迷幻药医疗化的知识差距:临床研究和监管问题

Drummond E-Wen McCulloch , Matthias E. Liechti , Kim PC. Kuypers , David Nutt , Johan Lundberg , Dea Siggaard Stenbæk , Guy M. Goodwin , Gerhard Gründer , Florence Butlen-Ducuing , Marion Haberkamp , Steffen Thirstrup , Gitte M. Knudsen
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引用次数: 0

摘要

包括迷幻药和迷幻剂在内的迷幻药物正在针对一系列精神和神经疾病进行临床试验,尤其是在抑郁症的第二阶段研究中显示出了巨大的前景。在这篇文章中,我们概述了欧洲神经精神药理学学院成员在尼斯新前沿会议(2023 年)上指出的迷幻药作为药物成功实施可能必须弥补的关键知识差距。关键主题包括药代动力学和药效学特征、迷幻药之间的比较、主观效应持续时间与治疗效果之间的关系、多药理学以及心理支持的影响。最后,我们将从欧洲药品管理局和健康技术评估师的角度来探讨欧洲医疗实施的最迫切要求。
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Knowledge gaps in psychedelic medicalisation: Clinical studies and regulatory aspects

Psychedelic drugs including psilocybin and LSD are undergoing clinical trials for a range of psychiatric and neurological conditions, and have particularly shown substantial promise in phase 2 studies of depression. In this article we outline key knowledge gaps that may be imperative for a successful implementation of psychedelic drugs as medicines as identified by members of the European College of Neuropsychopharmacology at the New Frontiers Meeting in Nice (2023). Key themes include pharmacokinetic and pharmacodynamic characterisation, comparisons between psychedelics, the relation between the duration of subjective effects and therapeutic outcomes, polypharmacology, and the impact of psychological support. We conclude with a perspective from the European Medicines Agency and Heath Technology Assessors on the most pressing requirements for medical implementation in Europe.

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