PinneyAssociates, Inc, 4800 Montgomery Lane, Suite 400, Bethesda, MD, USA; Department of Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
PinneyAssociates, Inc, 4800 Montgomery Lane, Suite 400, Bethesda, MD, USA.
Neuropharmacology. 2022 Nov 1;218:109220. doi: 10.1016/j.neuropharm.2022.109220. Epub 2022 Aug 17.
New medicines containing classic hallucinogenic and entactogenic psychedelic substance are under development for various psychiatric and neurological disorders. Many of these, including psilocybin, lysergic acid diethylamide (LSD), and 3,4-methylenedioxymethamphetamine (MDMA) are Schedule I controlled substances of the United States Controlled Substances Act (US CSA), and similarly controlled globally. The implications of the CSA for research and medicines development, the path to approval of medicines, and their subsequent removal from Schedule I in the US are discussed. This entire process occurs within the framework of the CSA in the US and its counterparts internationally in accordance with international drug control treaties. Abuse potential related research in the US informs the eight factors of the CSA which provide the basis for rescheduling actions that must occur upon approval of a drug that contains a Schedule I substance. Abuse-related research also informs drug product labeling and the risk evaluation and mitigation strategies (REMS) will likely be required for approved medicines. Human abuse potential studies typically employed in CNS drug development may be problematic for substances with strong hallucinogenic effects such as psilocybin, and alternative strategies are discussed. Implications for research, medicinal development, and controlled substance scheduling are presented in the context of the US CSA and FDA requirements with implications for global regulation. We also discuss how abuse-related research can contribute to understanding mechanisms of action and therapeutic effects as well as the totality of the effects of the drugs on the brain, behavior, mood, and the constructs of spirituality and consciousness.
新的含有经典致幻和致瘾性迷幻物质的药物正在开发中,用于治疗各种精神和神经疾病。其中许多药物,包括裸盖菇素、麦角酸二乙酰胺(LSD)和 3,4-亚甲基二氧甲基苯丙胺(MDMA),都是美国管制物质法案(US CSA)的附表 I 管制物质,在全球范围内也受到类似的管制。本文讨论了 CSA 对研究和药物开发的影响、药物获得批准的途径,以及它们在美国从附表 I 中移除的情况。整个过程都是在美国 CSA 及其国际对应物的框架内进行的,符合国际毒品管制条约。美国与滥用相关的研究为 CSA 的八项因素提供了信息,这些因素为含有附表 I 物质的药物获得批准后必须进行重新分类的行动提供了依据。滥用相关的研究还为药物产品标签和风险评估和缓解策略(REMS)提供信息,这些策略很可能是获得批准的药物所必需的。在 CNS 药物开发中通常采用的人类滥用潜力研究可能对具有强烈致幻作用的物质(如裸盖菇素)存在问题,本文讨论了替代策略。本文还讨论了 CSA 和 FDA 要求对研究、药物开发和管制物质分类的影响,以及对全球监管的影响。我们还讨论了与滥用相关的研究如何有助于理解作用机制和治疗效果,以及药物对大脑、行为、情绪以及精神和意识结构的总影响。