MDMA-assisted therapy for moderate to severe PTSD: a randomized, placebo-controlled phase 3 trial

MDMA公司 安慰剂 随机对照试验 医学 精神科 内科学 替代医学 病理
作者
Jennifer Mitchell,Marcela Ot’alora G.,Bessel van der Kolk,Scott Shannon,Michael P. Bogenschutz,Yevgeniy Gelfand,Casey Paleos,Christopher R. Nicholas,Sylvestre Quevedo,Brooke Balliett,Scott Hamilton,Michael C. Mithoefer,Sarah E. Kleiman,Kelly Parker-Guilbert,Keren Tzarfaty,Charlotte Harrison,Alberdina de Boer,Rick Doblin,Berra Yazar‐Klosinski,Charlotte Harrison
出处
期刊:Nature Medicine [Nature Portfolio]
卷期号:29 (10): 2473-2480 被引量:240
标识
DOI:10.1038/s41591-023-02565-4
摘要

This multi-site, randomized, double-blind, confirmatory phase 3 study evaluated the efficacy and safety of 3,4-methylenedioxymethamphetamine-assisted therapy (MDMA-AT) versus placebo with identical therapy in participants with moderate to severe post-traumatic stress disorder (PTSD). Changes in Clinician-Administered PTSD Scale for DSM-5 (CAPS-5) total severity score (primary endpoint) and Sheehan Disability Scale (SDS) functional impairment score (key secondary endpoint) were assessed by blinded independent assessors. Participants were randomized to MDMA-AT (n = 53) or placebo with therapy (n = 51). Overall, 26.9% (28/104) of participants had moderate PTSD, and 73.1% (76/104) of participants had severe PTSD. Participants were ethnoracially diverse: 28 of 104 (26.9%) identified as Hispanic/Latino, and 35 of 104 (33.7%) identified as other than White. Least squares (LS) mean change in CAPS-5 score (95% confidence interval (CI)) was -23.7 (-26.94, -20.44) for MDMA-AT versus -14.8 (-18.28, -11.28) for placebo with therapy (P < 0.001, d = 0.7). LS mean change in SDS score (95% CI) was -3.3 (-4.03, -2.60) for MDMA-AT versus -2.1 (-2.89, -1.33) for placebo with therapy (P = 0.03, d = 0.4). Seven participants had a severe treatment emergent adverse event (TEAE) (MDMA-AT, n = 5 (9.4%); placebo with therapy, n = 2 (3.9%)). There were no deaths or serious TEAEs. These data suggest that MDMA-AT reduced PTSD symptoms and functional impairment in a diverse population with moderate to severe PTSD and was generally well tolerated. ClinicalTrials.gov identifier: NCT04077437 .
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