Clearmind Medicine Inc. reported that an independent Data and Safety Monitoring Board completed a second interim review of its ongoing FDA-approved Phase I/IIa clinical trial of CMND-100, a non-hallucinogenic neuroplastogen being studied for alcohol use disorder. The company said additional topline safety data from the second cohort of six participants showed no serious adverse events and supported continuation of the study, allowing progression to a third cohort with an 80 mg dose. The safety results have already been presented as topline findings, while further study results are expected in the future as the trial continues.
Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Clearmind Medicine Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: 202603040730PRIMZONEFULLFEED9665657) on March 04, 2026, and is solely responsible for the information contained therein.
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