MDMA-Assisted Therapy for Post-Traumatic Stress Disorder: Regulatory Challenges and a Path Forward.

IF 7.4 2区 医学 Q1 CLINICAL NEUROLOGY
CNS drugs Pub Date : 2025-04-01 Epub Date: 2025-02-15 DOI:10.1007/s40263-025-01162-y
Balwinder Singh
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引用次数: 0

Abstract

Trauma is prevalent, with lifetime estimates of traumatic exposure ranging from 70% for a single event to 31% for multiple events. While many recover, a subset develop post-traumatic stress disorder (PTSD), a debilitating condition characterized by distressing memories, avoidance behaviors, hyperarousal, and mood disturbances. The National Comorbidity Survey reports a lifetime PTSD prevalence of 6.8%, with higher rates among women and veterans. PTSD is strongly associated with suicidality, depression, and substance use, and its chronic nature can cause significant functional impairment. Despite extensive research, only two US Food and Drug Administration (FDA)-approved medications, the selective serotonin reuptake inhibitors paroxetine and sertraline, are available for PTSD. Psychotherapy, including trauma-focused cognitive behavioral therapy, prolonged exposure therapy, and eye movement desensitization and reprocessing (EMDR), has shown efficacy. Recent interest has grown in using psychedelics and entactogens such as 3,4-methylenedioxymethamphetamine (MDMA) for PTSD. Early-phase clinical trials of MDMA-assisted therapy (MDMA-AT) showed promising results, leading the FDA to grant breakthrough therapy status to MDMA-AT in 2017. Phase 3 randomized controlled trials demonstrated significant reductions in PTSD symptoms, with nearly 70% of participants no longer meeting diagnostic criteria. However, in 2024, the FDA voted against MDMA approval, citing concerns about trial design (including blinding failure and lack of certain safety assessments including QT prolongation and abuse liability assessments), as well as concerns about allegations of potential misconduct. Ongoing research must address key challenges, including blinding, long-term safety, and variability in psychotherapy, to better understand the therapeutic potential of MDMA in PTSD treatment. The FDA's recent guidance on psychedelic trials provides a framework for future research. The objective of this article is to explore the potential of MDMA-AT in PTSD treatment, evaluate regulatory challenges following the FDA's recent decision, and highlight the need for ongoing research to address safety, efficacy, and therapeutic implementation.

mdma辅助治疗创伤后应激障碍:监管挑战和前进的道路。
创伤是普遍存在的,一生中创伤暴露的估计从单一事件的70%到多重事件的31%不等。虽然许多人康复了,但一小部分人患上了创伤后应激障碍(PTSD),这是一种以痛苦的记忆、逃避行为、过度觉醒和情绪障碍为特征的衰弱状态。美国国家共病调查报告称,PTSD终生患病率为6.8%,女性和退伍军人的患病率更高。创伤后应激障碍与自杀、抑郁和药物使用密切相关,其慢性性质可导致严重的功能损害。尽管进行了广泛的研究,但只有两种美国食品和药物管理局(FDA)批准的药物——选择性血清素再摄取抑制剂帕罗西汀和舍曲林——可用于治疗创伤后应激障碍。心理治疗,包括以创伤为中心的认知行为疗法、长时间暴露疗法和眼动脱敏和再加工(EMDR),已经显示出疗效。最近,人们对使用致幻剂和致幻剂如3,4-亚甲基二氧甲基苯丙胺(MDMA)治疗创伤后应激障碍的兴趣越来越大。mdma辅助治疗(MDMA-AT)的早期临床试验显示出令人鼓舞的结果,导致FDA在2017年授予MDMA-AT突破性治疗地位。3期随机对照试验显示创伤后应激障碍症状显著减轻,近70%的参与者不再符合诊断标准。然而,在2024年,FDA投票反对MDMA的批准,理由是对试验设计的担忧(包括盲法失败和缺乏某些安全性评估,包括QT延长和滥用责任评估),以及对潜在不当行为指控的担忧。正在进行的研究必须解决关键挑战,包括心理治疗的盲性、长期安全性和可变性,以更好地了解MDMA在PTSD治疗中的治疗潜力。FDA最近对迷幻药试验的指导为未来的研究提供了一个框架。本文的目的是探讨MDMA-AT在PTSD治疗中的潜力,评估FDA最近决定后的监管挑战,并强调需要进行持续研究以解决安全性、有效性和治疗实施问题。
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来源期刊
CNS drugs
CNS drugs 医学-精神病学
CiteScore
12.00
自引率
3.30%
发文量
82
审稿时长
6-12 weeks
期刊介绍: CNS Drugs promotes rational pharmacotherapy within the disciplines of clinical psychiatry and neurology. The Journal includes: - Overviews of contentious or emerging issues. - Comprehensive narrative reviews that provide an authoritative source of information on pharmacological approaches to managing neurological and psychiatric illnesses. - Systematic reviews that collate empirical evidence to answer a specific research question, using explicit, systematic methods as outlined by the PRISMA statement. - Adis Drug Reviews of the properties and place in therapy of both newer and established drugs in neurology and psychiatry. - Original research articles reporting the results of well-designed studies with a strong link to clinical practice, such as clinical pharmacodynamic and pharmacokinetic studies, clinical trials, meta-analyses, outcomes research, and pharmacoeconomic and pharmacoepidemiological studies. Additional digital features (including animated abstracts, video abstracts, slide decks, audio slides, instructional videos, infographics, podcasts and animations) can be published with articles; these are designed to increase the visibility, readership and educational value of the journal’s content. In addition, articles published in CNS Drugs may be accompanied by plain language summaries to assist readers who have some knowledge of, but not in-depth expertise in, the area to understand important medical advances.
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