Clearmind Medicine's CMND-100 successfully met safety endpoints in a Phase I/IIa trial for Alcohol Use Disorder.
Quiver AI Summary
Clearmind Medicine Inc. has announced positive results from its Phase I/IIa clinical trial of CMND-100, a non-hallucinogenic oral drug candidate for treating Alcohol Use Disorder (AUD). The trial met its primary endpoint, demonstrating a high safety profile for CMND-100, particularly in the third cohort where no serious adverse events were reported. The multinational study evaluated the drug's safety, tolerability, pharmacokinetics, and preliminary efficacy in patients with moderate to severe AUD. The favorable outcomes support the further development of CMND-100 as a potential innovative treatment for AUD. Clearmind, a biotech focused on non-hallucinogenic psychedelic therapies, holds 31 granted patents in its intellectual portfolio and is listed on Nasdaq under the symbol "CMND."
Potential Positives
- Clearmind Medicine has successfully met the primary endpoint in its FDA-approved Phase I/IIa clinical trial for its non-hallucinogenic drug candidate CMND-100, indicating progress in its development.
- The clinical trial results show a high safety profile for CMND-100, with no serious adverse events reported in the third cohort, supporting the drug's potential as a treatment for Alcohol Use Disorder.
- The multinational and multicenter design of the trial demonstrates Clearmind's commitment to thorough evaluation, which may enhance its credibility and attractiveness to investors and partners.
- Clearmind holds a robust intellectual property portfolio with 31 granted patents, positioning the company well for future innovations and commercialization opportunities.
Potential Negatives
- The press release emphasizes the use of forward-looking statements, indicating inherent uncertainties and risks associated with the company's clinical trials and projections, which may lead to less investor confidence.
- Despite the reporting of safety and tolerability, the clinical trial is still in the early phase, and the overall efficacy of CMND-100 for treating Alcohol Use Disorder remains unproven, which could affect future investment and development plans.
- There is a lack of detailed information regarding competitive landscape and the potential market challenges for CMND-100, which may raise concerns among stakeholders about the drug's commercial viability.
FAQ
What is Clearmind Medicine focused on?
Clearmind Medicine focuses on developing non-hallucinogenic psychedelics and neuroplastogen-derived therapeutics for under-treated health problems.
What is CMND-100?
CMND-100 is Clearmind's proprietary oral drug candidate designed to treat Alcohol Use Disorder (AUD) with a non-hallucinogenic approach.
What were the results of the Phase I/IIa trial for CMND-100?
The Phase I/IIa trial showed CMND-100 met its primary endpoint with a high safety profile and good tolerability.
How many patent families does Clearmind have?
Clearmind has a portfolio consisting of nineteen patent families, with a total of 31 granted patents.
Where can I find more information about Clearmind Medicine?
More information about Clearmind Medicine can be found on their official website at www.clearmindmedicine.com.
Disclaimer: This is an AI-generated summary of a press release distributed by GlobeNewswire. The model used to summarize this release may make mistakes. See the full release here.
$CMND Hedge Fund Activity
We have seen 1 institutional investors add shares of $CMND stock to their portfolio, and 6 decrease their positions in their most recent quarter.
Here are some of the largest recent moves:
- ADVISORSHARES INVESTMENTS LLC removed 217,746 shares (-97.0%) from their portfolio in Q4 2025, for an estimated $394,120
- VIRTU FINANCIAL LLC removed 28,554 shares (-100.0%) from their portfolio in Q4 2025, for an estimated $51,682
- SUSQUEHANNA INTERNATIONAL GROUP, LLP removed 24,292 shares (-100.0%) from their portfolio in Q4 2025, for an estimated $43,968
- MORGAN STANLEY removed 2,564 shares (-100.0%) from their portfolio in Q4 2025, for an estimated $4,640
- NATIONAL BANK OF CANADA /FI/ removed 379 shares (-100.0%) from their portfolio in Q4 2025, for an estimated $685
- OSAIC HOLDINGS, INC. removed 10 shares (-100.0%) from their portfolio in Q4 2025, for an estimated $18
- JPMORGAN CHASE & CO added 5 shares (+inf%) to their portfolio in Q4 2025, for an estimated $9
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Full Release
Vancouver, Canada, April 20, 2026 (GLOBE NEWSWIRE) -- Clearmind Medicine Inc. (Nasdaq: CMND) (“Clearmind” or the "Company"), a clinical-stage biotech company focused on the discovery and development of novel, non-hallucinogenic, second generation psychedelic, neuroplastogen-derived therapeutics to solve major under-treated health problems, recently announced that CMND-100, the Company’s proprietary non-hallucinogenic MEAI-based oral drug candidate, for the treatment of Alcohol Use Disorder (AUD) has met the primary endpoint in its FDA-approved Phase I/IIa clinical trial.
Results from the third cohort of the trial indicated a high safety profile for CMND-100, even at the higher dosage administered to date. The data demonstrated that the drug candidate was well tolerated, with no serious adverse events reported in the third cohort and continued favorable overall tolerability, consistent with the safety outcomes observed in prior cohorts.
The Phase I/IIa clinical trial is a multinational, multicenter study designed to evaluate the safety, tolerability, pharmacokinetics, and preliminary efficacy of CMND-100 in patients with moderate to severe AUD. Meeting the primary safety and tolerability endpoint in this dose-escalation stage, including at the higher dosage in the third cohort, supports continued advancement of CMND-100 as a potential novel, non-hallucinogenic treatment option for AUD.
About Clearmind Medicine Inc.
Clearmind is a clinical-stage neuroplastogens pharmaceutical biotech company focused on the discovery and development of non-hallucinogenic, second generation, neuroplastogen-derived therapeutics to solve widespread and underserved health problems, including alcohol use disorder. Its primary objective is to research and develop psychedelic-based compounds and attempt to commercialize them as regulated medicines, foods, or supplements.
The Company’s intellectual portfolio currently consists of nineteen patent families, including 31 granted patents. The Company intends to seek additional patents for its compounds whenever warranted and will remain opportunistic regarding the acquisition of additional intellectual property to build its portfolio.
Shares of Clearmind are listed for trading on Nasdaq under the symbol "CMND."
For further information, visit: https://www.clearmindmedicine.com or contact:
Investor Relations
[email protected]
www.Clearmindmedicine.com
Forward-Looking Statements:
This press release contains “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act and other securities laws. Words such as “expects,” “anticipates,” “intends,” “plans,” “believes,” “seeks,” “estimates” and similar expressions or variations of such words are intended to identify forward-looking statements. For example, the Company is using forward-looking statements when it discusses the timing and progress of its clinical trials. Forward-looking statements are not historical facts, and are based upon management’s current expectations, beliefs and projections, many of which, by their nature, are inherently uncertain. Such expectations, beliefs and projections are expressed in good faith. However, there can be no assurance that management’s expectations, beliefs and projections will be achieved, and actual results may differ materially from what is expressed in or indicated by the forward-looking statements. Forward-looking statements are subject to risks and uncertainties that could cause actual performance or results to differ materially from those expressed in the forward-looking statements. For a more detailed description of the risks and uncertainties affecting the Company, reference is made to the Company’s reports filed from time to time with the Securities and Exchange Commission (“SEC”), including, but not limited to, the risks detailed in the Company’s annual report on Form 20-F for the fiscal year ended October 31, 2025 and subsequent filings with the SEC. Forward-looking statements speak only as of the date the statements are made. The Company assumes no obligation to update forward-looking statements to reflect actual results, subsequent events or circumstances, changes in assumptions or changes in other factors affecting forward-looking information except to the extent required by applicable securities laws. If the Company does update one or more forward-looking statements, no inference should be drawn that the Company will make additional updates with respect thereto or with respect to other forward-looking statements. References and links to websites have been provided as a convenience, and the information contained on such websites is not incorporated by reference into this press release. Clearmind is not responsible for the contents of third-party websites.