备受期待的美国食品和药物管理局(FDA)关于治疗创伤后应激障碍的迷幻剂的决定最终以拒绝而告终

Valerie A. Canady
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引用次数: 0

摘要

8月9日,美国食品和药物管理局(FDA)在一项备受关注的涉及使用迷幻疗法治疗创伤后应激障碍(PTSD)的决定中,拒绝批准使用亚甲二氧基甲基双氧安非他明(MDMA)辅助疗法治疗创伤后应激障碍。该联邦机构向MDMA辅助疗法的制药商Lykos Therapeutics公司签发了一份完整答复函(CRL)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Much anticipated FDA decision about psychedelics for PTSD ends with denial

In a closely watched decision involving the use of psychedelic treatment and therapy to treat post-traumatic stress disorder (PTSD), the U.S. Food and Drug Administration (FDA) on Aug. 9 declined to approve the use of midomafetamine (MDMA)-assisted therapy for the disorder. The federal agency issued a Complete Response Letter (CRL) for MDMA-assisted therapy to its drug maker, Lykos Therapeutics.

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