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精神疾病的药物研发:精神病学临床试验场所如何应对新冠疫情的挑战。

Drug Development for Mental Illness: How Psychiatry Clinical Trial Sites are Meeting the Challenge of the COVID-19 Pandemic.

作者信息

Litman Robert E, Sorantin Peter, Acevedo-Diaz Elia E

机构信息

Drs. Litman is with CBH Health, Georgetown University Medical School in Washington, DC.

Dr. Sorantin is with Sorantin Outcomes, LLC, in Mountain Lakes, New Jersey.

出版信息

Innov Clin Neurosci. 2021 Jan 1;18(1-3):35-38. eCollection 2021 Jan-Mar.

Abstract

The goal was to review the impact of the COVID-19 pandemic on psychiatric drug development and clinical trials. Disruption of pharmaceutical industry- sponsored clinical trials for psychiatric disorders by the COVID-19 pandemic, prompted by concerns regarding the safety of trial participants and the feasibility of trial conduct, has adversely impacted psychiatric drug development. In response, psychiatry trial sites have modified clinical trials and adapted trial conduct, through the use of social distancing, personal protective equipment, laboratory testing, and remote assessments, to reduce the risks of COVID-19. We review the implications of these modifications for participant safety, safe trial conduct, and data integrity. Given these implications, ongoing communication and consultation are needed between trials sites, sponsors, and all other stakeholders to ensure continued progress in psychiatric drug development during the pandemic.

摘要

目的是评估新冠疫情对精神科药物研发及临床试验的影响。新冠疫情引发了对试验参与者安全性和试验实施可行性的担忧,导致制药行业赞助的精神疾病临床试验中断,对精神科药物研发产生了不利影响。作为应对措施,精神科试验场所通过采取社交距离、个人防护装备、实验室检测和远程评估等手段,对临床试验进行了调整和改进,以降低新冠病毒感染风险。我们将审视这些调整对参与者安全、试验安全实施及数据完整性的影响。鉴于这些影响,试验场所、申办方及所有其他利益相关者之间需要持续沟通与协商,以确保疫情期间精神科药物研发能持续推进。

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