Practical considerations in the establishment of psychedelic research programs.

IF 3.5 3区 医学 Q2 NEUROSCIENCES
Psychopharmacology Pub Date : 2025-01-01 Epub Date: 2024-12-04 DOI:10.1007/s00213-024-06722-6
Brian S Barnett, M Frances Vest, Marcus S Delatte, Franklin King Iv, Erin E Mauney, Anthony J Coulson, Sandeep M Nayak, Peter S Hendricks, George R Greer, Kevin S Murnane
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引用次数: 0

Abstract

Rationale: There is increasing interest in establishing psychedelic research programs at academic medical centers. However, psychedelics are intensely psychoactive, carry considerable sociopolitical baggage, and most are Schedule I drugs, creating significant potential impediments to implementation. There is little formal guidance for investigators on navigating the complex on-the-ground obstacles associated with establishing psychedelic research programs.

Objectives: This article provides recommendations that may be helpful to investigators seeking to work with psychedelics, with a focus on academic medical centers in the United States.

Methods: The academic literature on relevant matters is reviewed, and the authors provide observations from their experiences either working for relevant regulatory agencies or conducting basic science studies, investigator-initiated trials, or industry sponsored trials with psychedelics.

Results: Investigators planning to conduct psychedelic research should cultivate broad institutional support early. Challenges related to securing funding, obtaining approval for an Investigational New Drug application from the Food and Drug Administration, clinical grade drug sourcing, obtaining a Schedule I researcher registration from the Drug Enforcement Administration and an equivalent state license (if required), preparing spaces for treatment and study drug storage, managing controlled substance inventory, engaging the local community, and other issues should be anticipated.

Conclusions: Investigators should anticipate several implementation challenges when planning to work with psychedelics. However, these are likely surmountable with planning, persistence, and assistance from colleagues and other experts.

建立致幻剂研究项目的实际考虑。
理由:在学术医学中心建立致幻剂研究项目的兴趣越来越大。然而,致幻剂具有强烈的精神活性,带有相当大的社会政治包袱,而且大多数是附表1药物,对实施造成了重大的潜在障碍。在建立致幻剂研究项目时,很少有正式的指导来指导研究人员如何克服复杂的实地障碍。目的:这篇文章提供了一些建议,可能有助于研究者寻求与致幻剂的工作,重点是在美国的学术医疗中心。方法:对相关学术文献进行回顾,作者根据自己在相关监管机构工作或进行基础科学研究、研究者发起的试验或行业赞助的迷幻药试验的经验提供观察。结果:计划开展致幻剂研究的研究者应及早培养广泛的机构支持。预计将面临以下挑战:获得资金、获得食品和药物管理局批准的研究新药申请、临床级药物采购、从药品执法管理局获得附表I研究人员注册和等效的州许可证(如果需要)、为治疗和研究药物储存准备空间、管理管制物质库存、参与当地社区和其他问题。结论:研究人员在计划使用致幻剂时应该预料到几个实施方面的挑战。然而,只要有计划、坚持不懈以及同事和其他专家的帮助,这些都是可以克服的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Psychopharmacology
Psychopharmacology 医学-精神病学
CiteScore
7.10
自引率
5.90%
发文量
257
审稿时长
2-4 weeks
期刊介绍: Official Journal of the European Behavioural Pharmacology Society (EBPS) Psychopharmacology is an international journal that covers the broad topic of elucidating mechanisms by which drugs affect behavior. The scope of the journal encompasses the following fields: Human Psychopharmacology: Experimental This section includes manuscripts describing the effects of drugs on mood, behavior, cognition and physiology in humans. The journal encourages submissions that involve brain imaging, genetics, neuroendocrinology, and developmental topics. Usually manuscripts in this section describe studies conducted under controlled conditions, but occasionally descriptive or observational studies are also considered. Human Psychopharmacology: Clinical and Translational This section comprises studies addressing the broad intersection of drugs and psychiatric illness. This includes not only clinical trials and studies of drug usage and metabolism, drug surveillance, and pharmacoepidemiology, but also work utilizing the entire range of clinically relevant methodologies, including neuroimaging, pharmacogenetics, cognitive science, biomarkers, and others. Work directed toward the translation of preclinical to clinical knowledge is especially encouraged. The key feature of submissions to this section is that they involve a focus on clinical aspects. Preclinical psychopharmacology: Behavioral and Neural This section considers reports on the effects of compounds with defined chemical structures on any aspect of behavior, in particular when correlated with neurochemical effects, in species other than humans. Manuscripts containing neuroscientific techniques in combination with behavior are welcome. We encourage reports of studies that provide insight into the mechanisms of drug action, at the behavioral and molecular levels. Preclinical Psychopharmacology: Translational This section considers manuscripts that enhance the confidence in a central mechanism that could be of therapeutic value for psychiatric or neurological patients, using disease-relevant preclinical models and tests, or that report on preclinical manipulations and challenges that have the potential to be translated to the clinic. Studies aiming at the refinement of preclinical models based upon clinical findings (back-translation) will also be considered. The journal particularly encourages submissions that integrate measures of target tissue exposure, activity on the molecular target and/or modulation of the targeted biochemical pathways. Preclinical Psychopharmacology: Molecular, Genetic and Epigenetic This section focuses on the molecular and cellular actions of neuropharmacological agents / drugs, and the identification / validation of drug targets affecting the CNS in health and disease. We particularly encourage studies that provide insight into the mechanisms of drug action at the molecular level. Manuscripts containing evidence for genetic or epigenetic effects on neurochemistry or behavior are welcome.
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