MIRA Pharmaceuticals (MIRA) risk factors, FY2025 10-K

MIRA Pharmaceuticals's FY2025 10-K, filed Mar 31, 2026, lists 65 risk factors in 7 groups. Against the prior year's 62: 9 new, 6 dropped, 9 substantially reworded.

Risk factors listed
657 groups
New this year
9vs 62 last year
Dropped
6since the prior 10-K
Substantially reworded
9of those kept
Section length
25k wordsItem 1A

What the changes say

  • MIRA expanded its risk factors around the SKNY acquisition and licensing of SKNY-1 from MIRALOGX.
  • Clinical trial risks now highlight the novel nature of synthetic cannabinoids and ketamine analogs.
  • Nasdaq listing compliance replaced general share dilution risks.

What changed since the prior 10-K

New

  • NewRisks Related to Our Operations and Financial Condition

    We are an early development-stage company with no revenues

    We are an early development-stage company with no revenues, a going concern explanatory paragraph, and significant liquidity needs.

  • NewRisks Related to Development and Regulatory Approval of Our Product Candidates

    Clinical trials for our product candidates are expensive, time-consuming, uncertain, and susceptible to change, delay or termination. The results of clinical trials are open to differing interpretations

    Our clinical trials are subject to expensive, time-consuming delays and suspensions by the FDA, IRBs, or DEA quota restrictions.

  • NewRisks Related to SKNY and SKNY-1

    SKNY has yet to generate revenues or achieve a profit and may not generate revenue or achieve a profit for many years, if at all

    SKNY has no revenues or profit and depends entirely on future regulatory approvals to commercialize its product candidates.

  • NewRisks Related to SKNY and SKNY-1

    SKNY does not own rights to SKNY-1

    SKNY does not own SKNY-1 and holds only a limited license in the US, Canada, and Mexico from MIRALOGX.

  • NewRisks Related to SKNY and SKNY-1

    SKNY’s rights to SKNY-1 are subject to royalties

    SKNY owes MIRALOGX an 8% royalty with a minimum annual payment of $250,000 starting in the first revenue year.

  • NewRisks Related to SKNY and SKNY-1

    Conflicts of interest may arise between SKNY and MIRALOGX

    Conflicts of interest may arise between SKNY and its licensor MIRALOGX, which is owned by our largest stockholder, the Bay Shore Trust.

  • NewRisks Related to SKNY and SKNY-1

    SKNY’s product candidates, if approved, may not achieve the expected market acceptance and, consequently, limit SKNY’s ability to generate revenue

    SKNY's product candidates may fail to achieve market acceptance by physicians and patients even if regulatory approval is obtained.

  • NewRisks Related to SKNY and SKNY-1

    SKNY expects to face intense competition, often from companies with greater resources and experience than it has

    SKNY expects intense competition from multinational pharmaceutical companies, specialized biotechnology firms, and research institutions.

  • NewRisks Related to SKNY and SKNY-1

    We are dependent on SKNY’s current and future product candidates, some of which may not receive regulatory approval or be successfully commercialized

    Our growth depends entirely on SKNY's ability to successfully develop, manufacture, and commercialize SKNY product candidates.

Dropped

  • DroppedRisks Related to Our Reliance Upon Third Parties

    We rely on, and expect to continue to rely on, third parties to conduct clinical trials for our product candidates

  • DroppedRisks Related to Our Operations and Financial Condition

    We may not be successful in the integration of our potential acquisition of SKNY

  • DroppedRisks Relating to Our Business and Our Industry

    Should we later determine if it is in our best interest to develop a sales force, we may be unable to effectively train and equip our sales force, therefore our ability to successfully commercialize our products may be harmed

    We rely on third parties to conduct clinical trials.

  • DroppedRisks Relating to Our Business and Our Industry

    Our management and personnel, systems, and facilities currently in place may not be adequate to support our business plan and future growth. As a result, we may need to further expand certain areas of our organization

  • DroppedRisks Related to Development and Regulatory Approval of Our Product Candidates

    We are subject to extensive regulation by U.S. federal and state governments in each of the markets where we have product candidates progressing through the approval process

  • DroppedRisks Related to Our Reliance Upon Third Parties

    We maintain our cash at financial institutions, at times in balances that exceed federally insured limits. The failure of financial institutions could adversely affect our ability to pay operational expenses or make other payments

    Risks related to the potential acquisition of SKNY.

Reworded

  • 100% rewrittenRisks Related to Development and Regulatory Approval of Our Product Candidates

    Clinical trials for our product candidates are expensive, time-consuming, uncertain, and susceptible to change, delay or termination. The results of clinical trials are open to differing interpretations

    Updated to focus specifically on the novel and unpredictable trial risks of synthetic cannabinoid drug candidates and ketamine analogs.

  • 100% rewrittenRisks Relating to the Ownership of our Common Stock

    Sales of a significant number of shares of our common stock in the public markets, or the perception that such sales could occur, could depress the market price of our common stock

    Replaced share dilution and shelf registration risks with the risk of being delisted from Nasdaq for non-compliance.

  • 100% rewrittenRisks Relating to Our Business and Our Industry

    Results of pre-clinical studies and earlier clinical trials are not necessarily predictive indicators of future results

    Expanded to specify that pre-clinical success does not predict Phase I, II, or III trial outcomes due to varying data interpretations.

  • 100% rewrittenRisks Related to Our Intellectual Property

    If third parties claim that our intellectual property, products, processes, or anything else used by us infringes upon their intellectual property, our operating profits could be adversely affected

    Added the threat of broader patent litigation in the pharmaceutical industry regarding intellectual property infringement claims.

  • 92% rewrittenRisks Related to Our Reliance Upon Third Parties

    We depend on a limited number of suppliers for materials and components required to manufacture our product candidates. The loss of these suppliers, or their failure to supply us on a timely basis, could cause delays in our current and future capacity and adversely affect our business

    Retained supplier concentration risks without substantive textual changes.

  • 71% rewrittenRisks Related to Our Intellectual Property

    We may not be able to adequately protect our product candidates or our proprietary technology in the marketplace

    Retained intellectual property protection and natural compound patent difficulties without substantive textual changes.

  • 69% rewrittenRisks Relating to the Ownership of our Common Stock

    Certain of our founding stockholders, plus our existing officers and directors, control a substantial interest in us and thus may influence certain actions requiring stockholder vote

    Added a reference regarding public market sales of common stock by controlling stockholders Bay Shore Trust and MIRALOGX.

  • 57% rewrittenRisks Relating to Our Business and Our Industry

    Impact of global tensions may increase uncertainty of our future operations

    Retained macroeconomic uncertainties and clinical trial disruptions from the Palestine-Israel and Ukraine wars without changes.

  • 27% rewrittenRisks Related to Our Operations and Financial Condition

    Certain of our executive officers will not be employed by us on a full-time basis

All 65 risk factors

Headings as the filing states them, in filing order.

Risks Related to Our Operations and Financial Condition

  1. 01We are an early development-stage company with no revenuesNew
  2. 04We are an early development-stage company with no revenues. As such, our losses from operations and negative cash flows as of December 31, 2025 raise substantial doubt about our ability to continue as a going concern absent obtaining adequate new debt or equity financings
  3. 05The report of our independent registered accounting firm on our audited financial statements for the fiscal year ended December 31, 2025 contains an explanatory paragraph relating to our ability to continue as a going concern
  4. 06Because we have a limited operating history, you may not be able to accurately evaluate our operations
  5. 07We have significant and increasing liquidity needs and will require additional funding
  6. 08Operating results may vary significantly in future periods
  7. 09We have yet to generate revenues or achieve a profit and may not generate revenue or achieve a profit for many years, if at all
  8. 10Conflicts of interest may arise between us and MIRALOGX
  9. 11Certain of our executive officers will not be employed by us on a full-time basis27% rewritten

Risks Related to Development and Regulatory Approval of Our Product Candidates

  1. 02Clinical trials for our product candidates are expensive, time-consuming, uncertain, and susceptible to change, delay or termination. The results of clinical trials are open to differing interpretations100% rewritten
  2. 33Clinical trials for our product candidates are expensive, time-consuming, uncertain, and susceptible to change, delay or termination. The results of clinical trials are open to differing interpretationsNew
  3. 34Clinical trials of synthetic cannabinoid drug candidates and ketamine analogs are novel with very limited or non-existing history; we face a significant risk that the trials will not result in commercially viable drugs and treatments
  4. 35We are subject to federal and state healthcare laws and regulations and implementation of or changes to such healthcare laws and regulations could adversely affect our business and results of operations
  5. 36We plan to conduct clinical trials at sites outside the United States. The FDA may not accept data from trials conducted in such locations, and the conduct of trials outside the United States could subject us to additional delays and expense
  6. 37The regulatory approval processes with the FDA are lengthy and inherently unpredictable
  7. 38There is a high rate of failure for drug candidates proceeding through clinical trials
  8. 39If we are found in violation of federal or state “fraud and abuse” laws, we may be required to pay a penalty and/or be suspended from participation in federal or state health care programs, which may adversely affect our business, financial condition, and results of operations
  9. 40Serious adverse events or other safety risks could require us to abandon development and preclude, delay or limit approval of our product candidates, limit the scope of any approved label or market acceptance, or cause the recall or loss of marketing approval of products that are already marketed

Risks Relating to the Ownership of our Common Stock

  1. 03Sales of a significant number of shares of our common stock in the public markets, or the perception that such sales could occur, could depress the market price of our common stock100% rewritten
  2. 53Because of the speculative nature of investment risk, you may lose your entire investment
  3. 54Certain of our founding stockholders, plus our existing officers and directors, control a substantial interest in us and thus may influence certain actions requiring stockholder vote69% rewritten
  4. 55The requirements of being a public company may strain our resources, divert management’s attention and affect our ability to attract and retain executive management and qualified board members
  5. 56We are an “emerging growth company,” and any decision on our part to comply only with certain reduced reporting and disclosure requirements applicable to emerging growth companies could make shares of our common stock less attractive to investors
  6. 57Investors could find our shares less attractive if we choose to rely on these exemptions. If some investors find shares less attractive as a result of any choice to reduce future disclosure, there may be a less active trading market for our shares and our share price may be more volatile
  7. 58If we fail to maintain compliance with Nasdaq Listing Rules, our shares may be delisted from Nasdaq, which would result in a limited trading market for our shares and make obtaining future debt or equity financing more difficult for the us
  8. 59If our shares were to be delisted from Nasdaq, they may become subject to the SEC’s “penny stock” rules
  9. 60Our status as a Florida corporation and the anti-takeover provisions of the Florida Business Corporation Act, which we sometimes refer to as the FBCA, may discourage, delay or prevent a change in control even if a change in control would be beneficial to our shareholders
  10. 61Both the control share acquisition statute and the affiliated transactions statute may have the effect of discouraging or preventing certain change of control or takeover transactions involving us
  11. 62Securities or industry analysts may not regularly publish reports on us, which could cause the price of our securities or trading volumes to decline
  12. 63We will likely conduct further offerings of our equity securities in the future, in which case your proportionate interest may become diluted
  13. 64We may issue shares of preferred stock in the future, which could make it difficult for another company to acquire us or could otherwise adversely affect holders of our common stock, which could depress the price of our common stock
  14. 65We have never declared or paid any cash dividends or distributions on our capital stock. We currently intend to retain our future earnings, if any, to support operations and to finance expansion and therefore we do not anticipate paying any cash dividends on our common stock in the foreseeable future

Risks Relating to Our Business and Our Industry

  1. 12Our future viability will largely depend on the positive development of Ketamir-2 and MIRA-55, and any future product candidates, which development will require significant capital resources and years of clinical development effort
  2. 13We are dependent on our current and future product candidates, some of which may not receive regulatory approval or be successfully commercialized
  3. 14Impact of global tensions may increase uncertainty of our future operations57% rewritten
  4. 15Results of pre-clinical studies and earlier clinical trials are not necessarily predictive indicators of future results100% rewritten
  5. 16We have limited marketing experience, and we do not anticipate at this time establishing a sales force or distribution and reimbursement capabilities, and we may not be able to successfully commercialize any of our product candidates if they are approved in the future
  6. 17Our product candidates, if approved, may be unable to achieve the expected market acceptance and, consequently, limit our ability to generate revenue from new products
  7. 18If the price for any future approved products decreases or if government and other third-party payers do not provide coverage and adequate reimbursement levels, our revenue and prospects for profitability will suffer
  8. 19We expect to face intense competition, often from companies with greater resources and experience than we have
  9. 20Product shipment delays could have a material adverse effect on our business, results of operations and financial condition
  10. 21Business interruptions could delay us in the process of developing our product candidates and could disrupt our product sales
  11. 22If product liability lawsuits are successfully brought against us, we will incur substantial liabilities and may be required to limit the commercialization of Ketamir-2 and MIRA-55 and our product candidates
  12. 23Counterfeit versions of our products could harm our business
  13. 24We depend upon our key personnel and our ability to attract and retain employees
  14. 25Our employees may engage in misconduct or other improper activities, including noncompliance with regulatory standards and requirements
  15. 26Our proprietary information, or that of our suppliers and business partners, may be lost or we may suffer security breaches
  16. 27Failure of our information technology systems, including cybersecurity attacks or other data security incidents, could significantly disrupt the operation of our business
  17. 28Security breaches, loss of data and other disruptions could compromise sensitive information related to our business, prevent us from accessing critical information or expose us to liability, which could adversely affect our business and our reputation
  18. 29Legislative or regulatory reform of the health care system in the U.S. may affect our ability to profitably sell our products, if approved
  19. 30We expect additional federal and state legislative proposals for health care reform, which could limit the prices that can be charged for the products we develop and may limit our commercial opportunity
  20. 31Unfavorable global economic and geopolitical conditions could adversely affect our business, financial condition, stock price, and results of operations
  21. 32We may acquire other companies which could divert our management’s attention, result in additional dilution to our shareholders and otherwise disrupt our operations and harm our operating results

Risks Related to Our Reliance Upon Third Parties

  1. 41Our existing collaboration arrangements and any that we may enter into in the future may not be successful, which could adversely affect our ability to develop and commercialize our product candidates
  2. 42We depend on a limited number of suppliers for materials and components required to manufacture our product candidates. The loss of these suppliers, or their failure to supply us on a timely basis, could cause delays in our current and future capacity and adversely affect our business92% rewritten

Risks Related to Our Intellectual Property

  1. 43We may not be able to adequately protect our product candidates or our proprietary technology in the marketplace71% rewritten
  2. 44If third parties claim that our intellectual property, products, processes, or anything else used by us infringes upon their intellectual property, our operating profits could be adversely affected100% rewritten
  3. 45We have no patent protection for MIRA-55, which could adversely impact MIRA-55’s potential competitive position

Risks Related to SKNY and SKNY-1

  1. 46SKNY has yet to generate revenues or achieve a profit and may not generate revenue or achieve a profit for many years, if at allNew
  2. 47SKNY does not own rights to SKNY-1New
  3. 48SKNY’s rights to SKNY-1 are subject to royaltiesNew
  4. 49Conflicts of interest may arise between SKNY and MIRALOGXNew
  5. 50SKNY’s product candidates, if approved, may not achieve the expected market acceptance and, consequently, limit SKNY’s ability to generate revenueNew
  6. 51SKNY expects to face intense competition, often from companies with greater resources and experience than it hasNew
  7. 52We are dependent on SKNY’s current and future product candidates, some of which may not receive regulatory approval or be successfully commercializedNew

Other MIRA Pharmaceuticals 10-Ks

  • FY2024 10-K risk factors
    62 risks

    MIRA Pharmaceuticals faces substantial going concern doubt with an accumulated deficit of $29.1 million as of December 31, 2024. The company depends entirely on the success of pre-clinical candidates Ketamir-2 and MIRA-55. Operations rely heavily on third-party contractors for manufacturing and clinical trials.

    Filed Mar 28, 2025

About this page

The headings are the filing's own. The one-line readings and the overview are automated and can be wrong: read Item 1A of the 10-K for the exact wording.