Neuroscape, Department of Neurology, University of California, San Francisco, San Francisco, CA, USA.
Department of Psychiatry and Behavioral Sciences, University of California, San Francisco, San Francisco, CA, USA.
Nat Med. 2023 Oct;29(10):2473-2480. doi: 10.1038/s41591-023-02565-4. Epub 2023 Sep 14.
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 .
这项多中心、随机、双盲、确证性 3 期研究评估了 3,4-亚甲二氧基甲基苯丙胺辅助治疗(MDMA-AT)与安慰剂加相同治疗在中重度创伤后应激障碍(PTSD)患者中的疗效和安全性。使用盲法独立评估员评估了临床医生管理的 PTSD 量表 5 版(CAPS-5)总严重程度评分(主要终点)和 Sheehan 残疾量表(SDS)功能损伤评分(关键次要终点)的变化。参与者被随机分配到 MDMA-AT(n=53)或安慰剂加治疗(n=51)。总体而言,26.9%(28/104)的参与者有中度 PTSD,73.1%(76/104)的参与者有重度 PTSD。参与者在种族上多种多样:104 名参与者中有 28 名(26.9%)是西班牙裔/拉丁裔,104 名参与者中有 35 名(33.7%)是非白种人。最小二乘(LS)平均 CAPS-5 评分变化(95%置信区间(CI))为 MDMA-AT 组为-23.7(-26.94,-20.44),安慰剂加治疗组为-14.8(-18.28,-11.28)(P<0.001,d=0.7)。LS 平均 SDS 评分变化(95%CI)为 MDMA-AT 组为-3.3(-4.03,-2.60),安慰剂加治疗组为-2.1(-2.89,-1.33)(P=0.03,d=0.4)。7 名参与者出现严重治疗出现的不良事件(TEAE)(MDMA-AT 组,n=5(9.4%);安慰剂加治疗组,n=2(3.9%))。无死亡或严重 TEAE。这些数据表明,MDMA-AT 降低了中重度 PTSD 患者的 PTSD 症状和功能障碍,且总体耐受性良好。临床试验.gov 标识符:NCT04077437。