Clearmind Medicine Announces IRB Approval for FDA First-In-Human Clinical Trial of CMND-100 at Second Clinical Site
Clearmind Medicine Inc. (CMND)
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Company Research
Source: GlobeNewswire
FDA approval for the IND submission to conduct its trial already secured Vancouver, Canada, Oct. 10, 2024 (GLOBE NEWSWIRE) -- Clearmind Medicine Inc. (Nasdaq: CMND), (FSE: CWY0) (“Clearmind” or the "Company"), a clinical-stage biotech company focused on discovery and development of novel psychedelic-derived therapeutics to solve major under-treated health problems, today announced it has received Institutional Review Board (IRB) approval from one of its clinical sites in the U.S. for part A of its Phase I/IIa clinical trial in the United States for treating patients suffering from alcohol use disorder (AUD). The multinational, multi-center trial will assess the safety, tolerability, and pharmacokinetics of Clearmind’s innovative MEAI-based (5-methoxy-2-aminoindane) treatment, CMND-100. In addition to Johns Hopkins University, Maryland, USA, the trial will also take place at Yale School of Medicine, Connecticut, USA and IMCA Center in Ramat Gan, Israel. The Company has already
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News
- Clearmind Medicine Announces IRB Approval for FDA First-In-Human Clinical Trial of CMND-100 at Second Clinical Site [Yahoo! Finance]Yahoo! Finance
- Clearmind Medicine Announces the Notice of an International Patent Application for Pioneering Ibogaine Combination Therapy [Yahoo! Finance]Yahoo! Finance
- Clearmind Medicine Announces the Notice of an International Patent Application for Pioneering Ibogaine Combination TherapyGlobeNewswire
- Clearmind Medicine and Yissum File International Patent Application for Revolutionary Psychedelic Compounds for PTSD TreatmentGlobeNewswire
- Clearmind Medicine Announces Publication of International Patent Application for Innovative MDMA-Based Combination TreatmentGlobeNewswire
CMND
Sec Filings
- 11/20/24 - Form 6-K
- 11/14/24 - Form SC
- 10/10/24 - Form 6-K
- CMND's page on the SEC website