Back to the drawing board for Lykos' MDMA therapy

Alison Knopf
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Abstract

The Food and Drug Administration (FDA) did not accept the application of Lykos Therapeutics for MDMA as a treatment for post-traumatic stress disorder (PTSD). In a letter dated Aug. 9 and released by Lykos Therapeutics, the for-profit arm of the Multidisciplinary Association for Psychedelic Studies (MAPS), the company stated that it is disappointed in the FDA response, but that it intends to pursue the goal of approval. This announcement was followed by the retraction of three peer-reviewed studies on Aug. 9 as well. The FDA did not completely reject the idea of ever approving MDMA, but asked Lykos for more information.

莱科斯的摇头丸疗法又回到了起点
美国食品和药物管理局(FDA)没有接受Lykos Therapeutics公司将摇头丸作为创伤后应激障碍(PTSD)治疗药物的申请。Lykos Therapeutics公司是多学科迷幻剂研究协会(MAPS)的营利机构,该公司在8月9日发布的一封信中表示,它对FDA的答复感到失望,但它打算继续追求获得批准的目标。在这一声明发布后,8 月 9 日又撤回了三项经同行评审的研究。FDA 并未完全拒绝批准摇头丸的想法,但要求 Lykos 提供更多信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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