GlobeNewsWire
13 Aug 2026, 11:36 UTC · 1h ago
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Clearmind Medicine's CMND-100 achieved its primary safety endpoint in Part A of its Phase I/II clinical trial, showing a favorable safety and tolerability profile. — Meeting primary safety endpoints is a critical de-risking event for clinical-stage biotech companies and is typically viewed as a prerequisite for any future valuation increase.
+0.60The Independent Data and Safety Monitoring Board (DSMB) has unanimously approved advancing the trial to Parts B and C, which include testing in patients with Alcohol Use Disorder (AUD). — Moving from healthy volunteers to the actual target patient population is a major clinical milestone that brings the company closer to demonstrating efficacy.
+0.40CMND-100 is designed as a non-hallucinogenic neuroplastogen, intending to avoid the perceptual effects and intensive clinical supervision required by classical psychedelics. — A non-hallucinogenic profile suggests a more scalable commercial model and lower regulatory hurdles compared to traditional psychedelic therapies.
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The company achieved its primary safety endpoint and received DSMB approval to advance its clinical trial of CMND-100 to patients with Alcohol Use Disorder.
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