The Company has not generated any revenues and has incurred significant losses since inception. For the three months endedMarch 31, 2022 , the Company had net income of$1,563,713 and used cash in operations of$2,072,931 . As ofMarch 31, 2022 , the Company has an accumulated deficit of$67,118,573 and a working capital deficit of$6,120,408 . The Company expects to invest a significant amount of capital to fund research and development. As a result, the Company expects that its operating expenses will increase significantly, and consequently will require significant revenues to become profitable. Even if the Company does become profitable, it may not be able to sustain or increase profitability on a quarterly or annual basis. The Company cannot predict when, if ever, it will be profitable. There can be no assurance that the intellectual property of the Company, or other technologies it may acquire, will meet applicable regulatory standards, obtain required regulatory approvals, be capable of being produced in commercial quantities at reasonable costs, or be successfully marketed. The Company plans to undertake additional laboratory studies with respect to the intellectual property, and there can be no assurance that the results from such studies or trials will result in a commercially viable product or will not identify unwanted side effects. A worsening of the levels of market disruption and volatility seen in the recent past as the result of the COVID-19 pandemic could have an adverse effect on the Company's ability to access capital, on the Company's business, results of operations and financial condition. Management continues to monitor the developments and has taken active measures to protect the health of the Company's employees, their families and the Company's communities. The ultimate impact will depend heavily on the duration of the COVID-19 pandemic and public health responses, including seasonal outbreaks, the efficacy of vaccines, the effect of mutations of the virus on such efficacy, the availability of vaccines and boosters, and the willingness of individuals to receive such vaccines and boosters, as well as the substance and pace of macroeconomic recovery, all of which are uncertain and difficult to predict considering the continuing evolving landscape of the COVID-19 pandemic and the public health responses to contain it. 6
Management has evaluated, and will continue to evaluate, the impact of the COVID-19 pandemic on the industry and has concluded that while it is reasonably possible that the virus could have a negative effect on the Company's financial position or results of its operations, the specific impact is not readily determinable as of the date of these unaudited condensed consolidated financial statements (the "condensed consolidated financial statements"). The follow-up time for patient data and the statistical analysis for the Phase 2b Dupuytren's Contracture clinical trial was delayed as a result of COVID-19, but such follow-up and statistical analyses are now complete. The Company announced the top-line data results from the Phase 2b trial onDecember 1, 2021 and the data was published onApril 29, 2022 in a peer-reviewed journal. The condensed consolidated financial statements do not include any adjustments that might result from the outcome of this uncertainty. These condensed consolidated financial statements have been prepared under the assumption of a going concern, which assumes that the Company will be able to realize its assets and discharge its liabilities in the normal course of business. The Company's ability to continue its operations is dependent upon obtaining new financing for its ongoing operations. Future financing options available to the Company include equity financings and loans and if the Company is unable to obtain such additional financing timely, or on favorable terms, the Company may have to curtail its development, marketing and promotional activities, which would have a material adverse effect on its business, financial condition and results of operations, and it could ultimately be forced to discontinue its operations and liquidate. These matters raise substantial doubt about the Company's ability to continue as a going concern for a reasonable period of time, which is defined as within one year after the date that the condensed consolidated financial statements are issued. Realization of the Company's assets may be substantially different from the carrying amounts presented in these condensed consolidated financial statements and the accompanying condensed consolidated financial statements do not include any adjustments that may become necessary, should the Company be unable to continue as a going concern.
NOTE 3 - SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES
Significant Accounting Policies
There have been no material changes to the Company's significant accounting policies as set forth in the Company's audited consolidated financial statements included in the Annual Report on Form 10-K for the year endedDecember 31, 2021 under Note 3 - Summary of Significant Accounting Policies, except as disclosed in this note. Basis of Presentation The accompanying unaudited condensed consolidated financial statements of the Company have been prepared on a going concern basis in accordance with accounting principles generally accepted inthe United States of America (GAAP) for interim financial reporting and as required by Regulation S-X, Rule 10-01. Accordingly, they do not include all of the information and footnotes required by GAAP for complete financial statements. In the opinion of management, all adjustments (including those which are normal and recurring) considered necessary for a fair presentation of the interim financial information have been included. When preparing financial statements in conformity with GAAP, the Company must make estimates and assumptions that affect the reported amounts of assets, liabilities, revenues, expenses and related disclosures at the date of the financial statements. Actual results could differ from those estimates. Additionally, operating results for the three months endedMarch 31, 2022 , are not necessarily indicative of the results that may be expected for any other interim period or for the fiscal year endingDecember 31, 2021 . For further information, refer to the financial statements and footnotes included in the Company's annual financial statements for the fiscal year endedDecember 31, 2020 , which are included in the Company's annual report on Form 10-K filed with theSEC onMarch 30, 2022 . Use of Estimates The preparation of financial statements in conformity withU.S. GAAP requires management to make estimates, judgments, and assumptions that affect the reported amounts of assets, liabilities, revenues and expenses, together with amounts disclosed in the related notes to the condensed consolidated financial statements. The Company's significant estimates and assumptions used in these financial statements include, but are not limited to, the fair value of financial instruments warrants, options and equity shares; the valuation of stock-based compensation; and the estimates and assumptions related to impairment analysis of goodwill and other intangible assets. Certain of the Company's estimates could be affected by external conditions, including those unique to the Company and general economic conditions. It is reasonably possible that these external factors could have an effect on the Company's estimates and may cause actual results to differ from those estimates. 7 Foreign Currency Translation The Company's reporting currency isthe United States dollar. The functional currency of certain subsidiaries is the Canadian Dollar ("CAD") (0.7613 and0.7874 CAD to1 US dollar each as ofMarch 31, 2022 andDecember 31, 2021 , respectively) or British Pound ("GBP") (1.3133 and1.3510 GBP to1 US dollar , each as ofMarch 31, 2022 andDecember 31, 2021 , respectively), while expense accounts are translated at the weighted average exchange rate for the period (0.7454 and0.7896 CAD to1 US dollar and 1.3413 and1.3784 GBP to1 US dollar for each of the three months endedMarch 31, 2022 and 2021, respectively). Equity accounts are translated at historical exchange rates. The resulting translation adjustments are recognized in stockholders' equity as a component of accumulated other comprehensive income. Comprehensive income (loss) is defined as the change in equity of an entity from all sources other than investments by owners or distributions to owners and includes foreign currency translation adjustments as described above. During the three months endedMarch 31, 2022 and 2021, the Company recorded other comprehensive (loss) income of ($728,081 ) and$189,348 , respectively, as a result of foreign currency translation adjustments. Foreign currency gains and losses resulting from transactions denominated in foreign currencies, including intercompany transactions, are included in results of operations. The Company recognized ($142 ) and$11,148 of foreign currency transaction (losses) gains for the three months endedMarch 31, 2022 and 2021, respectively. Such amounts have been classified within general and administrative expenses in the accompanying condensed consolidated statements of operations and comprehensive income (loss). Accrued Issuable Equity The Company records accrued issuable equity when it is contractually obligated to issue shares and sometimes there are administrative delays in the issuance of such shares. Accrued issuable equity is recorded and carried at fair value with changes in its fair value recognized in the Company's condensed consolidated statement of operations. Once the underlying shares of common stock are issued, the accrued issuable equity is reclassified as of the share issuance date at the then current fair market value of the common stock.
Net Income (Loss) Per Common Share
Basic net income (loss) per common share is computed by dividing net income (loss) by the weighted average number of common shares outstanding during the period. Diluted net income (loss) per common share is computed by dividing net income (loss) by the weighted average number of common shares outstanding, plus the number of additional common shares that would have been outstanding if the common share equivalents had been issued (computed using the treasury stock or if converted method), if dilutive. The following table details the net income (loss) per share calculation, reconciles between basic and diluted weighted average shares outstanding, and presents the potentially dilutive shares that are excluded from the calculation of the weighted average diluted common shares outstanding, because their inclusion would have been anti-dilutive: For the Three Months Ended March 31, 2022 2021 Numerator: Net income (loss)$ 1,563,713 $ (16,198,585 )
Weighted average shares outstanding (denominator for basic earnings per share)
34,059,927 27,953,302
Effects of dilutive securities: Assumed exercise of stock options, treasury stock method 8,834 - Assumed exercise of warrants, treasury stock method - - Dilutive potential common shares 8,834 - Weighted average shares and assumed potential common shares (denominator for diluted earnings per share, treasury method) 34,068,762 27,953,302 Basic earnings per share$ 0.05 $ (0.58 ) Diluted earnings per share$ 0.05 $ (0.58 ) 8 The following common share equivalents are excluded from the calculation of weighted average common shares outstanding, because their inclusion would have been anti-dilutive: For the Three Months Ended March 31, 2022 2021 Options 2,691,000 1,630,000 Warrants 11,153,908 8,628,908 Convertible debt (a) - 100,361
Total potentially dilutive shares 13,844,908 10,359,269
a) Represents shares issuable upon conversion of debt at various conversion
prices, some of which were calculated using the fair value of the Company's
common stock at the respective balance sheet date.
Warrant, Option and Convertible Instrument Valuation
The Company has computed the fair value of warrants and options using a Black-Scholes model. The expected term used for warrants is the contractual life and the expected term used for options issued is the estimated period of time that options granted are expected to be outstanding. The Company utilizes the "simplified" method to develop an estimate of the expected term of "plain vanilla" option grants. The Company is utilizing an expected volatility figure based on a review of the historical volatilities, over a period of time, equivalent to the expected life of the instrument being valued, of similarly positioned public companies within its industry. The risk-free interest rate was determined from the implied yields fromU.S. Treasury zero-coupon bonds with a remaining term consistent with the expected term of the instrument being valued. Subsequent Events
The Company has evaluated events that have occurred after the balance sheet date but before these condensed consolidated financial statements were issued. Based upon that evaluation, the Company did not identify any recognized or non-recognized subsequent events that would have required adjustment or disclosure in the financial statements, except as disclosed in Note 11 - Subsequent Events.
Recently Issued Accounting Pronouncements
Management does not believe that any recently issued, but not yet effective, accounting pronouncements, if currently adopted, would have a material effect on the Company's unaudited condensed consolidated financial statements. 9 NOTE 4 - ACCRUED EXPENSES Accrued expenses consist of the following as ofMarch 31, 2022 andDecember 31, 2021 : March 31, December 31, 2022 2021 Consulting fees$ 427,197 $ 548,281 Professional fees 195,765 252,973 Litigation settlements (1) 1,025,122 300,000 Employee and director compensation 786,721 725,569 Research and development fees 159,694 91,737 Interest 28,067 25,433 Other 4,895 20,587$ 2,627,461 $ 1,964,580
(1) See Note 8 - Commitments and Contingencies, Legal Matters.
As of
NOTE 5 - ACCRUED ISSUABLE EQUITY
The Company entered into five separate agreements with consultants who are members of theScientific Advisory Board ("SAB") and will provide for services and duties which will be requested by the Company's Chief Scientific Officer from time to time. The agreements, which have a term of two years, provide for the issuance of 2,400 share of common stock to each consultant annually, with each grant vesting monthly over twenty-four months. As ofMarch 31, 2022 , these shares have yet to be issued. The shares were recorded as a liability on the balance sheet at a market price of$4.05 per share for an aggregate value of$48,600 ; upon assessment of fair value of$2.59 per share atMarch 31, 2022 , the Company recorded a change in fair market value of$17,520 . A summary of the accrued issuable equity activity during the three months endedMarch 31, 2022 is presented below: Balance at January 1, 2022 $ - Additions 48,600 Mark to market (17,520 )
Balance at
10
NOTE 6 - DERIVATIVE LIABILITIES
The following table sets forth a summary of the changes in the fair value of Level 3 derivative liabilities (except the Public SPAC warrants as defined below, which are Level 1 derivative liabilities) that are measured at fair value on a recurring basis: Warrants Public Private SPAC SPAC PIPE Other Total Balance as of January 1, 2022$ 8,048,850 $ 467,325 $ 6,516,300 $ 187,892 $ 15,220,367 Change in fair value of derivative liabilities (1,852,650 ) (251,250 )
(3,044,800 ) (81,414 ) (5,230,114 )
Balance as of
The fair value of the derivative liabilities as ofMarch 31, 2022 andDecember 31, 2021 were estimated using the Black Scholes option pricing model, with the following assumptions used:March 31, 2022 Risk-free interest rate 2.30% - 2.44% Expected term in years 2.34 - 3.90 Expected volatility 91.0% - 105% Expected dividends 0%December 31, 2021 Risk-free interest rate 0.85% - 1.14% Expected term in years 2.59 - 4.15 Expected volatility 98.5% Expected dividends 0% SPAC Warrants Public SPAC Warrants Participants in KBL's initial public offering received an aggregate of 11,500,000 warrants ("Public SPAC Warrants"). Each Public SPAC Warrant entitles the holder to purchase one-half of one share of the Company's common stock at an exercise price of$5.75 per half share ($11.50 per whole share) untilNovember 6, 2025 , subject to adjustment. No fractional shares will be issued upon exercise of the Public SPAC Warrants. Management has determined that the Public SPAC Warrants contain a tender offer provision which could result in the Public SPAC Warrants settling for the tender offer consideration (including potentially cash) in a transaction that didn't result in a change-in-control. This feature results in the Public SPAC Warrants being precluded from equity classification. Accordingly, the Public SPAC Warrants are classified as liabilities measured at fair value, with changes in fair value each period reported in earnings. The Public SPAC Warrants were revalued onMarch 31, 2022 at$6,196,200 , which resulted in a$1,852,650 decrease in the fair value of the derivative liabilities during the three months endedMarch 31, 2022 . 11 Private SPAC Warrants Participants in KBL's initial private placement in connection with its initial public offering received an aggregate of 502,500 warrants ("Private SPAC Warrants"). Each Private SPAC Warrant entitles the holder to purchase one-half of one share of the Company's common stock at an exercise price of$5.75 per half share ($11.50 per whole share) untilNovember 6, 2025 , subject to adjustment. No fractional shares will be issued upon exercise of the Private SPAC Warrants. Management has determined that the Private SPAC Warrants contain a tender offer provision which could result in the Private SPAC Warrants settling for the tender offer consideration (including potentially cash) in a transaction that didn't result in a change-in-control. This feature (amongst others) results in the Private SPAC Warrants being precluded from equity classification. Accordingly, the Private SPAC Warrants are classified as liabilities measured at fair value, with changes in fair value each period reported in earnings. The Private SPAC Warrants were revalued onMarch 31, 2022 at$216,075 , which resulted in a$251,250 decrease in the fair value of the derivative liabilities during the three months endedMarch 31, 2022 . PIPE Warrants OnFebruary 23, 2021 , the Company issued five-year warrants (the "PIPE Warrants") to purchase 2,564,000 shares of common stock at an exercise price of$5.00 per share in connection with a private placement offering. The PIPE Warrants did not meet the requirements for equity classification due to the existence of a tender offer provision that could potentially result in cash settlement of the PIPE Warrants that didn't meet the limited exception in the case of a change-in-control. Accordingly, the PIPE Warrants are liability-classified and the Company recorded the$7,294,836 fair value of the PIPE Warrants, which was determined using the Black-Scholes option pricing model, as derivative liabilities. The PIPE Warrants were revalued onMarch 31, 2022 at$3,471,500 , which resulted in a$3,044,800 decrease in the fair value of the derivative liabilities during the three months endedMarch 31, 2022 . Other Warrants AGP Warrant
In connection with the transactions contemplated by the Company's Business Combination Agreement (as amended, the "Business Combination Agreement"), dated as ofJuly 25, 2019 (the "Business Combination"), onNovember 6, 2020 , the Company became obligated to assume five-year warrants for the purchase of 63,658 shares of the Company's common stock at an exercise price of$5.28 per share (the "AGP Warrant Liability") that had originally been issued by KBL to an investment banking firm in connection with a prior private placement. OnMarch 12, 2021 , the Company issued a warrant toAlliance Global Partners ("AGP" and the "AGP Warrant") to purchase up to an aggregate of 63,658 shares of the Company's common stock at a purchase price of$5.28 per share, subject to adjustment, in full satisfaction of the AGP Warrant Liability. The exercise of the AGP Warrant is limited at any given time to prevent AGP from exceeding beneficial ownership of 4.99% of the then total number of issued and outstanding shares of the Company's common stock upon such exercise. The warrant is exercisable at any time betweenMay 2, 2021 andMay 2, 2025 . The AGP Warrant did not meet the requirements for equity classification due to the existence of a tender offer provision that could potentially result in cash settlement of the AGP Warrant that did not meet the limited exception in the case of a change-in-control. Accordingly, the AGP Warrant will continue to be liability-classified. The AGP Warrant was revalued onMarch 31, 2022 at$86,447 , which resulted in a$57,884 decrease in the fair value of the derivative liabilities during the three months endedMarch 31, 2022 . 12 Alpha Warrant In connection with that certain Mutual Release and Settlement Agreement datedJuly 31, 2021 (agreed to onJuly 29, 2021 ) between the Company andAlpha Capital Anstal ("Alpha" and the "Alpha Settlement Agreement"), the Company issued a three-year warrant for the purchase of 25,000 shares of the Company's common stock at an exercise price of$7.07 per share (the "Alpha Warrant Liability" and the "Alpha Warrant"). The exercise of shares of the Alpha Warrant is limited at any given time to prevent Alpha from exceeding a beneficial ownership of 4.99% of the then total number of issued and outstanding shares of the Company's common stock upon such exercise. The warrant is exercisable untilAugust 2, 2024 . The Alpha Warrant did not meet the requirements for equity classification due to the existence of a tender offer provision that could potentially result in cash settlement of the Alpha Warrant that did not meet the limited exception in the case of a change-in-control. Accordingly, the Alpha Warrant is liability-classified and the Company recorded the$95,677 fair value of the Alpha Warrant, which was determined using the Black-Scholes option pricing model, as a derivative liability. The Alpha Warrant was revalued onMarch 31, 2022 at$20,031 , which resulted in a$23,530 decrease in the fair value of the derivative liabilities during the three months endedMarch 31, 2022 . The following assumptions were used to value the Alpha Warrant at issuance: Warrant Activity A summary of the warrant activity (including theAugust 2021 PIPE Warrants, which are equity-classified) during the three months endedMarch 31, 2022 is presented below: Weighted Average Weighted Remaining Number of Average Life in Intrinsic Warrants Exercise Price Years Value Outstanding, December 31, 2021 11,153,908 9.06 4.1 Issued - - Exercised - - Cancelled - - Expired - - Outstanding, March 31, 2022 11,153,908 $ 9.06 3.8 - Exercisable, March 31, 2022 11,153,908 $ 9.06 3.8 - A summary of outstanding and exercisable warrants as ofMarch 31, 2022 is presented below: Warrants Outstanding Warrants Exercisable Weighted Average Exercise Number of Remaining Number of Price Shares Life in Years Shares$ 5.00 2,564,000 3.9 2,564,000$ 5.28 63,658 3.1 63,658$ 7.07 25,000 2.3 25,000$ 7.50 2,500,000 4.4 2,500,000$ 11.50 6,001,250 3.6 6,001,250 11,153,908 3.8 11,153,908 13 NOTE 7 - LOANS PAYABLE Loans Payable
The following table summarizes the activity of loans payable during the three
months ended
Principal Effect of Principal Balance at Principal Foreign Balance at December 31, Repaid in Exchange March 31, 2021 Forgiveness Cash Adjustment Rates 2022 Paycheck Protection Program$ 41,312 $ - $ (30,967
) $ - $ -
61,169 - (3,131 ) - (1,710 ) 56,328 First Assurance Funding 1,618,443 - (481,321 ) (14,042 )(2) - 1,123,080 Other loans payable 155,320 - - (5,000 )(1) - 150,320 Total loans payable$ 1,876,244 $ -$ (515,419 ) $ (19,042 ) $ (1,710 ) $ 1,340,073 Less: loans payable - current portion 1,828,079 1,296,466 Loans payable - noncurrent portion$ 48,165 $ 43,607
(1) Note that this amount was reclassified to related party payables.
(2) Note that this amount was related to finance charges and was reclassified.
During the three months endedMarch 31, 2022 , the Company paid an aggregate of$481,321 ,$3,131 and$30,967 in partial satisfaction of the First Assurance Funding loan, the Bounce Back Loan Scheme and the Paycheck Protection Program loan, respectively.
Loans Payable - Related Parties
The below table summarizes the activities of loans payable - related parties
during the three months ended
Principal Effect of Principal Balance at Reclass Foreign Balance at December 31, from Loans Exchange March 31, 2021 Payable Rates 2022
Loans payable issued between
Interest Expense on Loans Payable
For the three months ended
As ofMarch 31, 2022 , the Company had accrued interest and accrued interest - related parties associated with loans of$27,086 and$12,818 , respectively. As ofDecember 31, 2021 , the Company had accrued interest and accrued interest - related parties associated with loans of$24,212 and$812 , respectively. See Note 10 - Related Parties for additional details. 14
NOTE 8 - COMMITMENTS AND CONTINGENCIES
Litigation and Other Loss Contingencies
The Company records liabilities for loss contingencies arising from claims, assessments, litigation, fines, penalties and other sources when it is probable that a liability has been incurred and the amount of the loss can be reasonably estimated. The Company has no liabilities recorded for loss contingencies as ofDecember 31, 2021 . See Legal Matters - Action Against Former Executive of KBL below for information related to aMarch 31, 2022 accrual. Legal Matters
Action Against Former Executive of KBL
OnSeptember 1, 2021 , the Company initiated legal action in theChancery Court of Delaware against Dr.Marlene Krauss ("Dr. Krauss") and two of her affiliated companies,KBL IV Sponsor, LLC andKBL Healthcare Management, Inc. (collectively, the "KBL Affiliates") for, among other things, engaging in monetary transfers of the Company's assets, non-disclosure of financial liabilities in the Company's Consolidated Financial Statements, issuing shares of stock without authorization; and allowing stockholder redemptions to take place. The Company's complaint alleges causes of action againstDr. Krauss and/or the KBL Affiliates for breach of fiduciary duties, ultra vires acts, unjust enrichment, negligence and declaratory relief, and seeks compensatory damages in excess of$11,286,570 , together with interest, attorneys' fees and costs. There can be no assurance that the Company will be successful in its legal actions. As ofDecember 31, 2021 , the Company recorded a legal accrual of$250,000 to cover the legal expenses of the former executives of KBL. OnOctober 5, 2021 ,Dr. Krauss and the KBL Affiliates filed an Answer, Counterclaims and Third-Party Complaint (the "Krauss Counterclaims") against the Company and twelve individuals who are, or were, directors and/or officers of the Company, i.e.,Marc Feldmann ,Lawrence Steinman ,James N. Woody ,Teresa DeLuca , Frank Knuettel II,Pamela Marrone ,Lawrence Gold ,Donald A. McGovern , Jr., Russell T. Ray,Richard W. Barker ,Shoshana Shendelman andOzan Pamir (collectively, the "Third-Party Defendants"). OnOctober 27, 2021 , the Company andOzan Pamir filed an Answer to the Krauss Counterclaims, and all of the other Third-Party Defendants filed a Motion to Dismiss as to the Third-Party Complaint. OnJanuary 28, 2022 , in lieu of filing an opposition to the Motion to Dismiss,Dr. Krauss and the KBL Affiliates filed a Motion for leave to file amended counterclaims and third-party complaint, and to dismiss six of the current and former directors previously named, i.e., to dismissTeresa DeLuca , Frank Knuettel II,Pamela Marrone , Russell T. Ray,Richard W. Barker andShoshana Shendelman . The Motion was granted by stipulation and, onFebruary 24, 2022 ,Dr. Krauss filed an amended Answer, Counterclaims and Third-Party Complaint (the "Amended Counterclaims"). In essence, the Amended Counterclaims allege (a) that the Company and the remaining Third-Party Defendants breached fiduciary duties toDr. Krauss by making alleged misstatements againstDr. Krauss inSEC filings and failing to register her shares in the Company so that they could be traded, and (b) the Company breached contracts between the Company andDr. Krauss for registration of such shares, and also failed to pay toDr. Krauss the amounts alleged to be owing under a promissory note in the principal amount of$371,178 , plus an additional$300,000 underDr. Krauss's resignation agreement. The Amended Counterclaims seek unspecified amounts of monetary damages, declaratory relief, equitable and injunctive relief, and attorney's fees and costs. OnMarch 16, 2022 ,Donald A. McGovern , Jr. andLawrence Gold filed a Motion to Dismiss the Amended Counterclaims against them, and the Company and the remaining Third-Party Defendants filed an Answer to the Amended Counterclaims denying the same. The Company and the Third-Party Defendants intend to continue to vigorously defend against all of the Amended Counterclaims, however, there can be no assurance that they will be successful in the legal defense of such Amended Counterclaims. InApril 2022 ,Donald A. McGovern , Jr. andLawrence Gold were removed from the lawsuit as parties. Discovery has not yet commenced in the case. 15
Action Against the Company by
OnAugust 19, 2021 ,Dr. Krauss initiated legal action in theChancery Court of Delaware against the Company. The original Complaint sought expedited relief and made the following two claims: (1) it alleged that the Company is obligated to advance expenses including, attorney's fees, toDr. Krauss for the costs of defending against theSEC and certain Subpoenas served by theSEC onDr. Krauss ; and (2) it alleged that the Company is also required to reimburseDr. Krauss for the costs of bringing this lawsuit against the Company. On or aboutSeptember 3, 2021 ,Dr. Krauss filed an Amended and Supplemental Complaint (the "Amended Complaint") in this action, which added the further claims thatDr. Krauss is also allegedly entitled to advancement by the Company of her expenses, including attorney's fees, for the costs of defending against the Third-Party Complaint in the Tyche action referenced below, and the costs of defending against the Company's own Complaint againstDr. Krauss as described above. On or aboutSeptember 23, 2021 , the Company filed its Answer to the Amended Complaint in which the Company denied each ofDr. Krauss' claims and further raised numerous affirmative defenses with respect thereto. OnNovember 15, 2021 ,Dr. Krauss filed a Motion for Summary Adjudication as to certain of the issues in the case, which was opposed by the Company. A hearing on such Motion was held onDecember 7, 2021 , and, onMarch 7, 2022 , the Court issued a decision in the matter denying the Motion for Summary Adjudication in part and granting it in part. The Court then issued an Order implementing such a decision onMarch 29, 2022 . The parties are now engaging in proceedings set forth in that implementing Order. The Court grantedDr. Krauss's request for advancement of certain legal fees and the Company was required to pay a portion of those fees while it objects to the remaining portion of the fees. These legal fees have been accrued on the Company's balance sheet as ofMarch 31, 2022 (see Note 11 - Subsequent Events for more details). Notwithstanding any requirement by the Court for the Company to advance attorneys' fees toDr. Krauss , no adjudication has yet been made as to whetherDr. Krauss will ultimately be entitled to permanently retain such advancements. The Company is seeking payment for a substantial portion of such amounts from its director and officers' insurance policy, of which no assurance can be provided that the directors and officers insurance policy will cover such amounts.
The Company commenced and filed an action against defendantTyche Capital LLC ("Tyche") in theSupreme Court of New York , in the County ofNew York , onApril 15, 2021 . In its Complaint, the Company alleged claims against Tyche arising out of Tyche's breach of its written contractual obligations to the Company as set forth in a "Guarantee And Commitment Agreement" datedJuly 25, 2019 , and a "Term Sheet For KBL Business Combination With CannBioRex" datedApril 10, 2019 (collectively, the "Subject Guarantee"). The Company alleges in its Complaint that, notwithstanding demand having been made on Tyche to perform its obligations under the Subject Guarantee, Tyche has failed and refused to do so, and is currently in debt to the Company for such failure in the amount of$6,776,686 , together with interest accruing thereon at the rate set forth in the Subject Guarantee. On or aboutMay 17, 2021 , Tyche responded to the Company's Complaint by filing an Answer and Counterclaims against the Company alleging that it was the Company, rather than Tyche, that had breached the Subject Guarantee. Tyche also filed a Third-Party Complaint against six third-party defendants, including three members of the Company's management, SirMarc Feldmann , Dr.James Woody , andOzan Pamir (collectively, the "Individual Company Defendants"), claiming that they allegedly breached fiduciary duties to Tyche with regards to the Subject Guarantee. In that regard, onJune 25, 2021 , each of the Individual Company Defendants filed a Motion to Dismiss Tyche's Third-Party Complaint against them. OnNovember 23, 2021 , the Court granted the Company's request to issue an Order of attachment against all of Tyche's shares of the Company's stock that had been held in escrow. In so doing, the Court found that the Company had demonstrated a likelihood of success on the merits of the case based on the facts alleged in the Company's Complaint. OnFebruary 18, 2022 , Tyche filed an Amended Answer, Counterclaims and Third-Party Complaint. OnMarch 22, 2022 , the Company and each of the Individual Company Defendants filed a Motion to Dismiss all of Tyche's claims. A hearing on such Motion to Dismiss is scheduled by the Court forAugust 17, 2022 . The Company and the Individual Company Defendants intend to continue to vigorously defend against all of Tyche's claims, however, there can be no assurance that they will be successful in the legal defense of such claims. Written discovery proceedings have commenced among the parties. 16
Action Against
The Company and two of its wholly-owned subsidiaries,Katexco Pharmaceuticals Corp. andCannBioRex Pharmaceuticals Corp. (collectively, the "Company Plaintiffs"), initiated legal action againstRonald Bauer andSamantha Bauer , as well as two of their companies,Theseus Capital Ltd. andAstatine Capital Ltd. (collectively, the "Bauer Defendants"), in theSupreme Court of British Columbia onFebruary 25, 2022 . The Company Plaintiffs are seeking damages against the Bauer Defendants for misappropriated funds and stock shares, unauthorized stock sales, and improper travel expenses, in the combined sum of at least$4,395,000 CAD [$3,460,584 USD ] plus the additional sum of$2,721,036 USD . Service of process has been effected on each of the Bauer Defendants, and the Bauer Defendants filed an answer onMay 6, 2022 . There can be no assurance that the Company Plaintiffs will be successful in this legal action. NOTE 9 - STOCKHOLDERS' EQUITY Common Stock
Common Stock Issued for Services
During the three months endedMarch 31, 2022 , the Company issued an aggregate of 51,319 immediately vested shares of the Company's common stock as compensation to consultants, directors, and officers, with an aggregate issuance date fair value of$149,718 , which was charged immediately to the condensed consolidated statement of operations for the three months endedMarch 31, 2022 . Stock Options A summary of the option activity during the three months endedMarch 31, 2022 is presented below: Weighted Weighted Average Average Number of Exercise Remaining Intrinsic Options Price Term (Yrs) Value Outstanding, January 1, 2022 2,741,000 4.77 9.4 70,500 Granted - - Exercised - - Expired - - Forfeited - - Outstanding, March 31, 2022 2,741,000 4.77 9.2$ 5,000 Exercisable, March 31, 2022 1,105,528 4.46 9.1$ 5,000 As indicated in the table above, no options were issued for the three months endedMarch 31, 2022 . For options issued during the three months endedMarch 31, 2021 , the assumptions used in the Black Scholes valuation method were as follows: For the Three Months Ended March 31, 2022
Risk-free interest rate 0.75% Expected term in years 5.27 - 5.38 Expected volatility 100% Expected dividends 0% A summary of outstanding and exercisable stock options as ofMarch 31, 2022 is presented below: Stock Options Outstanding Stock Options Exercisable Weighted Average Exercise Number of Remaining Number of Price Shares Life in Years Shares$ 2.49 50,000 8.7 50,000$ 4.43 1,580,000 8.9 772,444$ 7.56 436,000 9.3 72,667$ 3.95 675,000 9.7 210,417 2,741,000 9.1 1,105,528 17
The Company recognized stock-based compensation expense of$596,467 for the three months endedMarch 31, 2022 , related to the amortization of stock options. Expense of$514,696 is included within general and administrative expenses and expense of$81,771 is included within research and development expenses on the condensed consolidated statements of operations. The full amount of stock-based compensation recognized for the period endedMarch 31, 2022 is considered to be related party expense. Stock-based compensation expense for the three months endedMarch 31, 2021 was$1,092,399 ; these expenses were included within general and administrative expenses on the condensed consolidated statement of operations for that period. The full amount of stock-based compensation recognized for the period endedMarch 31, 2021 was considered to be related party expense. As ofMarch 31, 2022 , there was$5,705,889 of unrecognized stock-based compensation expense that will be recognized over the weighted average remaining vesting period of 2.81 years. NOTE 10 - RELATED PARTIES
Accrued Expenses - Related Parties
Accrued expenses - related parties was$37,640 as ofMarch 31, 2022 and consists of$12,818 of interest accrued on loans due to a certain investor in the Company and$24,820 of accrued consulting fees for services provided by certain directors of the Company. Accrued expenses - related parties of$18,370 as ofDecember 31, 2021 , consists of interest accrued on loans and convertible notes due to certain officers and directors of the Company.
Loans Payable - Related Parties
Loans payable - related parties consists of$86,034 and$81,277 as ofMarch 31, 2022 andDecember 31, 2021 , respectively. See Note 7 - Loans Payable for more information.
Research and Development Expenses - Related Parties
Research and Development Expenses - Related Parties were$47,718 and$267,053 during the three months endedMarch 31, 2022 and 2021, respectively, and are related to consulting and professional fees paid to current or former officers, directors or greater than 5% stockholders, or affiliates thereof.
General and Administrative Expenses - Related Parties
General and Administrative Expenses - Related Parties during the three months
ended
Interest Expense - Related Parties
During the three months ended
During the three months endedMarch 31, 2021 , the Company recorded$13,949 of interest expense - related parties, of which$11,526 related to interest on certain convertible notes held by officers and directors of the Company and$2,423 related to interest expense on loans from officers, directors greater than 5% stockholders, or affiliates thereof, of the Company. 18 NOTE 11 - SUBSEQUENT EVENTS
Amendments to Employee Agreements
As disclosed in the Company's previous filings, onApril 27, 2022 , the Company entered into amendments with six of its officers, executives and a consultant to revise the compensation agreements currently in place with such individuals. The agreements for three officers were amended to increase their base salaries by 3% and then, effectiveMarch 1, 2022 , the base salaries of two of the officers were reduced by 20% each and the other salary was reduced by 25%; such reduced amounts (the "Accrued Amounts") will be accrued until such time as the Company has sufficient cash on hand to pay the Accrued Amounts, which the Company expects will not be until it has raised a minimum of$15,000,000 (the "Funding Determination Date"). On the Funding Determination Date, their salaries will increase to the full new base salary and the Accrued Amounts will be paid by the Company, provided that in addition, at the discretion of the Board of Directors, the base salaries on the Funding Determination Date of each executive may be further increased by 2%.
Pursuant to the amendments for two executives' agreements, effectiveMarch 1, 2022 , each of their salaries were reduced by$225,000 (100%) and$56,250 (25%), respectively, and such reduced amounts will be accrued and paid on the Funding Determination Date.
In addition, pursuant to the consultant's agreement, upon acceptance of the data for the Phase 2b clinical trial for Dupuytren's Contracture for publication, which has occurred, his monthly fee increased to £23,000, provided that £4,000 of such increase will be accrued and £19,000 of such fees will be payable monthly per the payroll practices of the Company in cash effectiveMarch 1, 2022 and until the earlier of (a)November 1, 2022 or (b) the Funding Determination Date, at which time all Accrued Amounts will be due.
Legal Matter - Action against the Company by
OnApril 29, 2022 , pursuant to the legal matter described in Note 8 - "Legal Matters - Action Against the Company byDr. Krauss ", the Company paid$975,121 for advancement of legal fees incurred byDr. Krauss , pursuant to a court order. The payment was made to an escrow account and the Company has objected to the amounts and nature of the expenses. Furthermore, the Company has filed a reimbursement claim for the amount advanced net of its deductible of$250,000 with its director and officers' insurance policy carrier, of which no assurance can be provided that the directors and officers' insurance policy will cover such amounts. 19
ITEM 2. Management's Discussion and Analysis of Financial Condition and Results of Operations
CAUTIONARY NOTE REGARDING FORWARD-LOOKING STATEMENTS This Quarterly Report on Form 10-Q ("Report"), including "Management's Discussion and Analysis of Financial Condition and Results of Operations," set forth below, contains forward-looking statements, within the federal securities laws, including the Private Securities Litigation Reform Act of 1995, regarding future events and the future results of the Company that are based on current expectations, estimates, forecasts, and projections about the industry in which the Company operates and the beliefs and assumptions of the management of the Company. Words such as "expects," "anticipates," "targets," "goals," "projects," "intends," "plans," "believes," "seeks," "estimates," variations of such words, and similar expressions are intended to identify such forward-looking statements. These forward-looking statements are only predictions and are subject to risks, uncertainties and assumptions that are difficult to predict. Therefore, actual results may differ materially and adversely from those expressed in any forward-looking statements. Factors that might cause or contribute to such differences include, but are not limited to, those discussed elsewhere in this Report, including under "Risk Factors", and in other reports the Company files with theSecurities and Exchange Commission ("SEC"), including the Company's Annual Report on Form 10-K for the year endedDecember 31, 2021 , as filed with theSEC onMarch 31, 2022 (under the heading "Risk Factors" and in other parts of that report), and include, but are not limited to, statements about:
? Expectations for the clinical and preclinical development, manufacturing,
regulatory approval, and commercialization of our product candidates; ? regulatory developments inthe United States and foreign countries; ? our success in retaining or recruiting, or changes required in, our officers, key employees or directors;
? current negative operating cash flows and our potential ability to obtain
additional financing to advance our business and the terms of any further
financing, which may be highly dilutive and may include onerous terms;
? the continued impact of the COVID-19 pandemic on our business operations
and our research and development initiatives; ? the accuracy of our estimates regarding expenses, future revenues and capital requirements;
? estimates of the sufficiency of our existing capital resources combined
with future anticipated cash flows to finance our operating requirements;
? our ability to maintain our listing on Nasdaq; and
? other risks and uncertainties, including those listed under "Risk Factors",
below.
All forward-looking statements speak only at the date of the filing of this Report. The reader should not place undue reliance on these forward-looking statements. Although we believe that our plans, intentions and expectations reflected in or suggested by the forward-looking statements we make in this Report are reasonable, we provide no assurance that these plans, intentions or expectations will be achieved. We disclose important factors that could cause our actual results to differ materially from our expectations under "Risk Factors" and "Management's Discussion and Analysis of Financial Condition and Results of Operations" and elsewhere in this Report and our Annual Report on Form 10-K for the year endedDecember 31, 2021 . These cautionary statements qualify all forward-looking statements attributable to us or persons acting on our behalf. Except as required by law, we assume no obligation to update or revise these forward-looking statements for any reason, even if new information becomes available in the future. 20 General Information
The following discussion is based upon our unaudited Condensed Consolidated Financial Statements included elsewhere in this Report, which have been prepared in accordance withU.S. generally accepted accounting principles. The preparation of these financial statements requires us to make estimates and judgments that affect the reported amounts of assets, liabilities, revenues and expenses, and related disclosure of contingencies. We base our estimates on historical experience and on various other assumptions that we believe to be reasonable under the circumstances, the results of which form the basis for making judgments about the carrying values of assets and liabilities that are not readily apparent from other sources. Actual results may differ from these estimates under different assumptions or conditions. Factors that could cause or contribute to these differences include those discussed below and elsewhere in this Report, and in other reports we file with theSEC , and in our most recent Annual Report on Form 10-K. All references to years relate to the calendar year endedDecember 31st of the particular year. This information should be read in conjunction with the interim unaudited condensed consolidated financial statements and the notes thereto included in this Quarterly Report on Form 10-Q, and the audited financial statements and notes thereto and "Part II. Other Information - Item 7. Management's Discussion and Analysis of Financial Condition and Results of Operations", contained in our Annual Report on Form 10-K for the year endedDecember 31, 2021 , filed with theSecurities and Exchange Commission onMarch 31, 2022 (the "Annual Report").
Certain capitalized terms used below and otherwise defined below, have the meanings given to such terms in the footnotes to our unaudited condensed consolidated financial statements included above under "Part I - Financial Information" - "Item 1. Financial Statements".
Please see the section entitled "Glossary" beginning on page ii of our Annual Report for a list of abbreviations and definitions commonly used in the pharmaceutical and biotechnology industry which are used throughout this Report.
Our logo and some of our trademarks and tradenames are used in this Report. This Report also includes trademarks, tradenames and service marks that are the property of others. Solely for convenience, trademarks, tradenames and service marks referred to in this Report may appear without the ®, ™ and SM symbols. References to our trademarks, tradenames and service marks are not intended to indicate in any way that we will not assert to the fullest extent under applicable law our rights or the rights of the applicable licensors if any, nor that respective owners to other intellectual property rights will not assert, to the fullest extent under applicable law, their rights thereto. We do not intend the use or display of other companies' trademarks and trade names to imply a relationship with, or endorsement or sponsorship of us by, any other companies. The market data and certain other statistical information used throughout this Report are based on independent industry publications, reports by market research firms or other independent sources that we believe to be reliable sources. Industry publications and third-party research, surveys and studies generally indicate that their information has been obtained from sources believed to be reliable, although they do not guarantee the accuracy or completeness of such information. We are responsible for all of the disclosures contained in this Report, and we believe these industry publications and third-party research, surveys and studies are reliable. While we are not aware of any misstatements regarding any third-party information presented in this Report, their estimates, in particular, as they relate to projections, involve numerous assumptions, are subject to risks and uncertainties, and are subject to change based on various factors, including those discussed under, and incorporated by reference in, the section entitled "Item 1A. Risk Factors" of this Report. These and other factors could cause our future performance to differ materially from our assumptions and estimates. Some market and other data included herein, as well as the data of competitors as they relate to the Company, is also based on our good faith estimates. See also "Cautionary Statement Regarding Forward-Looking Statements", above, which includes information on forward-looking statements used herein and other matters which are applicable to this Report, including, but not limited to this "Item 2. Management's Discussion and Analysis of Financial Condition and Results of Operations." 21 Unless the context requires otherwise, references to the "Company," "we," "us," "our," "180 Life", "180LS" and "180Life Sciences Corp. " refer specifically to180 Life Sciences Corp. and its consolidated subsidiaries. References to "KBL" refer to the Company prior to theNovember 6, 2020 Business Combination.
In addition, unless the context otherwise requires and for the purposes of this Report only:
"CAD" refers to Canadian dollars;
"Exchange Act" refers to the Securities Exchange Act of 1934, as amended;
"£" or "GBP" refers to British pounds sterling;
"SEC" or the "Commission" refers to the
"Securities Act" refers to the Securities Act of 1933, as amended.
Going Concern and Management Liquidity Plans
As ofMarch 31, 2022 , we had an accumulated deficit of$67,118,573 and net income for the three months endedMarch 31, 2022 of$1,563,713 . As ofMarch 31, 2022 , we had a working capital deficit of$6,120,408 . The accompanying condensed consolidated financial statements have been prepared assuming the Company will continue as a going concern. As we are not generating revenues, we need to raise a significant amount of capital in order to pay our debts and cover our operating costs. While the Company raised money inAugust 2021 , there is no assurance that we will be able to raise additional needed capital or that such capital will be available under favorable terms. We are subject to all the substantial risks inherent in the development of a new business enterprise within an extremely competitive industry. Due to the absence of a long-standing operating history and the emerging nature of the markets in which we compete, we anticipate operating losses until we can successfully implement our business strategy, which includes all associated revenue streams. We may never achieve profitable operations or generate significant revenues. We currently have a minimum monthly cash requirement spend of approximately$800,000 . We believe that in the aggregate, we will require significant additional capital funding to support and expand the research and development and marketing of our products, fund future clinical trials, repay debt obligations, provide capital expenditures for additional equipment and development costs, payment obligations, office space and systems for managing the business, and cover other operating costs until our planned revenue streams from products are fully-implemented and begin to offset our operating costs, if ever. Since our inception, we have funded our operations with the proceeds from equity and debt financings. We have experienced liquidity issues due to, among other reasons, our limited ability to raise adequate capital on acceptable terms. We have historically relied upon the issuance of equity and promissory notes that are convertible into shares of our common stock to fund our operations and have devoted significant efforts to reduce that exposure. We anticipate that we will need to issue equity to fund our operations and repay our outstanding debt for the foreseeable future. If we are unable to achieve operational profitability or we are not successful in securing other forms of financing, we will have to evaluate alternative actions to reduce our operating expenses and conserve cash. The accompanying condensed consolidated financial statements have been prepared in accordance with accounting principles generally accepted inthe United States of America on a going concern basis, which contemplates the realization of assets and the satisfaction of liabilities in the normal course of business. Accordingly, the consolidated financial statements do not include any adjustments relating to the recoverability of assets and classification of liabilities that might be necessary should the Company be unable to continue as a going concern. The consolidated financial statements included in this prospectus also include a going concern footnote. 22
Additionally, wherever possible, our Board of Directors will attempt to use non-cash consideration to satisfy obligations. In many instances, we believe that the non-cash consideration will consist of restricted shares of our common stock, preferred stock or warrants to purchase shares of our common stock. Our Board of Directors has authority, without action or vote of the shareholders, but subject to NASDAQ rules and regulations (which generally require shareholder approval for any transactions which would result in the issuance of more than 20% of our then outstanding shares of common stock or voting rights representing over 20% of our then outstanding shares of stock), to issue all or part of the authorized but unissued shares of common stock, preferred stock or warrants to purchase such shares of common stock. In addition, we may attempt to raise capital by selling shares of our common stock, possibly at a discount to market in the future. These actions will result in dilution of the ownership interests of existing shareholders, may further dilute common stock book value, and that dilution may be material. Such issuances may also serve to enhance existing management's ability to maintain control of us, because the shares may be issued to parties or entities committed to supporting existing management.Organization of MD&A
Our Management's Discussion and Analysis of Financial Condition and Results of Operations (the "MD&A") is provided in addition to the accompanying consolidated financial statements and notes to assist readers in understanding our results of operations, financial condition, and cash flows. MD&A is organized as follows: ? Business Overview and Recent Events. A summary of the Company's business and certain material recent events. ? Significant Financial Statement Components. A summary of the Company's significant financial statement components. ? Results of Operations. An analysis of our financial results comparing the three months endedMarch 31, 2022 and 2021. ? Liquidity and Capital Resources. An analysis of changes in our balance sheets and cash flows and discussion of our financial condition. ? Critical Accounting Policies and Estimates. Accounting estimates that we believe are important to understanding the assumptions and judgments incorporated in our reported financial results and forecasts.
Business Overview and Recent Events
OnNovember 6, 2020 ("Closing Date"), the Business Combination was consummated following a special meeting of stockholders, where the stockholders of KBL considered and approved, among other matters, a proposal to adopt the Business Combination Agreement. Pursuant to the Business Combination Agreement,KBL Merger Sub, Inc. merged with 180, with 180 continuing as the surviving entity and becoming a wholly-owned subsidiary of KBL. As part of the Business Combination, KBL issued 17,500,000 shares of common stock and equivalents to the stockholders of 180, in exchange for all of the outstanding capital stock of 180. The Business Combination became effectiveNovember 6, 2020 and in connection therewith, 180 filed a Certificate of Amendment of its Certificate of Incorporation inDelaware to change its name to 180 Life Corp., and KBL changed its name to180 Life Sciences Corp. Following the Closing of the Business Combination, we transitioned our operations to those of 180, which is a clinical stage biotechnology company headquartered inPalo Alto, California , focused on the development of therapeutics for unmet medical needs in chronic pain, inflammation, fibrosis and other inflammatory diseases, where anti-TNF therapy will provide a clear benefit to patients, by employing innovative research, and, where appropriate, combination therapy. We have three product development platforms: ? fibrosis and anti-tumor necrosis factor ("TNF"); ? drugs which are derivatives of cannabidiol ("CBD"); and ? alpha 7 nicotinic acetylcholine receptor ("?7nAChR"). 23 We have several future product candidates in development, including one product candidate which has recently completed a successful Phase 2b clinical trial in theUnited Kingdom for Dupuytren's Contracture, a condition that affects the development of fibrous connective tissue in the palm of the hand. 180 was founded by several world-leading scientists in the biotechnology and pharmaceutical sectors. We intend to invest resources to successfully complete the clinical programs that are underway, discover new drug candidates, and develop new molecules to build on our existing pipeline to address unmet clinical needs. The product candidates are designed via a platform comprised of defined unit operations and technologies. This work is performed in a research and development environment that evaluates and assesses variability in each step of the process in order to define the most reliable production conditions. We may rely on third-party contract manufacturing organizations ("CMOs") and other third parties for the manufacturing and processing of the product candidates in the future. We believe the use of contract manufacturing and testing for the first clinical product candidates is cost-effective and has allowed us to rapidly prepare for clinical trials in accordance with our development plans. We expect that third-party manufacturers will be capable of providing and processing sufficient quantities of these product candidates to meet anticipated clinical trial demands. COVID-19 Pandemic InDecember 2019 , a new strain of the coronavirus (COVID-19) was reported in Mainland China and during the first quarter of 2020 the virus had spread to over 150 countries, resulting in a global pandemic. This COVID-19 pandemic and the public health responses to contain it have resulted in global recessionary conditions, which did not exist atDecember 31, 2019 . Among other effects, government-mandated closures, stay-at-home orders and other related measures have significantly impacted global economic activity and business investment in general. A continuation or worsening of the levels of market disruption and volatility seen in the recent past could have an adverse effect on our ability to access capital, and on our business, results of operations and financial condition. We have been closely monitoring the developments and have taken active measures to protect the health of our employees, their families, and our communities. The ultimate impact on the 2022 fiscal year and beyond will depend heavily on the duration of the COVID-19 pandemic and public health responses, including government-mandated closures, stay-at-home orders and social distancing mandates, as well as the substance and pace of macroeconomic recovery, all of which are uncertain and difficult to predict considering the rapidly evolving landscape of the COVID-19 pandemic and the public health responses to contain it. The follow up time for patient data and the statistical analysis for the Phase 2b Dupuytren's Contracture clinical trial was delayed as a result of COVID-19, but such follow-up and statistical analysis are now completed and the Company announced the top-line data results from the Phase 2b trial onDecember 1, 2021 and the data was published onApril 29, 2022 in a peer-reviewed journal. Additionally, COVID-19 has delayed the initiation of certain clinical trials and may delay the initiation of other clinical trials in the future or otherwise have a material adverse effect on our future operations. 24
Significant Financial Statement Components
Research and Development
To date, 180's research and development expenses have related primarily to discovery efforts and preclinical and clinical development of its three product platforms: fibrosis and anti-TNF; drugs which are derivatives of CBD, and ?7nAChR. Research and development expenses consist primarily of costs associated with those three product platforms, which include:
? expenses incurred under agreements with 180's collaboration partners
and third-party contract organizations, investigative clinical
trial
sites that conduct research and development activities on its
behalf,
and consultants;
? costs related to production of clinical materials, including fees paid
to contract manufacturers;
? laboratory and vendor expenses related to the execution of preclinical
and clinical trials; ? employee-related expenses, which include salaries, benefits and stock-based compensation; and ? facilities and other expenses, which include expenses for rent and maintenance of facilities, depreciation and amortization expense and other supplies.
We expense all research and development costs in the periods in which they are incurred. We accrue for costs incurred as services are provided by monitoring the status of each project and the invoices received from our external service providers. We adjust our accrual as actual costs become known. When contingent milestone payments are owed to third parties under research and development arrangements or license agreements, the milestone payment obligations are expensed when the milestone results are achieved. Research and development activities are central to our business model. Product candidates in later stages of clinical development generally have higher development costs than those in earlier stages of clinical development, primarily due to the increased size and duration of later-stage clinical trials. We expect that research and development expenses will increase over the next several years as clinical programs progress and as we seek to initiate clinical trials of additional product candidates. It is also expected that increased research and development expenses will be incurred as additional product candidates are selectively identified and developed. However, it is difficult to determine with certainty the duration and completion costs of current or future preclinical programs and clinical trials of product candidates. The duration, costs and timing of clinical trials and development of product candidates will depend on a variety of factors that include, but are not limited to, the following: ? per patient trial costs; ? the number of patients that participate in the trials; ? the number of sites included in the trials; ? the countries in which the trials are conducted; ? the length of time required to enroll eligible patients; ? the number of doses that patients receive; ? the drop-out or discontinuation rates of patients;
? potential additional safety monitoring or other studies requested by
regulatory agencies; ? the impact of COVID-19 on the length of our trials; ? the duration of patient follow-up; and ? the efficacy and safety profile of the product candidates. 25 In addition, the probability of success for each product candidate will depend on numerous factors, including competition, manufacturing capability and commercial viability. We will determine which programs to pursue and fund in response to the scientific and clinical success of each product candidate, as well as an assessment of each product candidate's commercial potential. Because the product candidates are still in clinical and preclinical development and the outcome of these efforts is uncertain, we cannot estimate the actual amounts necessary to successfully complete the development and commercialization of product candidates or whether, or when, we may achieve profitability. Due to the early-stage nature of these programs, we do not track costs on a project-by-project basis. As these programs become more advanced, we intend to track the external and internal cost of each program. General and Administrative
General and administrative expenses consist primarily of salaries and other staff-related costs, including stock-based compensation for shares of common stock issued and options granted to founders, directors and personnel in executive, commercial, finance, accounting, legal, investor relations, facilities, business development and human resources functions and include vesting conditions.
Other significant general and administrative costs include costs relating to facilities and overhead costs, legal fees relating to corporate and patent matters, litigation,SEC filings, insurance, investor relations costs, fees for accounting and consulting services, and other general and administrative costs. General and administrative costs are expensed as incurred, and we accrue amounts for services provided by third parties related to the above expenses by monitoring the status of services provided and receiving estimates from our service providers and adjusting our accruals as actual costs become known. It is expected that the general and administrative expenses will increase over the next several years to support our continued research and development activities, manufacturing activities, potential commercialization of our product candidates and the increased costs of operating as a public company. These increases are anticipated to include increased costs related to the hiring of additional personnel, developing commercial infrastructure, fees to outside consultants, lawyers and accountants, and increased costs associated with being a public company, as well as expenses related to services associated with maintaining compliance with Nasdaq listing rules andSEC requirements, insurance and investor relations costs. Other Income
Other income primarily represents fees earned for research and development work performed for other companies, some of which are related parties.
Interest Expense
Interest expense consists primarily of interest expense related to debt instruments.
Gain (Loss) on Extinguishment of Convertible Notes
Gain (loss) on extinguishment of convertible notes represents the shortfall (excess) of the reacquisition cost of convertible notes as compared to their carrying value.
26
Change in Fair Value of Derivative Liabilities
Change in fair value of derivative liabilities represents the non-cash change in fair value of derivative liabilities during the reporting period. Gains resulting from change in fair value of derivative liabilities during the three months endedMarch 31, 2022 , were driven by decreases in stock price during the period, resulting in a lower fair value of the underlying liability.
Offering Costs Allocated to Warrant Liabilities
Change in offering costs allocated to warrant liabilities represents placement agent fees and offering expenses which were allocated to the PIPE Warrants and expensed immediately as they are liability classified.
Change in Fair Value of Accrued Issuable Equity
Change in fair value of accrued issuable equity represents the non-cash change in fair value of accrued equity prior to its formal issuance.
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