通过从人类受试者转移到患者伴侣来创建临床试验社区:每个试验人员都应该问的3个问题

JG Merritt, Tiffany Kuo
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引用次数: 0

摘要

2019冠状病毒病大流行暴露了一个影响我们每个人生计、安全和健康的公共卫生领域。在寻求结束全球疫情的过程中,美国人每天都自愿成为第一个接受安慰剂或新疗法的人,突然之间,我们作为一个社区也被告知临床试验、疫苗安全和开发以及研究设计。随着参与的扩大,建立一个由研究人员、患者和临床医生组成的社区的机会变得成熟,并改变临床研究中历史上被称为“人类受试者”的概念,我们鼓励这种动力,以加强临床研究生态系统,主要关注患者参与共同开发临床研究设计的所有阶段。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Creating a clinical trials community by moving from human subjects to patient partners: 3 questions every trialist should ask
The COVID-19 pandemic has exposed an area of public health impacting the livelihoods, safety, and health of each and every one of us. As everyday Americans volunteered to be first to receive placebo or novel therapeutics in the quest to end a global outbreak, suddenly we as a community were also informed of clinical trials, vaccine safety and development, and research design. As engagement spreads and the opportunity becomes ripe to build a community of researchers, patients, and clinicians and transform what has historically been termed “human subjects” in clinical research, we encourage this drive to strengthen the clinical research ecosystem with a primary focus on patient involvement in all phases of codeveloping clinical research design.
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