Press Releases June 16, 2026 07:32 AM

Clearmind Medicine Completes Dosing for Part A of its of FDA-Regulated Phase I/II Clinical Trial

Clearmind Medicine successfully completes dosing for Part A of Phase I/II FDA-regulated clinical trial targeting Alcohol Use Disorder.

By Jordan Park
Share
Twitter Reddit Facebook LinkedIn
CMND

Clearmind Medicine Inc. announced the successful completion of dosing for all 24 participants in Part A of its Phase I/II clinical trial evaluating CMND-100 for Alcohol Use Disorder treatment. The study is conducted under FDA oversight across multiple leading clinical sites, showing a strong safety profile with promising interim results, reflecting progress in developing non-hallucinogenic neuroplastogen-derived therapeutics.

Clearmind Medicine Completes Dosing for Part A of its of FDA-Regulated Phase I/II Clinical Trial
CMND
Summarize with
ChatGPT Perplexity Claude Grok Gemini

Key Points

  • Completion of dosing for all 24 participants in Part A of the Phase I/II clinical trial.
  • Trial conducted under FDA oversight across prestigious institutions in the US and Israel, emphasizing regulatory compliance.
  • Interim results indicate a strong safety profile for CMND-100, supporting further clinical development.

Vancouver, Canada, June 16, 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, neuroplastogen-derived therapeutics to solve major under-treated health problems, today announced the successful completion of dosing for all 24 participants in Cohorts 1 through 4 of Part A of its ongoing Phase I/II clinical trial evaluating CMND-100 for the treatment of Alcohol Use Disorder (AUD).

All healthy participants in the first stage of the trial have been treated with escalating  dose levels of the Company’s proprietary drug candidate, CMND-100. All trial sites, including Yale School of Medicine, Johns Hopkins University School of Medicine, Tel Aviv Sourasky Medical Center, and Hadassah Medical Center, demonstrated rapid patient recruitment and efficient treatment timelines.

“We are very pleased to have completed dosing of all 24 participants in the first four cohorts marking the completion of Part A of the clinical trial, supported by the rapid enrollment and excellent execution across our leading clinical sites in Israel and the United States,” said Adi Zuloff-Shani, PhD, CEO of Clearmind Medicine. “The interim results from the first three cohorts continue to show a strong safety profile, which is encouraging as we advance this important program under FDA oversight.”

The ongoing Phase I/II trial is being conducted under FDA oversight (IND) as a multicenter, randomized, double-blind, placebo-controlled study

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 trial and how interim results from the first three cohorts continue to show a strong safety profile, which is encouraging as it advances its clinical study under FDA oversight. 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.


Risks

  • Clinical trial outcomes remain uncertain and may not demonstrate efficacy or safety in later phases, impacting regulatory approval.
  • Dependence on FDA regulatory processes which may delay or complicate drug approval and commercialization timelines.
  • Potential market competition from other treatments for Alcohol Use Disorder could affect commercial success.

More from Press Releases

Virtuix Expands Defense Presence at TSIS 2026 Following U.S. Air Force Award and Marine Corps Collaboration Jun 16, 2026 Nexalin Technology Announces Two Clinical Abstracts Accepted for Presentation at the 2026 NYC Neuromodulation Conference Highlighting Preliminary Clinical Results Across Anxiety, Depression, Insomnia and Quality of Life Jun 16, 2026 Trinity Biotech Awarded Significant Orders for Over 2 Million TrinScreen HIV Tests And Reports Q1 2026 Financial Results Jun 16, 2026 SEALSQ Secures Patent for Breakthrough “Back-to-Physical” NFT Technology Jun 16, 2026 For Kyivstar Customers in Ukraine, Out of Coverage No Longer Means Out of Touch Jun 16, 2026