Clearmind Medicine Inc. has announced the initiation of its FDA-approved Phase I/IIa clinical trial for CMND-100, a proprietary non-hallucinogenic MEAI-based oral drug candidate targeting Alcohol Use Disorder (AUD), at Hadassah Medical Center in Jerusalem, Israel. This addition brings the total number of global trial sites to five, including Yale, Johns Hopkins, Tel Aviv Sourasky, and IMCA. The multinational, multi-center study is designed to evaluate the safety, tolerability, pharmacokinetic profile, and preliminary efficacy of CMND-100 in reducing alcohol cravings and consumption among individuals with moderate to severe AUD. Top-line data from the first cohort have already been presented, demonstrating a favorable safety profile, strong treatment observance, and high adherence to the dosing regimen, with no serious adverse events reported. The study is ongoing.
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: GNW9579545-en) on November 20, 2025, and is solely responsible for the information contained therein.
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