University of North Carolina, Chapel Hill, North Carolina (L.L.).
Foundation for the National Institutes of Health, North Bethesda, Maryland (S.J.A.).
Ann Intern Med. 2021 Sep;174(9):1293-1300. doi: 10.7326/M21-1269. Epub 2021 Jun 29.
Working in an unprecedented time frame, the Accelerating COVID-19 Therapeutic Interventions and Vaccines (ACTIV) public-private partnership developed and launched 9 master protocols between 14 April 2020 and 31 May 2021 to allow for the coordinated and efficient evaluation of multiple investigational therapeutic agents for COVID-19. The ACTIV master protocols were designed with a portfolio approach to serve the following patient populations with COVID-19: mild to moderately ill outpatients, moderately ill inpatients, and critically ill inpatients. To facilitate the execution of these studies and minimize start-up time, ACTIV selected several existing networks to launch the master protocols. The master protocols were also designed to test several agent classes prioritized by ACTIV that covered the spectrum of the disease pathophysiology. Each protocol, either adaptive or pragmatic, was designed to efficiently select those treatments that provide benefit to patients while rapidly eliminating those that were either ineffective or unsafe. The ACTIV Therapeutics-Clinical Working Group members describe the process by which these master protocols were designed, developed, and launched. Lessons learned that may be useful in meeting the challenges of a future pandemic are also described.
在一个前所未有的时间框架内,加速 COVID-19 治疗干预和疫苗(ACTIV)公私合作伙伴关系开发并推出了 9 个主方案,从 2020 年 4 月 14 日至 2021 年 5 月 31 日,以允许对多种 COVID-19 研究治疗药物进行协调和有效的评估。ACTIV 主方案采用投资组合方法设计,为以下 COVID-19 患者人群提供服务:轻度至中度门诊患者、中度住院患者和重症住院患者。为了促进这些研究的执行并最小化启动时间,ACTIV 选择了几个现有的网络来启动主方案。主方案还旨在测试 ACTIV 优先考虑的几种药物类别,这些类别涵盖了疾病病理生理学的范围。每个协议,无论是适应性的还是务实的,都旨在有效地选择那些对患者有益的治疗方法,同时迅速淘汰那些无效或不安全的治疗方法。ACTIV 治疗学-临床工作组的成员描述了这些主方案的设计、开发和推出的过程。还描述了在应对未来大流行的挑战方面可能有用的经验教训。