澳大利亚故事:致幻剂临床应用的现状和未来挑战。

IF 6.8 2区 医学 Q1 PHARMACOLOGY & PHARMACY
David J Nutt, Peter Hunt, Anne Katrin Schlag, Paul Fitzgerald
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引用次数: 0

摘要

在过去的十年里,迷幻药和3,4-亚甲基二氧甲基苯丙胺(MDMA)的临床研究有了巨大的增长,它们显示出治疗精神疾病的巨大潜力。鉴于这一研究进展,以及目前数百万患者未满足的临床需求,澳大利亚药品管理局(TGA)于2023年批准将裸盖菇素用于治疗难治性抑郁症,将MDMA用于治疗创伤后应激障碍,从2023年7月1日起生效。TGA批准运动由澳大利亚慈善机构澳大利亚精神医学联盟领导,得到了来自莫纳什大学的David Nutt教授、药物科学教授、Arthur Christopolous教授、Chris Langmead教授以及大量临床、学术和患者团体的支持。根据重新安排,目前的处方权仅限于根据TGA的授权处方者计划成为授权处方者的精神科医生,并且裸盖菇素只能用于治疗难治性抑郁症,MDMA只能用于治疗创伤后应激障碍。本文回顾了这一决定的背景,其对其他司法管辖区批准的影响,以及其他致幻剂的发展途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Australia story: Current status and future challenges for the clinical applications of psychedelics.

The past decade has seen a huge increase in clinical research with psychedelic drugs and 3,4-methylenedioxymethamphetamine (MDMA), which have revealed great potential for treating mental health conditions. Given this progress in research, as well as the current unmet clinical need of millions of patients, in 2023, the Australian Therapeutic Goods Administration (TGA) approved the use of psilocybin for treatment-resistant depression and MDMA for PTSD to take effect from 1 July 2023. The campaign for TGA approval was led by a coalition comprising the Australian charity Mind Medicine Australia with support from Professor David Nutt, Drug Science, Professor Arthur Christopolous, Professor Chris Langmead (both from Monash University) and from large numbers of clinical, academic and patient groups. Under the rescheduling, current prescribing rights are limited to psychiatrists who have become authorised prescribers under the TGA's Authorised Prescriber Scheme, and psilocybin can only be used for treatment resistant depression and MDMA can only be used for PTSD. This paper reviews the background for this decision, its implications for approvals in other jurisdictions, as well as for the development pathways for other psychedelic drugs.

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来源期刊
CiteScore
15.40
自引率
12.30%
发文量
270
审稿时长
2.0 months
期刊介绍: The British Journal of Pharmacology (BJP) is a biomedical science journal offering comprehensive international coverage of experimental and translational pharmacology. It publishes original research, authoritative reviews, mini reviews, systematic reviews, meta-analyses, databases, letters to the Editor, and commentaries. Review articles, databases, systematic reviews, and meta-analyses are typically commissioned, but unsolicited contributions are also considered, either as standalone papers or part of themed issues. In addition to basic science research, BJP features translational pharmacology research, including proof-of-concept and early mechanistic studies in humans. While it generally does not publish first-in-man phase I studies or phase IIb, III, or IV studies, exceptions may be made under certain circumstances, particularly if results are combined with preclinical studies.
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