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FDA Clears MindMed IND For MM-120 In Treatment Of Generalized Anxiety Disorder


Benzinga | Jan 25, 2022 07:33AM EST

FDA Clears MindMed IND For MM-120 In Treatment Of Generalized Anxiety Disorder

NEW YORK, Jan. 25, 2022 /PRNewswire/ -- Mind Medicine (MindMed) Inc. (NASDAQ:MNMD), (NEO: MMED), (DE: MMQ) (the "Company"), a clinical-stage biopharmaceutical company developing psychedelic-inspired therapies for the treatment of brain-based disorders, announced today that the U.S. Food and Drug Administration (FDA) has cleared MindMed's Investigational New Drug (IND) application, allowing the Company's Phase 2b dose-optimization trial of MM-120 for the treatment of generalized anxiety disorder (GAD) to proceed.






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