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Research LSD FDA-Approved Clinical Trials for Anxiety

Electrum1

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Nov 22, 2021
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MindMed got FDA breakthrough designation for their LSD trial last month

Food and Drug Administration has granted breakthrough designation for its MM120 LSD-based treatment for generalized anxiety disorder
“That MM120 exhibited rapid and robust efficacy, solidly sustained for 12 weeks after a single dose, is truly remarkable,” said David Feifel, professor emeritus of psychiatry at the University of California, San Diego, and director of the Kadima Neuropsychiatry Institute in La Jolla, Calif. Feifel was an investigator on the MM120 study.

MindMed is now planning to hold end-of-Phase 2 meetings with the FDA in the first half of the year and aims to initiate a Phase 3 trial in the second half of 2024.


Positive phase 2 results press release:
 
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