Clearmind Medicine Advances CMND-100 Clinical Trial After Positive Safety Review

Reuters11-24

<a href="https://laohu8.com/S/CMND">Clearmind Medicine</a> Advances CMND-100 Clinical Trial After Positive Safety Review

Clearmind Medicine Inc. has announced that its independent Data and Safety Monitoring Board (DSMB) has unanimously recommended the continuation of its ongoing FDA-approved Phase I/IIa clinical trial for CMND-100, a proprietary, non-hallucinogenic neuroplastogen, in the treatment of Alcohol Use Disorder (AUD). The recommendation follows a scheduled interim review based on encouraging top-line data from the first cohort, which demonstrated a favorable safety profile, with no serious adverse events reported and good tolerability among participants. The multinational, multi-center trial is evaluating the safety, tolerability, pharmacokinetics, and preliminary efficacy of CMND-100. The interim results have already been reviewed by the DSMB, supporting the continuation of the trial.

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: GNW9591193-en) on November 24, 2025, and is solely responsible for the information contained therein.

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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. <a href=\"https://laohu8.com/S/CMNDF\">Clearmind Medicine Inc.</a> published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW9591193-en) on November 24, 2025, and is solely responsible for the information contained therein.</span></em>\n</div></body></html>\n\n</article>\n</div>\n</body>\n</html>\n","isBrief":false,"type":0,"news_type":1,"symbol":"LU2210149790.SGD","symbol_name":"Natixis Thematics Subscription Economy R/A SGD-H","start_time":0,"source_url":"https://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20251124:nNDL8F88jL:1","article_id":"2585296467","we_media_id":"1032215980","thumbnails":[],"rights":null,"url":"https://stock-news.laohu8.com/highlight/detail?id=2585296467","pubTimestamp":1763992275,"columns":[],"sourceInfo":null,"weMediaInfo":{"media_name":"Reuters","introduction":"Reuters.com brings you the latest news from around the world, covering breaking news in markets, business, politics, entertainment and technology","home_visible":1,"id":"1032215980","head_image":"https://community-static.tradeup.com/news/4567337cbdf294b657b1fa87c5488b48"},"summary":"Clearmind Medicine Inc. has announced that its independent Data and Safety Monitoring Board  has unanimously recommended the continuation of its ongoing FDA-approved Phase I/IIa clinical trial for CMND-100, a proprietary, non-hallucinogenic neuroplastogen, in the treatment of Alcohol Use Disorder . 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The recommendation follows a scheduled interim review based on encouraging top-line data from the first cohort, which demonstrated a favorable safety profile, with no serious adverse events reported and good tolerability among participants. The multinational, multi-center trial is evaluating the safety, tolerability, pharmacokinetics, and preliminary efficacy of CMND-100. The interim results have already been reviewed by the DSMB, supporting the continuation of the trial.\n      \n\nDisclaimer: 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. 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