Psychedelic drug MDMA faces FDA panel in bid to become first-of-a-kind PTSD medication

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Psychedelic drug MDMA faces FDA panel in bid to become first-of-a-kind PTSD medication
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Federal health advisers are weighing the first-of-a-kind approval of MDMA, the mind-altering club drug, as a treatment for PTSD

The Food and Drug Administration convened a panel of outside experts Tuesday to review the latest research on the drug, — part of a decadeslong effort by psychedelic advocates to win medical acceptance for the drug's purported benefits.convened a panel of outside experts Tuesday to review the latest research on the drug, which appears to show it can help relieve post-traumatic stress disorder when combined with talk therapy.

“This application is both consequential and complex,” FDA reviewer Dr. Tiffany R. Farchione said at the beginning of Tuesday's meeting. The FDA will ask its outside panel about that issue and several others, including uncertainty about how long the benefits of MDMA might last. About 25% of patients dropped out of a follow-up study designed to track long-term outcomes.

Representatives for drugmaker Lykos Therapeutics said Tuesday they agreed with such precautions and hoped that would hasten the drug's approval.

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