useful
+Added: life of the acquired technology.
NeuroOne Medical Technologies Corporation
−Removed: Notes to Condensed Financial Statements, continued
−Removed: For the Company, income taxes are accounted for
−Removed: under the asset and liability method.
−Removed: Deferred tax assets and liabilities are recognized for the future tax consequences attributable
−Removed: to differences between the financial statement carrying amounts of existing assets and liabilities and their respective tax base and
−Removed: operating loss and tax credit carryforwards.
−Removed: Deferred tax assets and liabilities are measured using enacted tax rates expected to apply
−Removed: to taxable income in the years in which those temporary differences are expected to be recovered or settled.
−Removed: Deferred tax assets are
−Removed: reduced by a valuation allowance if it is more likely than not that some portion or all of the deferred tax asset will not be realized.
−Removed: Net Loss Per Share
−Removed: For the Company, basic loss per share of common
−Removed: stock is computed by dividing net loss by the weighted average number of shares of common stock outstanding during the period.
−Removed: Diluted earnings or loss per share of common
−Removed: stock is computed similarly to basic earnings or loss per share except the weighted average shares outstanding are increased to include
−Removed: additional shares from the assumed exercise of any common stock equivalents, if dilutive.
−Removed: The Company’s warrants, stock options
−Removed: and restricted stock units while outstanding are considered common stock equivalents for this purpose.
−Removed: Diluted earnings is computed utilizing
−Removed: the treasury method for the warrants, stock options and restricted stock units.
−Removed: No incremental common stock equivalents were included
−Removed: in calculating diluted loss per share because such inclusion would be anti-dilutive given the net loss reported for the three months
−Removed: ended December 31, 2021 and 2020.
−Removed: The following potential common shares were not
−Removed: considered in the computation of diluted net loss per share as their effect would have been anti-dilutive for the three months ended
−Removed: December 31, 2021 and 2020:
+Added: Notes to Condensed Financial Statements
+Added: and Equipment
+Added: and equipment is recorded at cost and reduced by accumulated depreciation.
+Added: Depreciation expense is recognized over the estimated useful
+Added: lives of the assets using the straight-line method.
+Added: The estimated useful life for equipment and furniture ranges from three to seven
+Added: years and three years for software.
+Added: Tangible assets acquired for research and development activities and that have alternative use are
+Added: capitalized over the useful life of the acquired asset.
+Added: Estimated useful lives are periodically reviewed, and, when appropriate, changes
+Added: are made prospectively.
+Added: Software purchased for internal use consists primarily of amounts paid for perpetual licenses to third-party
+Added: software providers and installation costs.
+Added: When certain events or changes in operating conditions occur, asset lives may be adjusted
+Added: and an impairment assessment may be performed on the recoverability of the carrying amounts.
+Added: Maintenance and repairs are charged directly
+Added: to expense as incurred.
+Added: for Doubtful Accounts
+Added: Company records a provision for doubtful accounts, when appropriate, based on historical experience and a detailed assessment of the
+Added: collectability of its accounts receivable.
+Added: In estimating the allowance for doubtful accounts, the Company considers, among other factors,
+Added: the aging of the accounts receivable, its historical write-offs, the credit worthiness of each customer, and general economic conditions.
+Added: Account balances are charged off against the allowance when the Company believes that it is probable that the receivable will not be
+Added: Actual write-offs may be in excess of the Company’s estimated allowance.
+Added: are stated at the lower of cost (using the first-in, first-out “FIFO” method) or net realizable value.
+Added: The Company calculates
+Added: inventory valuation adjustments for excess and obsolete inventory, when appropriate, based on current inventory levels, movement, expected
+Added: useful lives, and estimated future demand of the products and spare parts.
+Added: The Company’s inventory is currently comprised of cEEG
+Added: strip/grid, sEEG depth electrode and electrode cable assembly finished good products and related component parts.
+Added: The strip/ grid and
+Added: depth electrode products are produced by a third-party contract manufacturer and the electrode cable assembly products are obtained from
+Added: outside suppliers.
+Added: of Long-Lived Assets
+Added: Company evaluates its long-lived assets, which consist of licensed intellectual property and property and equipment for impairment whenever
+Added: events or changes in circumstances indicate that the carrying value of these assets may not be recoverable.
+Added: The Company assesses the
+Added: recoverability of long-lived assets by determining whether or not the carrying value of such assets will be recovered through undiscounted
+Added: expected future cash flows.
+Added: If the asset is considered to be impaired, the amount of any impairment is measured as the difference between
+Added: the carrying value and the fair value of the impaired asset.
+Added: and Development Costs
+Added: and development costs are charged to expense as incurred.
+Added: Research and development expenses may include costs incurred in performing
+Added: research and development activities, including clinical trial costs, manufacturing costs for both clinical and pre-clinical materials
+Added: as well as other contracted services, license fees, and other external costs.
+Added: Non-refundable advance payments for goods and services
+Added: that will be used in future research and development activities are expensed when the activity is performed or when the goods have been
+Added: received, rather than when payment is made, in accordance with Accounting Standards Codification (ASC) 730, Research and Development .
+Added: General and Administrative
+Added: general and administrative expenses consist primarily of personnel-related costs including stock-based compensation for personnel in
+Added: functions not directly associated with research and development activities.
+Added: Other significant costs include legal fees relating to corporate
+Added: matters, intellectual property costs, professional fees for consultants assisting with regulatory, clinical, product development, financial
+Added: matters and sales and marketing in connection with the commercial sale of cEEG strip/grid, sEEG depth electrode and electrode cable assembly
+Added: NeuroOne Medical Technologies Corporation
+Added: Notes to Condensed Financial Statements
+Added: the Company, income taxes are accounted for under the asset and liability method.
+Added: Deferred tax assets and liabilities are recognized
+Added: for the future tax consequences attributable to differences between the financial statement carrying amounts of existing assets and liabilities
+Added: and their respective tax base and operating loss and tax credit carryforwards.
+Added: Deferred tax assets and liabilities are measured using
+Added: enacted tax rates expected to apply to taxable income in the years in which those temporary differences are expected to be recovered
+Added: Deferred tax assets are reduced by a valuation allowance if it is more likely than not that some portion or all of the deferred
+Added: tax asset will not be realized.
+Added: Loss Per Share
+Added: the Company, basic loss per share of common stock is computed by dividing net loss by the weighted average number of shares of common
+Added: stock outstanding during the period.
+Added: earnings or loss per share of common stock is computed similarly to basic earnings or loss per share except the weighted average shares
+Added: outstanding are increased to include additional shares from the assumed exercise of any common stock equivalents, if dilutive.
+Added: The Company’s
+Added: warrants, stock options, and restricted stock units while outstanding are considered common stock equivalents for this purpose.
+Added: earnings is computed utilizing the treasury method for the warrants, stock options and restricted stock units.
+Added: No incremental common
+Added: stock equivalents were included in calculating diluted loss per share because such inclusion would be anti-dilutive given the net loss
+Added: reported for the three and six months ended March 31, 2022 and 2021.
+Added: following potential common shares were not considered in the computation of diluted net loss per share as their effect would have been
+Added: anti-dilutive for the three and six months ended March 31, 2022 and 2021:
Stock options
−Removed: Restricted stock units and awards
−Removed: Recent Accounting Pronouncements
−Removed: In June 2016, the FASB issued Accounting Standards
−Removed: Update (“ASU”) 2016-13, “ Financial Instruments – Credit Losses” .
−Removed: The ASU sets forth a “current
−Removed: expected credit loss” (“CECL”) model which requires the Company to measure all expected credit losses for financial
−Removed: instruments held at the reporting date based on historical experience, current conditions, and reasonable supportable forecasts.
−Removed: replaces the existing incurred loss model and is applicable to the measurement of credit losses on financial assets measured at amortized
−Removed: cost and applies to some off-balance sheet credit exposures.
−Removed: This ASU is effective for fiscal years beginning after December 15, 2019,
−Removed: including interim periods within those fiscal years, with early adoption permitted.
−Removed: Recently, the FASB issued the final ASU to delay
−Removed: adoption for smaller reporting companies to calendar year 2023.
−Removed: The Company is currently assessing the impact of the adoption of this
−Removed: ASU on its financial statements.
−Removed: In December 2019, the FASB issued ASU No.
−Removed: Income Taxes (Topic 740) which amends the existing guidance relating to the accounting for income taxes.
−Removed: This ASU is intended to simplify
−Removed: the accounting for income taxes by removing certain exceptions to the general principles of accounting for income taxes and to improve
−Removed: the consistent application of GAAP for other areas of accounting for income taxes by clarifying and amending existing guidance.
−Removed: is effective for fiscal years beginning after December 15, 2020.
−Removed: The Company adopted the new guidance on October 1, 2021 and the adoption
−Removed: of this new guidance did not have a material impact on the Company’s financial statements.
−Removed: In August 2020, FASB issued ASU 2020-06, Debt—Debt
−Removed: with Conversion and Other Options (Subtopic 470-20) and Derivatives and Hedging—Contracts in Entity’s Own Equity (Subtopic
−Removed: Accounting for Convertible Instruments and Contracts in an Entity’s Own Equity, which, among other things, provides guidance
−Removed: on how to account for contracts on an entity’s own equity.
−Removed: This ASU eliminates the beneficial conversion and cash conversion accounting
−Removed: models for convertible instruments.
−Removed: It also amends the accounting for certain contracts in an entity’s own equity that are currently
−Removed: accounted for as derivatives because of specific settlement provisions.
−Removed: In addition, this ASU modifies how particular convertible instruments
−Removed: and certain contracts that may be settled in cash or shares impact the diluted EPS computation.
−Removed: The amendments in this ASU are effective
−Removed: for smaller reporting companies as defined by the SEC for fiscal years beginning after December 15, 2023, including interim periods within
−Removed: those fiscal years.
−Removed: Early adoption is permitted, but no earlier than fiscal years beginning after December 15, 2020.
−Removed: The Company is currently
−Removed: evaluating the impact of ASU 2020-06 on its financial statements.
−Removed: NOTE 4 - Commitments and Contingencies
−Removed: WARF License Agreement
−Removed: The Company has entered into an exclusive start-up
−Removed: company license agreement with the Wisconsin Alumni Research Foundation (“WARF”) for WARF’s neural probe array and
−Removed: thin film micro electrode technology (the “WARF Agreement”).
−Removed: The Company entered into an Amended and Restated Exclusive Start-up
−Removed: Company License Agreement (the “WARF License”) with WARF on January 21, 2020, which amended and restated in full the prior
−Removed: license agreement between WARF and NeuroOne, LLC, a predecessor of the Company, dated October 1, 2014, as amended on February 22, 2017,
−Removed: March 30, 2019 and September 18, 2019.
+Added: Restricted stock units
+Added: Accounting Pronouncements
+Added: June 2016, the FASB issued Accounting Standards Update (“ASU”) 2016-13, “ Financial Instruments – Credit Losses” .
+Added: The ASU sets forth a “current expected credit loss” (“CECL”) model which requires the Company to measure all
+Added: expected credit losses for financial instruments held at the reporting date based on historical experience, current conditions, and reasonable
+Added: supportable forecasts.
+Added: This replaces the existing incurred loss model and is applicable to the measurement of credit losses on financial
+Added: assets measured at amortized cost and applies to some off-balance sheet credit exposures.
+Added: This ASU is effective for fiscal years beginning
+Added: after December 15, 2019, including interim periods within those fiscal years, with early adoption permitted.
+Added: Recently, the FASB issued
+Added: the final ASU to delay adoption for smaller reporting companies to calendar year 2023.
+Added: The Company is currently assessing the impact
+Added: of the adoption of this ASU on its financial statements.
+Added: December 2019, the FASB issued ASU No.
+Added: 2019-12, Income Taxes (Topic 740) which amends the existing guidance relating to the accounting
+Added: for income taxes.
+Added: This ASU is intended to simplify the accounting for income taxes by removing certain exceptions to the general principles
+Added: of accounting for income taxes and to improve the consistent application of GAAP for other areas of accounting for income taxes by clarifying
+Added: and amending existing guidance.
+Added: The ASU is effective for fiscal years beginning after December 15, 2020.
+Added: The Company adopted the new
+Added: guidance on October 1, 2021 and the adoption of this new guidance did not have a material impact on the Company’s financial statements.
NeuroOne Medical Technologies Corporation
−Removed: Notes to Condensed Financial Statements, continued
−Removed: The WARF License grants to the Company an exclusive
−Removed: license to make, use and sell, in the United States only, products that employ certain licensed patents for a neural probe array
−Removed: or thin-film micro electrode array and method.
−Removed: We have agreed to pay WARF a royalty equal to a single-digit percentage of our product
−Removed: sales pursuant to the WARF License, with a minimum annual royalty payment of $ 50,000 for 2020, $ 100,000 for 2021 and $ 150,000 for
−Removed: 2022 and each calendar year thereafter that the WARF License is in effect.
−Removed: If we or any of our sublicensees contest the validity of any
−Removed: licensed patent, the royalty rate will be doubled during the pendency of such contest and, if the contested patent is found to be valid
−Removed: and would be infringed by us if not for the WARF License, the royalty rate will be tripled for the remaining term of the WARF License.
−Removed: WARF may terminate the WARF License on 30 days’
−Removed: written notice if we default on the payments of amounts due to WARF or fail to timely submit development reports, actively pursue our
−Removed: development plan or breach any other covenant in the WARF License and fail to remedy such default in 90 days or in the event of certain
−Removed: bankruptcy events involving us.
−Removed: WARF may also terminate the WARF License (i) on 90 days’ notice if we had failed to have commercial
−Removed: sales of one or more FDA-approved products under the WARF License by June 30, 2021 or (ii) if, after royalties earned on sales begin
−Removed: to be paid, such earned royalties cease for more than four calendar quarters.
−Removed: The first commercial sale occurred on December 7, 2020,
−Removed: prior to the June 30, 2021 deadline.
−Removed: The WARF License otherwise expires by its terms on the date that no valid claims on the patents
−Removed: licensed thereunder remain.
−Removed: We expect the latest expiration of a licensed patent to occur in 2030.
−Removed: During the three months ended December
−Removed: 31, 2021 and 2020, $ 25,000 and $ 50,000 in royalty fees were incurred related to the WARF License, respectively, and were reflected as
−Removed: a component of cost of product revenue.
−Removed: Mayo Agreement
−Removed: The Company has an exclusive license and development
−Removed: agreement with the Mayo Foundation for Medical Education and Research (“Mayo”) related to certain intellectual property and
−Removed: development services for thin film micro electrode technology (“Mayo Agreement”).
−Removed: If the Company is successful in obtaining
−Removed: regulatory approval, the Company is to pay royalties to Mayo based on a percentage of net sales of products of the licensed technology
−Removed: through the term of the Mayo Agreement, set to expire May 25, 2037.
−Removed: During the three months ended December 31, 2021 and 2020, $ 739
−Removed: and $ 2,144 in royalty fees were incurred related to the Mayo Agreement, respectively, and were reflected as a component of cost of product
−Removed: PMT Litigation
−Removed: From time to time, the Company is subject to
−Removed: litigation and claims in the ordinary course of business.
−Removed: On March 29, 2018, the Company was served with
−Removed: a complaint filed by PMT Corporation (“PMT”), the former employer of Mark Christianson, a current Company employee, and Wade
−Removed: Fredrickson, a now former Company employee.
+Added: Notes to Condensed Financial Statements
+Added: August 2020, FASB issued ASU 2020-06, Debt—Debt with Conversion and Other Options (Subtopic 470-20) and Derivatives and Hedging—Contracts
+Added: in Entity’s Own Equity (Subtopic 815-40):
+Added: Accounting for Convertible Instruments and Contracts in an Entity’s Own Equity,
+Added: which, among other things, provides guidance on how to account for contracts on an entity’s own equity.
+Added: This ASU eliminates the
+Added: beneficial conversion and cash conversion accounting models for convertible instruments.
+Added: It also amends the accounting for certain contracts
+Added: in an entity’s own equity that are currently accounted for as derivatives because of specific settlement provisions.
+Added: this ASU modifies how particular convertible instruments and certain contracts that may be settled in cash or shares impact the diluted
+Added: EPS computation.
+Added: The amendments in this ASU are effective for smaller reporting companies as defined by the SEC for fiscal years beginning
+Added: after December 15, 2023, including interim periods within those fiscal years.
+Added: Early adoption is permitted, but no earlier than fiscal
+Added: years beginning after December 15, 2020.
+Added: The Company is currently evaluating the impact of ASU 2020-06 on its financial statements.
+Added: In November 2021, the FASB issued ASU 2021-10, Government
+Added: Assistance (Topic 832) - Disclosures by Business Entities about Government Assistance, to increase the transparency of government
+Added: assistance including the disclosure of the types of assistance, an entity’s accounting for the assistance, and the effect of the
+Added: assistance on an entity’s financial statements.
+Added: The amendments in this ASU are effective for all entities within their scope for
+Added: financial statements issued for annual periods beginning after December 15, 2021.
+Added: The Company does not expect that this guidance will
+Added: have a material impact to our financial statements.
+Added: 4 - Commitments and Contingencies
+Added: License Agreement
+Added: Company has entered into an exclusive start-up company license agreement with the Wisconsin Alumni Research Foundation (“WARF”)
+Added: for WARF’s neural probe array and thin film micro electrode technology (the “WARF Agreement”).
+Added: The Company entered
+Added: into an Amended and Restated Exclusive Start-up Company License Agreement (the “WARF License”) with WARF on January 21, 2020,
+Added: which amended and restated in full the prior license agreement between WARF and NeuroOne, LLC, a predecessor of the Company, dated October
+Added: 1, 2014, as amended on February 22, 2017, March 30, 2019 and September 18, 2019.
+Added: WARF License grants to the Company an exclusive license to make, use and sell, in the United States only, products that employ certain
+Added: licensed patents for a neural probe array or thin-film micro electrode array and method.
+Added: We have agreed to pay WARF a royalty equal to
+Added: a single-digit percentage of our product sales pursuant to the WARF License, with a minimum annual royalty payment of $ 50,000 for
+Added: 2020, $ 100,000 for 2021 and $ 150,000 for 2022 and each calendar year thereafter that the WARF License is in effect.
+Added: any of our sublicensees contest the validity of any licensed patent, the royalty rate will be doubled during the pendency of such contest
+Added: and, if the contested patent is found to be valid and would be infringed by us if not for the WARF License, the royalty rate will be
+Added: tripled for the remaining term of the WARF License.
+Added: may terminate the WARF License on 30 days’ written notice if we default on the payments of amounts due to WARF or fail to timely
+Added: submit development reports, actively pursue our development plan or breach any other covenant in the WARF License and fail to remedy
+Added: such default in 90 days or in the event of certain bankruptcy events involving us.
+Added: WARF may also terminate the WARF License (i) on 90
+Added: days’ notice if we had failed to have commercial sales of one or more FDA-approved products under the WARF License by June 30,
+Added: 2021 or (ii) if, after royalties earned on sales begin to be paid, such earned royalties cease for more than four calendar quarters.
+Added: The first commercial sale occurred on December 7, 2020, prior to the June 30, 2021 deadline.
+Added: The WARF License otherwise expires
+Added: by its terms on the date that no valid claims on the patents licensed thereunder remain.
+Added: We expect the latest expiration of a licensed
+Added: patent to occur in 2030.
+Added: During the three months ended March 31, 2022 and 2021, $ 37,500 and $ 25,000 in royalty fees were incurred related
+Added: to the WARF License, respectively.
+Added: During the six months ended March 31, 2022 and 2021, $ 62,500 and $ 75,000 in royalty fees were incurred
+Added: related to the WARF License, respectively.
+Added: The royalty fees were reflected as a component of cost of product revenue.
+Added: NeuroOne Medical Technologies Corporation
+Added: Notes to Condensed Financial Statements
+Added: Company has an exclusive license and development agreement with the Mayo Foundation for Medical Education and Research (“Mayo”)
+Added: related to certain intellectual property and development services for thin film micro electrode technology (“Mayo Agreement”).
+Added: If the Company is successful in obtaining regulatory approval, the Company is to pay royalties to Mayo based on a percentage of net sales
+Added: of products of the licensed technology through the term of the Mayo Agreement, set to expire May 25, 2037.
+Added: During the three months
+Added: ended March 31, 2022 and 2021, $ 1,097 and $ 547 in royalty fees were incurred related to the Mayo Agreement, respectively.
+Added: six months ended March 31, 2022 and 2021, $ 1,836 and $ 2,691 in royalty fees were incurred related to the Mayo Agreement, respectively.
+Added: The royalty fees were reflected as a component of cost of product revenue.
+Added: time to time, the Company is subject to litigation and claims in the ordinary course of business.
+Added: March 29, 2018, the Company was served with a complaint filed by PMT Corporation (“PMT”), the former employer of Mark Christianson,
+Added: a current Company employee, and Wade Fredrickson, a now former Company employee.
The complaint added the Company, NeuroOne, Inc.
−Removed: Christianson to its existing lawsuit
+Added: Christianson to its existing lawsuit against Mr.
Fredrickson in the Fourth Judicial District Court of the State of Minnesota.
−Removed: In the lawsuit, PMT claims that Mr.
−Removed: Christianson, by virtue of their work for the Company and their prior work during employment with PMT, breached their non-competition,
−Removed: non-solicitation and non-disclosure obligations, breached their fiduciary duty obligations, were unjustly enriched, engaged in unfair
−Removed: competition, engaged in a civil conspiracy, tortiously interfered with PMT’s contracts and prospective economic advantage, and
−Removed: breached a covenant of good faith and fair dealing.
+Added: the lawsuit, PMT claims that Mr.
+Added: Fredrickson and Mr.
+Added: Christianson, by virtue of their work for the Company and their prior work during
+Added: employment with PMT, breached their non-competition, non-solicitation and non-disclosure obligations, breached their fiduciary duty obligations,
+Added: were unjustly enriched, engaged in unfair competition, engaged in a civil conspiracy, tortiously interfered with PMT’s contracts
+Added: and prospective economic advantage, and breached a covenant of good faith and fair dealing.
The complaint purported to attach Mr.
−Removed: Fredrickson’s noncompete agreement as
−Removed: Fredrickson, PMT also alleged that he intentionally or negligently spoliated evidence, made negligent or fraudulent
−Removed: misrepresentations, misappropriated trade secrets in violation of Minnesota law, and committed the tort of conversion and statutory civil
+Added: Fredrickson’s
+Added: noncompete agreement as Exhibit A.
+Added: Fredrickson, PMT also alleged that he intentionally or negligently spoliated evidence,
+Added: made negligent or fraudulent misrepresentations, misappropriated trade secrets in violation of Minnesota law, and committed the tort
+Added: of conversion and statutory civil theft.
Against the Company and NeuroOne, Inc., PMT alleged that the Company and NeuroOne, Inc.
−Removed: were unjustly enriched and engaged in
−Removed: unfair competition.
+Added: unjustly enriched and engaged in unfair competition.
PMT asked the Court to impose a constructive trust over the shares held by Mr.
−Removed: Fredrickson and Mr.
−Removed: Christianson and
−Removed: to award compensatory damages, equitable relief, punitive damages, attorneys’ fees, costs and interest.
−Removed: On April 18, 2018, Mr.
−Removed: Christianson, the Company
−Removed: and NeuroOne, Inc.
+Added: Christianson and to award compensatory damages, equitable relief, punitive damages, attorneys’ fees, costs and interest.
+Added: April 18, 2018, Mr.
+Added: Christianson, the Company and NeuroOne, Inc.
filed a motion for dismissal, which was heard by the Court on October
1 unchanged sentence
the contract claims against Mr.
−Removed: Christianson fail because his agreement was not supported by consideration;
−Removed: the Minnesota Uniform Trade
−Removed: Secrets Act preempts plaintiff’s claims for unfair competition, civil conspiracy and unjust enrichment;
−Removed: plaintiff fails to state
−Removed: a claim regarding alleged breach of the duties of loyalty and good faith/fair dealing;
−Removed: plaintiff cannot legally obtain a constructive
+Added: Christianson fail because his agreement was not supported
+Added: by consideration;
+Added: the Minnesota Uniform Trade Secrets Act preempts plaintiff’s claims for unfair competition, civil conspiracy
+Added: and unjust enrichment;
+Added: plaintiff fails to state a claim regarding alleged breach of the duties of loyalty and good faith/fair dealing;
+Added: plaintiff cannot legally obtain a constructive trust;
plaintiff has insufficiently pled its tortious interference claims;
−Removed: and Plaintiff has not stated a claim for unfair competition.
−Removed: On January 7, 2019, the judge granted the motion for dismissal with respect to PMT’s claim for breach of the duty of good faith
−Removed: and fair dealing, and denied the motion for dismissal with respect to the other claims presented.
−Removed: In April 2019, PMT served the Company, NeuroOne,
−Removed: and Christianson with a proposed Second Amended Complaint, which included new claims against the Company and NeuroOne, Inc for tortious
−Removed: interference with contract and tortious interference with prospective business advantage and punitive damages against the Company, NeuroOne
+Added: and Plaintiff
+Added: has not stated a claim for unfair competition.
+Added: On January 7, 2019, the judge granted the motion for dismissal with respect to PMT’s
+Added: claim for breach of the duty of good faith and fair dealing, and denied the motion for dismissal with respect to the other claims presented.
+Added: April 2019, PMT served the Company, NeuroOne, Inc.
+Added: and Christianson with a proposed Second Amended Complaint, which included new claims
+Added: against the Company and NeuroOne, Inc for tortious interference with contract and tortious interference with prospective business advantage
+Added: and punitive damages against the Company, NeuroOne Inc.
and Christianson.
−Removed: On June 28, 2019, the Company presented evidence indicating that PMT had participated in a fraud on the Court
−Removed: and sought an Order that PMT had waived the attorney client privilege.
−Removed: On July 16, 2019, the defendants served PMT with
−Removed: a joint notice of motion for sanctions seeking a variety of sanctions for litigation misconduct including, but not limited to, dismissal
−Removed: of the case and an award of attorneys’ fees.
+Added: On June 28, 2019, the Company presented evidence indicating
+Added: that PMT had participated in a fraud on the Court and sought an Order that PMT had waived the attorney client privilege.
+Added: July 16, 2019, the defendants served PMT with a joint notice of motion for sanctions seeking a variety of sanctions for litigation misconduct
+Added: including, but not limited to, dismissal of the case and an award of attorneys’ fees.
The Company, NeuroOne Inc and Mr.
−Removed: Christianson further moved for summary judgment
−Removed: on all remaining claims asserted against them as well as for leave to assert counterclaims against PMT for abuse of process.
−Removed: hearings on the dispositive motions and defendants’ sanctions motion, the district court granted the Company’s motion for
−Removed: sanctions on April 29, 2020.
−Removed: Additionally, the district court granted the Company’s motion for summary judgment in part with respect
−Removed: to the counts for Christianson’s breach of non-confidentiality agreement, and denied the Company’s motion for summary judgment
−Removed: on all other counts.
+Added: further moved for summary judgment on all remaining claims asserted against them as well as for leave to assert counterclaims against
+Added: PMT for abuse of process.
+Added: Following hearings on the dispositive motions and defendants’ sanctions motion, the district court granted
+Added: the Company’s motion for sanctions on April 29, 2020.
+Added: Additionally, the district court granted the Company’s motion for summary
+Added: judgment in part with respect to the counts for Christianson’s breach of non-confidentiality agreement, and denied the Company’s
+Added: motion for summary judgment on all other counts.
NeuroOne Medical Technologies Corporation
−Removed: Notes to Condensed Financial Statements, continued
−Removed: On August 24, 2020, defendants moved the Court
−Removed: to amend their counterclaims for abuse of process against PMT to add a claim for punitive damages with respect to its conduct pertaining
−Removed: to the Fredrickson noncompete.
+Added: Notes to Condensed Financial Statements
+Added: August 24, 2020, defendants moved the Court to amend their counterclaims for abuse of process against PMT to add a claim for punitive
+Added: damages with respect to its conduct pertaining to the Fredrickson noncompete.
On October 12, 2020 the Court awarded NeuroOne, Inc.
−Removed: $ 185,000 in Rule 11 sanctions and Fredrickson
−Removed: $ 145,000 in Rule 11 sanctions with respect to PMT’s misconduct relating to the Fredrickson noncompete.
−Removed: PMT and its former
−Removed: litigation counsel, Barnes & Thornburg, were jointly and severally liable for these awards, which were paid on December 11, 2020
−Removed: and have been recognized in other income in the statements of operations.
−Removed: The Court granted NeuroOne, Inc.’s motion to amend to
−Removed: permit its assertion of the right to assert a punitive damages claim against PMT associated with fighting the allegations relating to
−Removed: the Fredrickson noncompete.
−Removed: On May 27, 2021 PMT moved for summary judgment
−Removed: on defendants’ claims for abuse of process and punitive damages, and on August 5, 2021, the district court granted PMT’s
−Removed: motion to dismiss the abuse of process and punitive damage claims.
−Removed: Trial has been postponed from December 2021 to
−Removed: August of 2022.
−Removed: The Company intends to continue to defend itself vigorously and to continue to aggressively prosecute its affirmative
−Removed: counterclaim against PMT.
−Removed: The outcome of any claim against the Company by PMT was not estimable as of the issuance of these financial
−Removed: Facility Lease
−Removed: Headquarters Lease
−Removed: On October 7, 2019, the Company entered into
−Removed: a non-cancellable lease agreement (the “Lease”) with Biynah Cleveland, LLC, BIP Cleveland, LLC, and Edenvale Investors (together,
−Removed: the “Landlord”) pursuant to which the Company has agreed to lease office space located at 7599 Anagram Drive, Eden Prairie,
−Removed: Minnesota (the “Premises”).
−Removed: The Company took possession of the Premises on November 1, 2019, with the term of the Lease ending
−Removed: 65 months after such date, unless terminated earlier (the “Term”).
−Removed: The initial base rent for the Premises is $6,410 per month
−Removed: for the first 17 months, increasing to $7,076 per month by the end of the Term.
−Removed: In addition, as long as the Company is not in default
−Removed: under the Lease, the Company shall be entitled to an abatement of its base rent for the first 5 months.
−Removed: In addition, the Company will
−Removed: pay its pro rata share of the Landlord’s annual operating expenses associated with the premises, calculated as set forth in the
−Removed: Lease of which the Company is entitled to an abatement of these operating expense for the first 3 months.
−Removed: Los Gatos Lease
−Removed: On July 1, 2021, the Company entered into a non-cancellable
−Removed: facility lease (the “New Lease”), pursuant to which the Company agreed to rent office space for its research and development
−Removed: operations located at 718 University Avenue, Suite #111, Los Gatos, California.
−Removed: The term of the New Lease is eighteen months.
−Removed: space under the New Lease is approximately 1,162 square feet.
+Added: Rule 11 sanctions and Fredrickson $ 145,000 in Rule 11 sanctions with respect to PMT’s misconduct relating to the Fredrickson
+Added: PMT and its former litigation counsel, Barnes & Thornburg, were jointly and severally liable for these awards, which
+Added: were paid on December 11, 2020 and have been recognized in other income in the statements of operations.
+Added: The Court granted NeuroOne,
+Added: Inc.’s motion to amend to permit its assertion of the right to assert a punitive damages claim against PMT associated with fighting
+Added: the allegations relating to the Fredrickson noncompete.
+Added: May 27, 2021 PMT moved for summary judgment on defendants’ claims for abuse of process and punitive damages, and on August 5, 2021,
+Added: the district court granted PMT’s motion to dismiss the abuse of process and punitive damage claims.
+Added: On April 29, 2022, the district court issued an order ruling on several
+Added: motions brought by the parties to exclude evidence from the trial, granting many of the Company’s requests to exclude certain evidence,
+Added: and denying PMT’s exclusion requests.
+Added: has been postponed from December 2021 to August of 2022.
+Added: The Company intends to continue to defend itself vigorously and to continue
+Added: to aggressively prosecute its affirmative counterclaim against PMT.
+Added: The outcome of any claim against the Company by PMT was not estimable
+Added: as of the issuance of these financial statements.
+Added: October 7, 2019, the Company entered into a non-cancellable lease agreement (the “Minnesota Lease”) with Biynah Cleveland,
+Added: LLC, BIP Cleveland, LLC, and Edenvale Investors (together, the “Landlord”) pursuant to which the Company has agreed to lease
+Added: office space located at 7599 Anagram Drive, Eden Prairie, Minnesota (the “Premises”).
+Added: The Company took possession of the
+Added: Premises on November 1, 2019, with the term of the Minnesota Lease ending 65 months after such date, unless terminated earlier (the “Term”).
+Added: The initial base rent for the Premises is $6,410 per month for the first 17 months, increasing to $7,076 per month by the end of the
+Added: In addition, as long as the Company is not in default under the Minnesota Lease, the Company shall be entitled to an abatement
+Added: of its base rent for the first 5 months.
+Added: The Company will also pay its pro rata share of the Landlord’s annual operating expenses
+Added: associated with the premises, calculated as set forth in the Minnesota Lease of which the Company is entitled to an abatement of these
+Added: operating expense for the first 3 months.
+Added: July 1, 2021, the Company entered into a non-cancellable facility lease (the “Los Gatos Lease”), pursuant to which the Company
+Added: agreed to rent office space for its research and development operations located at 718 University Avenue, Suite #111, Los Gatos, California.
+Added: The term of the Los Gatos Lease is eighteen months.
+Added: The facility space under the Los Gatos Lease is approximately 1,162 square feet.
The Company took possession of the office space on July 2, 2021.
−Removed: monthly rent under the New Lease is approximately $ 4,241 .
−Removed: San Jose Lease :
−Removed: On December 30, 2020, the Company entered into
−Removed: a non-cancellable lease agreement for short term office space in San Jose, California (the “San Jose Lease”) for a three
−Removed: month initial term.
−Removed: After March 31, 2021, the San Jose Lease was cancellable upon a 30-day notice to the landlord.
−Removed: The Company took possession
−Removed: of the office space on January 1, 2021 and the San Jose Lease was terminated upon the commencement of the New Lease discussed above.
+Added: The initial monthly rent under the Los Gatos Lease is approximately
+Added: December 30, 2020, the Company entered into a non-cancellable lease agreement for short term office space in San Jose, California (the
+Added: “San Jose Lease”) for a three month initial term.
+Added: After March 31, 2021, the San Jose Lease was cancellable upon a 30-day
+Added: notice to the landlord.
+Added: The Company took possession of the office space on January 1, 2021 and the San Jose Lease was terminated upon
+Added: the commencement of the Los Gatos Lease discussed above.
The base rent under the San Jose Lease was $ 504 per month.
−Removed: During the three months ended December 31, 2021
−Removed: and 2020, rent expense associated with the facility leases amounted to $ 43,045 and $ 29,461 , respectively.
−Removed: Supplemental cash flow information related to
−Removed: the operating leases was as follows:
−Removed: For the three months ended
+Added: the three and six months ended March 31, 2022, rent expense associated with the facility leases amounted to $ 43,085 and $ 86,130 , respectively.
+Added: During the three and six months ended March 31, 2021, rent expense associated with the facility leases amounted to $ 31,800 and $ 61,261 ,
+Added: respectively.
+Added: cash flow information related to the operating leases was as follows:
+Added: six months ended
Cash paid for amounts included in the measurement of lease liability:
3 unchanged sentences
NeuroOne Medical Technologies Corporation
−Removed: Notes to Condensed Financial Statements, continued
−Removed: Supplemental balance sheet information related
−Removed: to the operating leases was as follows:
+Added: Notes to Condensed Financial Statements
+Added: balance sheet information related to the operating leases was as follows:
September 30,
3 unchanged sentences
Weighted average discount rate
−Removed: Maturity of the lease liabilities was as follows:
+Added: of the lease liabilities was as follows:
+Added: Calendar Year
Total lease payments
2 unchanged sentences
Long-term portion
−Removed: NOTE 5 – Supplemental Balance Sheet
−Removed: Prepaid and Other Assets
−Removed: Prepaid and other assets consisted of the following:
+Added: 5 – Supplemental Balance Sheet Information
+Added: and Other Assets
+Added: and other assets consisted of the following:
+Added: March 31, 2022
September 30, 2021
1 unchanged sentence
Deferred offering costs
−Removed: Intangible assets rollforward is as follows:
+Added: assets rollforward is as follows:
Net Intangibles, September 30, 2021
12 - 13 years
−Removed: Net Intangibles, December 31, 2021
−Removed: Amortization expense was $ 5,579 for each of the
−Removed: three month periods ended December 31, 2021 and 2020.
−Removed: Property and Equipment
−Removed: Property and equipment held for use by category
−Removed: are presented in the following table:
+Added: Net Intangibles, March 31, 2022
+Added: expense was $ 5,579 and $ 11,158 for the three and six months ended March 31, 2022, respectively, and $ 5,579 and $ 11,158 for the three
+Added: and six months ended March 31, 2021, respectively.
+Added: NeuroOne Medical Technologies Corporation
+Added: Notes to Condensed Financial Statements
+Added: and Equipment, Net
+Added: and equipment held for use by category are presented in the following table:
+Added: March 31, 2022
September 30,
3 unchanged sentences
Property and equipment, net
−Removed: Depreciation expense was $ 19,582 and $ 13,157
−Removed: for the three month periods ended December 31, 2021 and 2020, respectively.
−Removed: NeuroOne Medical Technologies Corporation
−Removed: Notes to Condensed Financial Statements, continued
−Removed: NOTE 6 - Accrued Expenses and Other Liabilities
−Removed: Accrued expenses consisted of the following at
−Removed: December 31, 2021 and September 30, 2021:
+Added: expense was $ 22,952 and $ 42,534 for the three months and six months ended March 31, 2022, respectively, and $ 13,715 and $ 26,872 for the
+Added: three and six months ended March 31, 2021, respectively.
+Added: 6 - Accrued Expenses and Other Liabilities
+Added: expenses consisted of the following at March 31, 2022 and September 30, 2021:
September 30,
2 unchanged sentences
Royalty Payments
−Removed: The “other” category is primarily
−Removed: comprised of board fees.
−Removed: NOTE 7 – Zimmer Development Agreement
−Removed: On July 20, 2020, the Company entered into an
−Removed: exclusive development and distribution agreement (the “Development Agreement”) with Zimmer, Inc.
−Removed: pursuant to which the Company granted Zimmer exclusive global rights to distribute the Strip/Grid Products and electrode cable assembly
−Removed: products (the “Electrode Cable Assembly Products”).
−Removed: Additionally, the Company granted Zimmer the exclusive right and license
−Removed: to distribute certain depth electrodes developed by the Company (“SEEG Products”, and together with the Strip/Grid Products
−Removed: and Electrode Cable Assembly Products, the “Products”).
−Removed: The parties have agreed to collaborate with respect to development
−Removed: activities under the Development Agreement through a joint development committee composed of an equal number of representatives of Zimmer
−Removed: and the Company.
−Removed: Under the terms of the Development Agreement,
−Removed: the Company is responsible for all costs and expenses related to developing the Products, and Zimmer is responsible for all costs and
−Removed: expenses related to the commercialization of the Products.
−Removed: In addition to the Development Agreement, Zimmer and the Company have entered
−Removed: into a Manufacturing and Supply Agreement (the “MS Agreement”) and a supplier quality agreement (the “Quality Agreement”)
−Removed: with respect to the manufacturing and supply of the Products.
−Removed: Except as otherwise provided in the Development
−Removed: Agreement, the Company is responsible for performing all development activities, including non-clinical and clinical studies directed
−Removed: at obtaining regulatory approval of each Product.
−Removed: Zimmer has agreed to use commercially reasonable efforts to promote, market and sell
−Removed: each Product following the “Product Availability Date” (as defined in the Development Agreement) for such Product.
−Removed: Pursuant to the Development Agreement, Zimmer
−Removed: made an upfront initial exclusivity fee payment of $ 2.0 million (the “Initial Exclusivity Fee”) to the Company.
−Removed: Except where Zimmer timely delivers a Design
−Removed: Modification Notice pursuant to Section 1.2, if one or more of the events set forth below occurs on or before the deadline indicated
−Removed: for such event and the Product Availability Date (as defined in the Development Agreement) for the SEEG Products occurs on or before
−Removed: June 30, 2021, then the Company shall receive the additional amount indicated for such event as part of the SEEG Exclusivity Maintenance
−Removed: ● Design freeze for the SEEG Products by December 15, 2020 - $ 500,000
−Removed: ● Acceptance of all Deliverables for SEEG Products under the Development Plan (as defined in the Development Agreement) by April 30, 2021 - $ 500,000
−Removed: If Zimmer timely delivers a Design Modification
−Removed: Notice to the Company under the Development Agreement, and one or more of the events set forth below occurs on or before the deadline
−Removed: indicated for such event and the Product Availability Date for the SEEG Products occurs on or before June 30, 2021, then the Company
−Removed: shall receive the additional amount indicated for such event as part of the SEEG Exclusivity Maintenance Fee:
−Removed: ● Acceptance of all Deliverables for SEEG Products under the Development Plan other than the Modified Connector by April 30, 2021 - $ 500,000
−Removed: ● Acceptance of all Deliverables for SEEG Products under the Development Plan, including the Modified Connector by September 30, 2021 - $ 500,000
−Removed: For purposes of the Development Agreement, each
−Removed: of the foregoing events shall have occurred only if the Company has demonstrated the achievement of the event to Zimmer’s reasonable
−Removed: satisfaction.
−Removed: Notwithstanding the foregoing, the events in Sections 6.1(c)(ii), (iii) and (iv) of the Development Agreement shall not
−Removed: be deemed to be met if FDA Approval for the SEEG Products is not received prior to the applicable deadline.
+Added: 7 – Zimmer Development Agreement
+Added: July 20, 2020, the Company entered into an exclusive development and distribution agreement (the “Development Agreement”)
+Added: with Zimmer, Inc.
+Added: (“Zimmer”), pursuant to which the Company granted Zimmer exclusive global rights to distribute the Strip/Grid
+Added: Products and electrode cable assembly products (the “Electrode Cable Assembly Products”).
+Added: Additionally, the Company granted
+Added: Zimmer the exclusive right and license to distribute certain depth electrodes developed by the Company (“SEEG Products”,
+Added: and together with the Strip/Grid Products and Electrode Cable Assembly Products, the “Products”).
+Added: The parties have agreed
+Added: to collaborate with respect to development activities under the Development Agreement through a joint development committee composed
+Added: of an equal number of representatives of Zimmer and the Company.
+Added: the terms of the Development Agreement, the Company is responsible for all costs and expenses related to developing the Products, and
+Added: Zimmer is responsible for all costs and expenses related to the commercialization of the Products.
+Added: In addition to the Development Agreement,
+Added: Zimmer and the Company have entered into a Manufacturing and Supply Agreement (the “MS Agreement”) and a supplier quality
+Added: agreement (the “Quality Agreement”) with respect to the manufacturing and supply of the Products.
+Added: as otherwise provided in the Development Agreement, the Company is responsible for performing all development activities, including non-clinical
+Added: and clinical studies directed at obtaining regulatory approval of each Product.
+Added: Zimmer has agreed to use commercially reasonable efforts
+Added: to promote, market and sell each Product following the “Product Availability Date” (as defined in the Development Agreement)
+Added: for such Product.
NeuroOne Medical Technologies Corporation
−Removed: Notes to Condensed Financial Statements, continued
−Removed: In order to maintain the exclusivity of the SEEG
−Removed: Distribution License, Zimmer must pay the SEEG Exclusivity Maintenance Fee to the Company, on or prior to the SEEG Exclusivity Confirmation
−Removed: Date, in immediately available funds as follows:
−Removed: ● if the Product Availability Date for the SEEG Products occurs on or before June 30, 2021, then $ 3,000,000 , plus the amount of any Interim Fee Bonuses earned pursuant to Section 6.1(c), including any such Interim Fee Bonus earned after June 30, 2021 pursuant to Section 6.1(c)(iv) following the delivery of a Design Modification Notice;
−Removed: ● if the Product Availability Date for the SEEG Products occurs after June 30, 2021, but on or before September 30, 2021, then $ 3,000,000 , plus if Zimmer timely issues a Design A-9 Modification Notice, any Interim Fee Bonus earned pursuant to Section 6.1(c)(iv);
−Removed: ● if the Product Availability Date for the SEEG Products occurs after September 30, 2021, but on or before December 31, 2021, then $ 2,500,000 ;
−Removed: ● if the Product Availability Date for the SEEG Products occurs after December 31, 2021, then $ 1,500,000 .
−Removed: The Product Availability Date for the SEEG Products
−Removed: has not yet occurred.
−Removed: Notwithstanding any other provision of the Development Agreement, if the Product Availability Date for the SEEG
−Removed: Products has not occurred on or before June 30, 2022, Zimmer shall have the right to terminate the SEEG Distribution License by delivering
−Removed: written notice to the Company to that effect and, upon delivery of such notice, Zimmer shall be relieved of all of its obligations hereunder
−Removed: with respect to SEEG Products, including any obligation to pay the SEEG Exclusivity Maintenance Fee or to purchase, market, distribute
−Removed: or sell any SEEG Products.
−Removed: The Initial Exclusivity Fee and the SEEG Exclusivity Maintenance Fee (including any Interim Fee Bonus(es)),
−Removed: once paid, are non-refundable.
−Removed: The Development Agreement will expire on the
−Removed: tenth anniversary of the date of the first commercial sale of the last of the Products to achieve a first commercial sale, unless terminated
−Removed: earlier pursuant to its terms.
−Removed: Either party may terminate the Development Agreement (x) with written notice for the other party’s
−Removed: material breach following a cure period or (y) if the other party becomes subject to certain insolvency proceedings.
−Removed: In addition, Zimmer
−Removed: may terminate the Development Agreement for any reason with 90 days’ written notice, and the Company may terminate the Development
−Removed: Agreement if Zimmer acquires or directly or indirectly owns a controlling interest in certain competitors of the Company.
−Removed: At inception of the Zimmer Development Agreement
−Removed: through December 31, 2021, the Company had identified three performance obligations under the Zimmer Development Agreement and consisted
−Removed: of the following:
−Removed: (1) the Company obligation to grant Zimmer access to its intellectual property;
+Added: Notes to Condensed Financial Statements
+Added: to the Development Agreement, Zimmer made an upfront initial exclusivity fee payment of $ 2.0 million (the “Initial Exclusivity
+Added: Fee”) to the Company.
+Added: where Zimmer timely delivers a Design Modification Notice pursuant to Section 1.2, if one or more of the events set forth below occurs
+Added: on or before the deadline indicated for such event and the Product Availability Date (as defined in the Development Agreement) for the
+Added: SEEG Products occurs on or before June 30, 2021, then the Company shall receive the additional amount indicated for such event as part
+Added: of the SEEG Exclusivity Maintenance Fee:
+Added: freeze for the SEEG Products by December 15, 2020 - $ 500,000
+Added: of all Deliverables for SEEG Products under the Development Plan (as defined in the Development Agreement) by April 30, 2021 - $ 500,000
+Added: Zimmer timely delivers a Design Modification Notice to the Company under the Development Agreement, and one or more of the events set
+Added: forth below occurs on or before the deadline indicated for such event and the Product Availability Date for the SEEG Products occurs
+Added: on or before June 30, 2021, then the Company shall receive the additional amount indicated for such event as part of the SEEG Exclusivity
+Added: Maintenance Fee:
+Added: of all Deliverables for SEEG Products under the Development Plan other than the Modified Connector by April 30, 2021 - $ 500,000
+Added: of all Deliverables for SEEG Products under the Development Plan, including the Modified Connector by September 30, 2021 - $ 500,000
+Added: purposes of the Development Agreement, each of the foregoing events shall have occurred only if the Company has demonstrated the achievement
+Added: of the event to Zimmer’s reasonable satisfaction.
+Added: Notwithstanding the foregoing, the events in Sections 6.1(c)(ii), (iii) and (iv)
+Added: of the Development Agreement shall not be deemed to be met if FDA Approval for the SEEG Products is not received prior to the applicable
+Added: order to maintain the exclusivity of the SEEG Distribution License, Zimmer must pay the SEEG Exclusivity Maintenance Fee to the Company,
+Added: on or prior to the SEEG Exclusivity Confirmation Date, in immediately available funds as follows:
+Added: the Product Availability Date for the SEEG Products occurs on or before June 30, 2021, then $ 3,000,000 , plus the amount of any Interim
+Added: Fee Bonuses earned pursuant to Section 6.1(c), including any such Interim Fee Bonus earned after June 30, 2021 pursuant to Section 6.1(c)(iv)
+Added: following the delivery of a Design Modification Notice;
+Added: the Product Availability Date for the SEEG Products occurs after June 30, 2021, but on or before September 30, 2021, then $ 3,000,000 ,
+Added: plus if Zimmer timely issues a Design A-9 Modification Notice, any Interim Fee Bonus earned pursuant to Section 6.1(c)(iv);
+Added: the Product Availability Date for the SEEG Products occurs after September 30, 2021, but on or before December 31, 2021, then $ 2,500,000 ;
+Added: the Product Availability Date for the SEEG Products occurs after December 31, 2021, then $ 1,500,000 .
+Added: Product Availability Date for the SEEG Products has not yet occurred.
+Added: Notwithstanding any other provision of the Development Agreement,
+Added: if the Product Availability Date for the SEEG Products has not occurred on or before June 30, 2022, Zimmer shall have the right to terminate
+Added: the SEEG Distribution License by delivering written notice to the Company to that effect and, upon delivery of such notice, Zimmer shall
+Added: be relieved of all of its obligations hereunder with respect to SEEG Products, including any obligation to pay the SEEG Exclusivity Maintenance
+Added: Fee or to purchase, market, distribute or sell any SEEG Products.
+Added: The Initial Exclusivity Fee and the SEEG Exclusivity Maintenance Fee
+Added: (including any Interim Fee Bonus(es)), once paid, are non-refundable.
+Added: NeuroOne Medical Technologies Corporation
+Added: Notes to Condensed Financial Statements
+Added: Development Agreement will expire on the tenth anniversary of the date of the first commercial sale of the last of the Products to achieve
+Added: a first commercial sale, unless terminated earlier pursuant to its terms.
+Added: Either party may terminate the Development Agreement (x) with
+Added: written notice for the other party’s material breach following a cure period or (y) if the other party becomes subject to certain
+Added: insolvency proceedings.
+Added: In addition, Zimmer may terminate the Development Agreement for any reason with 90 days’ written notice,
+Added: and the Company may terminate the Development Agreement if Zimmer acquires or directly or indirectly owns a controlling interest in certain
+Added: competitors of the Company.
+Added: inception of the Zimmer Development Agreement through March 31, 2022, the Company had identified three performance obligations under
+Added: the Zimmer Development Agreement and consisted of the following:
+Added: (1) the Company obligation to grant Zimmer access to its intellectual
(2) complete SEEG Product development;
and (3) complete Strip/Grid Product development.
−Removed: Accordingly, the Company recognized revenue in the amount of $ 6,374 and $ 22,274 related
−Removed: to the development of the Products completed during the three month periods ended December 31, 2021 and 2020, respectively, in connection
−Removed: with the Initial Exclusivity Fee payment.
−Removed: The Zimmer Development Agreement was accounted for under the provisions of ASC 606, Revenue
−Removed: from Contracts with Customers.
−Removed: A reconciliation of the closing balance of deferred
−Removed: revenue related to the Zimmer Development Agreement is as follows during the three months ended as of December 31, 2021 and 2020:
+Added: Accordingly, the Company recognized
+Added: revenue in the amount of zero and $ 20,113 during the three month periods ended March 31, 2022 and 2021, respectively, and $ 6,374 and
+Added: $ 42,387 during the six month periods ending March 31, 2022 and 2021, respectively, in connection with the Initial Exclusivity Fee payment.
+Added: The Zimmer Development Agreement was accounted for under the provisions of ASC 606, Revenue from Contracts with Customers.
+Added: reconciliation of the closing balance of deferred revenue related to the Zimmer Development Agreement is as follows during the six months
+Added: ended as of March 31, 2022 and 2021:
Deferred Revenue
1 unchanged sentence
Revenue recognized
−Removed: Balance as of end of period – December 31
−Removed: The remaining performance obligations reflected
−Removed: in deferred revenue as of December 31, 2021 are expected to be completed in the first half of fiscal year 2022.
−Removed: Product Revenue
−Removed: Product revenue recognized during the three month
−Removed: periods ended December 31, 2021 and 2020 was $ 33,748 and $ 71,474 , respectively, related to its Strip/Grid Products, SEEG Products and
−Removed: Electrode Cable Assembly Products.
−Removed: Advertising Expense
−Removed: Advertising expense is charged to selling, general
−Removed: and administrative expenses during the period that it is incurred.
−Removed: Total advertising expense amounted to $ 61,335 and $ 29,007 for the
−Removed: three month periods ended December 31, 2021 and 2020, respectively.
−Removed: NOTE 8 - Convertible Promissory Notes and
−Removed: Warrant Agreements
+Added: Balance as of end of period – March 31
+Added: remaining performance obligations reflected in deferred revenue as of March 31, 2022 are expected to be completed in the second half
+Added: of fiscal year 2022.
+Added: revenue related to its Strip/Grid Products, SEEG Products and Electrode Cable Assembly Products.
+Added: Product revenue recognized during the
+Added: three and six month periods ended March 31, 2022 was $ 36,584 and $ 70,332 , respectively.
+Added: Product revenue recognized during the three and
+Added: six month periods ended March 31, 2021 was $ 18,240 and $ 89,714 , respectively.
+Added: expense is charged to selling, general and administrative expenses during the period that it is incurred.
+Added: Total advertising expense amounted
+Added: to $ 113,197 and $ 174,532 for the three and six month periods ended March 31, 2022, respectively.
+Added: Total advertising expense amounted to
+Added: $ 113,140 and $ 142,147 for the three and six month periods ended March 31, 2021, respectively.
+Added: 8 - Convertible Promissory Notes and Warrant Agreements
Paulson Convertible Note Offering
−Removed: On November 1, 2019, the Company entered into
−Removed: a subscription agreement with certain accredited investors, pursuant to which the Company, in a private placement (the “2019 Paulson
−Removed: Private Placement”), agreed to issue and sell to the investors 13 % convertible promissory notes (each, a “2019 Paulson Note”
−Removed: and collectively, the “2019 Paulson Notes”) and warrants (each, a “2019 Paulson Warrant” and collectively, the
−Removed: “2019 Paulson Warrants”) to purchase shares of the Company’s common stock.
+Added: November 1, 2019, the Company entered into a subscription agreement with certain accredited investors, pursuant to which the Company,
+Added: in a private placement (the “2019 Paulson Private Placement”), agreed to issue and sell to the investors 13 % convertible
+Added: promissory notes (each, a “2019 Paulson Note” and collectively, the “2019 Paulson Notes”) and warrants (each,
+Added: a “2019 Paulson Warrant” and collectively, the “2019 Paulson Warrants”) to purchase shares of the Company’s
+Added: common stock.
NeuroOne Medical Technologies Corporation
−Removed: Notes to Condensed Financial Statements, continued
−Removed: The initial closing of the 2019 Paulson Private
−Removed: Placement was consummated on November 1, 2019, and, on that date and through December 3, 2019, the Company issued the 2019 Paulson Notes
−Removed: in an aggregate principal amount of $ 3,234,800 to the subscribers for gross proceeds equaling the principal amount.
−Removed: The 2019 Paulson
−Removed: Private Placement terminated on December 3, 2019.
−Removed: On April 24, 2020, the Company and holders of
−Removed: a majority in aggregate principal amount of the 2019 Paulson Notes entered into an amendment to the 2019 Paulson Notes (the “Second
−Removed: 2019 Paulson Notes Amendment”) to, among other things:
+Added: Notes to Condensed Financial Statements
+Added: initial closing of the 2019 Paulson Private Placement was consummated on November 1, 2019, and, on that date and through December 3,
+Added: 2019, the Company issued the 2019 Paulson Notes in an aggregate principal amount of $ 3,234,800 to the subscribers for gross proceeds
+Added: equalling the principal amount.
+Added: The 2019 Paulson Private Placement terminated on December 3, 2019.
+Added: April 24, 2020, the Company and holders of a majority in aggregate principal amount of the 2019 Paulson Notes entered into an amendment
+Added: to the 2019 Paulson Notes (the “Second 2019 Paulson Notes Amendment”) to, among other things:
Extended the Maturity
4 unchanged sentences
upon the a subscriber’s optional conversion of the 2019 Paulson Notes prior to a 2019 Qualified Financing (as defined in the
−Removed: 2019 Paulson Notes) would have equaled:
+Added: 2019 Paulson Notes) would have equalled:
(1) the Outstanding Balance as defined below of such subscriber’s 2019 Paulson Note
10 unchanged sentences
the resale of any common stock received on conversion of such 2019 Paulson Notes, and shares of common stock underlying the Warrants.
−Removed: The 2019 Paulson Notes had a fixed interest rate
−Removed: of 13 % per annum and required the Company to repay the principal and accrued and unpaid interest thereon on November 1, 2020 (the “Maturity
−Removed: Interest on principal amounted to $ 5,701 during the three month periods ended December 31, 2020 and was recorded under
−Removed: the net valuation change of instruments measured at fair value in the condensed statements of operations.
−Removed: The 2019 Paulson Notes were
−Removed: not outstanding during the three month period ended December 31, 2021.
−Removed: The Company elected to account for the 2019 Paulson
−Removed: Notes on a fair value basis under ASC 825 to comprehensively value and streamline the accounting for the embedded conversion options.
−Removed: Subsequent to issuance, the fair value change of the Paulson Notes amounted to a benefit of $( 1,974 ) during the three months ended December
−Removed: 31, 2020 and was recorded under the net valuation change of instruments measured at fair value in the condensed statements of operations.
−Removed: Each 2019 Paulson Warrant grants the holder the
−Removed: option to purchase the number of shares of common stock equal to (i) 0.5 multiplied by (ii) the principal amount of such subscriber’s
−Removed: 2019 Paulson Notes divided by 5.61, with an exercise price per share equal to $5.61.
−Removed: As of the final closing on December 3, 2019, the
−Removed: Company issued 2019 Paulson Warrants exercisable for 288,305 shares of common stock in connection with all closings of the 2019 Paulson
−Removed: Private Placement.
−Removed: The 2019 Paulson Warrants are immediately exercisable and expire on November 1, 2022 .
−Removed: The exercise price is subject
−Removed: to adjustment in the event of any stock dividends or splits, reverse stock split, recapitalization, reorganization or similar transaction,
−Removed: as described therein.
−Removed: The 2019 Paulson warrants were deemed to be a free-standing instrument and were accounted for as equity.
−Removed: that the fair value of the 2019 Paulson Notes exceeded the proceeds received at issuance, there was no value attributed to the 2019 Paulson
−Removed: Warrants in the condensed financial statements.
−Removed: Issuance costs during the three month period
−Removed: ended December 31, 2020 in connection with the 2019 Paulson Private Placement were $ 3,053 and related to legal costs.
−Removed: The issuance costs
−Removed: were recorded as a component of interest in the accompanying condensed statements of operations.
−Removed: During the first quarter of fiscal year 2021,
−Removed: the remaining holders of the 2019 Paulson Notes elected to convert the remaining outstanding principal and accrued and unpaid interest
−Removed: in the amount of $ 615,159 into 292,754 shares of common stock.
−Removed: NOTE 9 – Stock-Based Compensation
−Removed: During the three month periods ended December
−Removed: 31, 2021 and 2020, stock-based compensation expense was included in general and administrative and research and development costs as
−Removed: follows in the accompanying condensed statements of operations.
+Added: 2019 Paulson Notes had a fixed interest rate of 13 % per annum and required the Company to repay the principal and accrued and unpaid
+Added: interest thereon on November 1, 2020 (the “Maturity Date”).
+Added: Interest on principal amounted to $ 5,701 during the six month
+Added: period ended March 31, 2021 and was recorded under the net valuation change of instruments measured at fair value in the condensed statements
+Added: of operations.
+Added: The 2019 Paulson Notes were not outstanding during the six month period ended March 31, 2022.
+Added: Company elected to account for the 2019 Paulson Notes on a fair value basis under ASC 825 to comprehensively value and streamline the
+Added: accounting for the embedded conversion options.
+Added: Subsequent to issuance, the fair value change of the Paulson Notes amounted to a benefit
+Added: of $( 1,974 ) during the six months ended March 31, 2021 and was recorded under the net valuation change of instruments measured at fair
+Added: value in the condensed statements of operations.
+Added: 2019 Paulson Warrant grants the holder the option to purchase the number of shares of common stock equal to (i) 0.5 multiplied by (ii)
+Added: the principal amount of such subscriber’s 2019 Paulson Notes divided by 5.61, with an exercise price per share equal to $5.61.
+Added: As of the final closing on December 3, 2019, the Company issued 2019 Paulson Warrants exercisable for 288,305 shares of common stock
+Added: in connection with all closings of the 2019 Paulson Private Placement.
+Added: The 2019 Paulson Warrants are immediately exercisable and expire
+Added: on November 1, 2022 .
+Added: The exercise price is subject to adjustment in the event of any stock dividends or splits, reverse stock split,
+Added: recapitalization, reorganization or similar transaction, as described therein.
+Added: The 2019 Paulson warrants were deemed to be a free-standing
+Added: instrument and were accounted for as equity.
+Added: Given that the fair value of the 2019 Paulson Notes exceeded the proceeds received at issuance,
+Added: there was no value attributed to the 2019 Paulson Warrants in the condensed financial statements.
+Added: NeuroOne Medical Technologies Corporation
+Added: Notes to Condensed Financial Statements
+Added: costs during the six month period ended March 31, 2021 in connection with the 2019 Paulson Private Placement were $ 3,053 and related
+Added: to legal costs.
+Added: The issuance costs were recorded as a component of interest in the accompanying condensed statements of operations.
+Added: the first quarter of fiscal year 2021, the remaining holders of the 2019 Paulson Notes elected to convert the remaining outstanding principal
+Added: and accrued and unpaid interest in the amount of $ 615,159 into 292,754 shares of common stock.
+Added: 9 – Stock-Based Compensation
+Added: the three and six month periods ended March 31, 2022 and 2021, stock-based compensation expense related to stock-based awards was included
+Added: in general and administrative and research and development costs as follows in the accompanying condensed statements of operations.
+Added: Three Months Ended
+Added: Six Months Ended
General and administrative
1 unchanged sentence
Total stock-based compensation expense
−Removed: Stock Options
−Removed: During the three month period ended December
−Removed: 31, 2021 and 2020, under the 2017 Equity Incentive Plan (the “2017 Plan”), the Company granted 2,000 and 41,669 stock options,
−Removed: respectively, to its employees and consultants.
−Removed: Vesting generally occurs over an immediate to 48 month period based on a time of service
−Removed: The grant date fair value of the grants issued during the three month periods ended December 31, 2021 and 2020 was $ 1.72 and
−Removed: $ 1.60 per share, respectively.
−Removed: The total expense for the three months ended December 31, 2021 and 2020 related to stock options was $ 162,361
−Removed: and $ 100,147 , respectively.
−Removed: The total number of stock options outstanding as of December 31, 2021 and September 30, 2021 was 1,111,226
−Removed: and 1,122,560 , respectively.
−Removed: NeuroOne Medical Technologies Corporation
−Removed: Notes to Condensed Financial Statements, continued
−Removed: The weighted-average assumptions used in the
−Removed: Black-Scholes option-pricing model are as follows for the stock options granted during the three month period ended December 31, 2021
+Added: the three month periods ended March 31, 2022 and 2021, under the 2017 Equity Incentive Plan (the “2017 Plan”), the Company
+Added: granted 60,000 and 580,002 stock options, respectively, to its officers and employees.
+Added: During the six month periods ended March 31, 2022
+Added: and 2021, the Company granted 62,000 and 621,671 , respectively, to its officers, employees and consultants.
+Added: Vesting generally occurs
+Added: over an immediate to 48 month period based on a time of service condition although vesting acceleration is provided under one grant in
+Added: the event that a certain milestone is met.
+Added: The grant date fair value of the grants issued during the three month periods ended March
+Added: 31, 2022 and 2021 was $ 1.00 and $ 3.02 per share, respectively.
+Added: The grant date fair value of the grants issued during the six month periods
+Added: ended March 31, 2022 and 2021 was $ 1.03 and $ 2.92 per share, respectively.
+Added: total expense for the three months ended March 31, 2022 and 2021 related to stock options was $ 145,421 and $ 217,466 , respectively.
+Added: total expense for the six months ended March 31, 2022 and 2021 related to stock options was $ 307,782 and $ 317,612 , respectively.
+Added: total number of stock options outstanding as of March 31, 2022 and September 30, 2021 was 1,162,059 and 1,122,560 , respectively.
+Added: weighted-average assumptions used in the Black-Scholes option-pricing model are as follows for the stock options granted during the three
+Added: and six month period ended March 31, 2022 and 2021:
+Added: Three Months Ended
+Added: Six Months Ended
Expected stock price volatility
2 unchanged sentences
Risk free interest rate
−Removed: During the three month periods ended December
−Removed: 31, 2021 and 2020, 18,843 and 71,774 stock options vested, and 13,334 and zero stock options were forfeited during these periods, respectively.
−Removed: Restricted Stock Units
−Removed: There were no restricted stock units (“RSUs”)
−Removed: granted during the three months ended December 31, 2021 and 2020, 5,644 and 8,384 RSUs vested during these periods, respectively.
−Removed: total expense for the three months ended December 31, 2021 and 2020 related to these RSUs was $ 40,711 and $ 43,082 , respectively.
−Removed: were forfeited during the three month periods ended December 31, 2021 and 2020.
−Removed: Other Stock-Based Awards
−Removed: In August 2020, an additional consulting agreement
−Removed: was executed whereby 40,000 shares of common stock were issued, subject to Company repurchase.
−Removed: The stock award under the agreement vested
−Removed: over a six-month period.
−Removed: As of December 31, 2020, 26,667 shares were vested under this agreement of which 20,000 shares vested during
−Removed: the first quarter of fiscal year 2021.
−Removed: Compensation expense related to the stock awards granted under this consulting agreement amounted
−Removed: to $102,600 for the three month ended December 31, 2020 and was included in the total stock-based expense.
−Removed: No stock-based awards were issued during the
−Removed: first quarter of fiscal year 2022 and no expense associated with stock awards was recorded during the three months ended December 31,
−Removed: Inducement Plan
−Removed: On October 4, 2021, the Company adopted the NeuroOne
−Removed: Medical Technologies Corporation 2021 Inducement Plan (the “Plan”), pursuant to which the Company reserved 420,350 shares
−Removed: of its common stock to be used exclusively for grants of awards to individuals who were not previously employees or directors of the
−Removed: Company, as an inducement material to the individual’s entry into employment with the Company within the meaning of Rule 5635(c)(4)
−Removed: of the Nasdaq Listing Rules.
−Removed: The Plan was approved by the Company’s Board of Directors without stockholder approval in accordance
−Removed: with such rule.
−Removed: As of December 31, 2021, 673,022 shares were
−Removed: available in the aggregate for future issuance under the 2017 Equity Incentive Plan and Inducement Plan.
−Removed: No shares were available for
−Removed: future issuance under the 2016 Equity Incentive Plan.
−Removed: Unrecognized stock-based compensation was $ 1,473,086 as of December 31, 2021.
−Removed: unrecognized share-based expense is expected to be recognized over a weighted average period of 2.7 years.
−Removed: NOTE 10 – Concentrations
−Removed: Financial instruments that potentially subject
−Removed: the Company to a concentration of credit risk consist of cash.
−Removed: The Company’s cash is held by a network of financial institutions
−Removed: in the United States.
+Added: the three month periods ended March 31, 2022 and 2021, 182,217 and 34,752 stock options vested, respectively, and 9,167 and 10,146 stock
+Added: options were forfeited during these periods, respectively.
+Added: During the six month periods ended March 31, 2022 and 2021, 201,060 and 106,527
+Added: stock options vested, respectively and 22,501 and 10,146 stock options were forfeited during these periods, respectively.
+Added: three and six months ended March 31, 2021, 758 stock options were exercised with an intrinsic value of $ 955 .
+Added: No options were exercised
+Added: during the three and six months ended March 31, 2022.
+Added: NeuroOne Medical Technologies Corporation
+Added: Notes to Condensed Financial Statements
+Added: the three and six months ended March 31, 2022, the Company granted an aggregate of 355,950 restricted stock units (“RSUs”)
+Added: to certain officers and employees under the 2017 Plan.
+Added: The weighted average grant date fair value of the RSU granted during the three
+Added: and six months ended March 31, 2022 was $ 2.10 per unit.
+Added: The RSUs vest over a three year period with 50 percent vesting on the first anniversary
+Added: of the grant date and the remaining RSUs vesting in equal monthly installments on the last day of each month over 24 months, subject
+Added: to the recipient’s continued service on such dates.
+Added: No RSUs were granted during the three and six month periods ended March
+Added: the three months ended March 31, 2022 and 2021, 3,444 and 7,992 RSUs vested, respectively, and no RSUs were forfeited during these periods.
+Added: During the six months ended March 31, 2022 and 2021, 9,088 and 16,376 RSUs vested, respectively, and no RSUs were forfeited during these
+Added: The total expense for the three months ended March 31, 2022 and 2021 related to these RSUs was $ 87,295 and $ 40,493 , respectively.
+Added: The total expense for the six months ended March 31, 2022 and 2021 related to these RSUs was $ 128,006 and $ 83,576 , respectively.
+Added: Stock-Based Awards
+Added: August 2020, an additional consulting agreement was executed whereby 40,000 shares of common stock were issued, subject to Company repurchase.
+Added: The stock award under the agreement vested over a six-month period.
+Added: As of March 31, 2021, 40,000 shares were vested under this agreement
+Added: of which 13,334 and 33,334 shares vested during the three and six month periods ended March 31, 2021, respectively.
+Added: Compensation expense
+Added: related to the stock award granted under this consulting agreement amounted to $68,400 and $171,000 for the three and six months ended
+Added: March 31, 2021, respectively, and was included in the total stock-based compensation expense.
+Added: other stock-based awards were issued during the three and six month periods ended March 31, 2022 and no expense associated with stock
+Added: awards was recorded during the three and six months ended March 31, 2022.
+Added: October 4, 2021, the Company adopted the NeuroOne Medical Technologies Corporation 2021 Inducement Plan (the “Inducement Plan”),
+Added: pursuant to which the Company reserved 420,350 shares of its common stock to be used exclusively for grants of awards to individuals
+Added: who were not previously employees or directors of the Company, as an inducement material to the individual’s entry into employment
+Added: with the Company within the meaning of Rule 5635(c)(4) of the Nasdaq Listing Rules.
+Added: The Inducement Plan was approved by the Company’s
+Added: Board of Directors without stockholder approval in accordance with such rule.
+Added: Plan Evergreen Provision
+Added: the 2017 Plan, the shares reserved automatically increase on January 1st of each year, for a period of not more than ten years from the
+Added: date the 2017 Plan is approved by the stockholders of the Company, commencing on January 1, 2019 and ending on (and including) January
+Added: 1, 2027, to an amount equal to 13% of the fully-diluted shares outstanding as of December 31st of the preceding calendar year.
+Added: Notwithstanding
+Added: the foregoing, the Board may act prior to January 1st of a given year to provide that there will be no January 1st increase in the share
+Added: reserve for such year or that the increase in the share reserve for such year will be a lesser number of shares of common stock than
+Added: would otherwise occur pursuant to the preceding sentence.
+Added: “Fully Diluted Shares” as of a date means an amount equal to the
+Added: number of shares of common stock (i) outstanding and (ii) issuable upon exercise, conversion or settlement of outstanding awards under
+Added: the 2017 Plan and any other outstanding options, warrants or other securities of the Company that are (directly or indirectly) convertible
+Added: or exchangeable into or exercisable for shares of common stock, in each case as of the close of business of the Company on December 31
+Added: of the preceding calendar year.
+Added: Effective January 1, 2022, 1,614,538 shares were added to the 2017 Plan as a result of the evergreen
+Added: NeuroOne Medical Technologies Corporation
+Added: Notes to Condensed Financial Statements
+Added: of March 31, 2022, 1,880,777 shares were available in the aggregate for future issuance under the 2017 Plan and Inducement Plan.
+Added: were available for future issuance under the 2016 Equity Incentive Plan.
+Added: Unrecognized stock-based compensation was $ 2,035,046 as of March
+Added: The unrecognized share-based expense is expected to be recognized over a weighted average period of 2.6 years.
+Added: 10 – Concentrations
+Added: instruments that potentially subject the Company to a concentration of credit risk consist of cash.
+Added: The Company’s cash is held
+Added: by a network of financial institutions in the United States.
Amounts on deposit may at times exceed federally insured limits.
−Removed: The Company has not experienced any losses on
−Removed: its deposits since inception, and management believes that minimal credit risk exists with respect to these financial institutions.
−Removed: of December 31, 2021, the Company had no deposits in excess of federally insured amounts.
−Removed: One customer accounts for all of the Company’s product and collaborations
−Removed: Supplier concentration
−Removed: One contract manufacturer produces all of the Company’s Strip/Grid
−Removed: Products and SEEG Products.
−Removed: NOTE 11 – Income Taxes
−Removed: The effective tax rate for the three months ended
−Removed: December 31, 2021 and 2020 was zero percent.
−Removed: As a result of the analysis of all available evidence as of December 31, 2021 and September
−Removed: 30, 2021, the Company recorded a full valuation allowance on its net deferred tax assets.
−Removed: Consequently, the Company reported no income
−Removed: tax benefit during the three months ended December 31, 2021 and 2020.
−Removed: If the Company’s assumptions change and the Company
−Removed: believes that it will be able to realize these deferred tax assets, the tax benefits relating to any reversal of the valuation allowance
−Removed: on deferred tax assets will be recognized as a reduction of future income tax expense.
−Removed: If the assumptions do not change, each
−Removed: period the Company could record an additional valuation allowance on any increases in the deferred tax assets.
+Added: has not experienced any losses on its deposits since inception, and management believes that minimal credit risk exists with respect
+Added: to these financial institutions.
+Added: As of March 31, 2022, the Company had no deposits in excess of federally insured amounts.
+Added: customer accounts for all of the Company’s product and collaborations revenue.
+Added: concentration
+Added: contract manufacturer produces all of the Company’s Strip/Grid Products and SEEG Products.
+Added: 11 – Income Taxes
+Added: effective tax rate for the three and six months ended March 31, 2022 and 2021 was zero percent.
+Added: As a result of the analysis of all available
+Added: evidence as of March 31, 2022 and September 30, 2021, the Company recorded a full valuation allowance on its net deferred
+Added: Consequently, the Company reported no income tax benefit during the three and six months ended March
+Added: 31, 2022 and 2021.
+Added: If the Company’s assumptions change and the Company believes that it will be able to realize these deferred
+Added: tax assets, the tax benefits relating to any reversal of the valuation allowance on deferred tax assets will be recognized as a reduction
+Added: of future income tax expense.
+Added: If the assumptions do not change, each period the Company could record an additional valuation
+Added: allowance on any increases in the deferred tax assets.
+Added: 12 – Stockholders’ Equity
+Added: October 13, 2021, the Company, entered into an Underwriting Agreement (the “Underwriting Agreement”) with Craig-Hallum
+Added: Capital Group LLC, as underwriter (the “Underwriter”), relating to the issuance and sale of 3,750,000 shares of the Company’s
+Added: common stock at a price to the public of $ 3.20 per share.
+Added: In addition, under the terms of the Underwriting Agreement, the Company granted
+Added: the Underwriter an option, exercisable for 30 days, to purchase up to an additional 562,500 shares of common stock on the same terms.
+Added: The base offering closed on October 15, 2021, and the sale of 422,057 shares of common stock subject to the Underwriter’s overallotment
+Added: option closed on November 15, 2021.
+Added: gross proceeds to the Company from this offering were approximately $ 13.4 million prior to deducting underwriting discounts and
+Added: other offering expenses payable by the Company in the amount of approximately $ 1.4 million in the aggregate.
NeuroOne Medical Technologies Corporation
−Removed: Notes to Condensed Financial Statements, continued
−Removed: NOTE 12 – Stockholders’ Equity
−Removed: Public Offering
−Removed: On October 13, 2021, the Company, entered
−Removed: into an Underwriting Agreement (the “Underwriting Agreement”) with Craig-Hallum Capital Group LLC, as underwriter (the “Underwriter”),
−Removed: relating to the issuance and sale of 3,750,000 shares of the Company’s common stock at a price to the public of $ 3.20 per share.
−Removed: In addition, under the terms of the Underwriting Agreement, the Company granted the Underwriter an option, exercisable for 30 days, to
−Removed: purchase up to an additional 562,500 shares of common stock on the same terms.
−Removed: The base offering closed on October 15, 2021, and the
−Removed: sale of 422,057 shares of common stock subject to the Underwriter’s overallotment option closed on November 15, 2021.
−Removed: The gross proceeds to the Company from this offering
−Removed: were approximately $ 13.4 million prior to deducting underwriting discounts and other offering expenses payable by the Company in
−Removed: the amount of approximately $ 1.4 million in the aggregate.
+Added: Notes to Condensed Financial Statements
Private Placement
−Removed: On January 12, 2021, the Company entered into
−Removed: a Common Stock and Warrant Purchase Agreement (the “2021 Purchase Agreement”) with certain accredited investors (the “Purchasers”),
−Removed: pursuant to which the Company, in the 2021 Private Placement, agreed to issue and sell an aggregate of 4,166,682 shares (the “Shares”)
−Removed: of the common stock of the Company, par value $ 0.001 per share (the “Common Stock”), and warrants to purchase an aggregate
+Added: January 12, 2021, the Company entered into a Common Stock and Warrant Purchase Agreement with certain accredited investors (the “Purchasers”),
+Added: pursuant to which the Company agreed to issue and sell an aggregate of 4,166,682 shares common stock, and warrants to purchase an aggregate
of 4,166,682 shares of Common Stock (the “2021 Warrants”) at an aggregate purchase price of $ 3.00 per share of Common Stock
4 unchanged sentences
The 2021 Private Placement closed on January 14, 2021.
−Removed: Warrant Activity and Summary
−Removed: The following table summarizes warrant activity
−Removed: during the three month period ended December 31, 2021:
+Added: Activity and Summary
+Added: following table summarizes warrant activity during the six month period ended March 31, 2022:
Outstanding and exercisable at September 30, 2021
1 unchanged sentence
Forfeited/Expired
−Removed: Outstanding and exercisable at December 31, 2021
+Added: Outstanding and exercisable at March 31, 2022
$ 5.25 -$ 9.00
−Removed: NOTE 13 – Subsequent Events
−Removed: 2017 Plan Evergreen Provision
−Removed: Under the 2017 Plan, the shares reserved automatically
−Removed: increase on January 1st of each year, for a period of not more than ten years from the date the 2017 Plan is approved by the stockholders
−Removed: of the Company, commencing on January 1, 2019 and ending on (and including) January 1, 2027, to an amount equal to 13 % of the fully-diluted
−Removed: shares outstanding as of December 31st of the preceding calendar year.
−Removed: Notwithstanding the foregoing, the Board may act prior to January
−Removed: 1st of a given year to provide that there will be no January 1st increase in the share reserve for such year or that the increase in
−Removed: the share reserve for such year will be a lesser number of shares of common stock than would otherwise occur pursuant to the preceding
−Removed: “Fully Diluted Shares” as of a date means an amount equal to the number of shares of common stock (i) outstanding
−Removed: and (ii) issuable upon exercise, conversion or settlement of outstanding awards under the 2017 Plan and any other outstanding options,
−Removed: warrants or other securities of the Company that are (directly or indirectly) convertible or exchangeable into or exercisable for shares
−Removed: of common stock, in each case as of the close of business of the Company on December 31 of the preceding calendar year.
−Removed: Effective January
−Removed: 1, 2022, 1,614,538 shares were added to the 2017 Plan as a result of the evergreen provision.
−Removed: Stock-Based Awards
−Removed: On February 3, 2022, the Company granted an aggregate
−Removed: of 355,950 RSUs to certain officers and employees under the 2017 Plan.
−Removed: The RSUs vest over a three year period with 50 percent vesting
−Removed: on the first anniversary of the grant date and the remaining RSUs vesting in equal monthly installments on the last day of each month
−Removed: over 24 months, subject to the recipient’s continued service on such dates.
+Added: 13 – Deferred Contribution Plan
+Added: Company has a 401(k) defined contribution plan (the “401K Plan”) for all employees over age 21.
+Added: Employees can defer up to
+Added: 100 % of their compensation through payroll withholdings into the 401K Plan subject to federal law limits.
+Added: The Company may match 100 %
+Added: of deferrals up to 3 % of one’s contributions.
+Added: The Company’s matching contributions to employee deferrals are discretionary.
+Added: The Company may also make discretionary profit sharing contributions under the 401K Plan in the future, but it has not done so through
+Added: March 31, 2022.
+Added: contributions and any employer matching contributions made to satisfy certain non-discrimination tests required by the Internal Revenue
+Added: Code are 100 % vested upon contribution.
+Added: Discretionary employer matches to employee deferrals vest over a six year period beginning on
+Added: the second anniversary of an employee’s date of hire.
+Added: Discretionary profit sharing contributions vest over a five year period beginning
+Added: on the first anniversary of an employee’s date of hire.
+Added: The amount of matching contributions to the 401K Plan to satisfy certain
+Added: non-discrimination tests was $ 30,697 and $ 14,803 during the three and six month periods ending March 31, 2022 and 2021, respectively.
+Added: 14 – Subsequent Events
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.