Giganti Mark J, Chew Kara W, Moser Carlee, Eron Joseph J, Pinilla Mauricio, Li Jonathan Z, Ritz Justin, Javan Arzhang Cyrus, Wohl David Alain, Daar Eric S, Currier Judith S, Smith Davey M, Hughes Michael D
Harvard T.H. Chan School of Public Health, Boston, MA 02115, USA.
David Geffen School of Medicine at UCLA, Los Angeles, CA 90024, USA.
Contemp Clin Trials. 2025 Jun;153:107887. doi: 10.1016/j.cct.2025.107887. Epub 2025 Mar 25.
Seamless phase 2/3 study designs provide a framework for a more efficient trial. During the COVID-19 pandemic, such study designs were considered particularly appealing as there was an urgent global need to rapidly identify effective therapeutics. However, limited in vivo safety and efficacy data was available early in the pandemic to inform decisions. As part of the ACTIV-2 study, we implemented a phase 2/3 platform trial to evaluate multiple candidate treatments for non-hospitalized adults with COVID-19. In addition to an adequate safety profile, the decision to graduate an agent from phase 2 to phase 3 was based on showing treatment effects on clinical or laboratory markers. Decision criteria evolved over time as more data became available during the global pandemic. A seamless transition and approximately 20 % reduction in total sample size was achieved for one agent, amubarvimab plus romlusevimab. Using both simulation studies and actual results from graduation assessments of five ACTIV-2 candidate therapeutics, we provide a discussion of lessons learned from our implementation and recommendations for future seamless trials of interventions for emergent infections.
无缝衔接的2/3期研究设计为更高效的试验提供了一个框架。在新冠疫情期间,此类研究设计被认为特别有吸引力,因为全球迫切需要迅速确定有效的治疗方法。然而,在疫情早期,体内安全性和有效性数据有限,难以据此做出决策。作为ACTIV-2研究的一部分,我们开展了一项2/3期平台试验,以评估多种针对非住院新冠成年患者的候选治疗方法。除了具备足够的安全性外,将一种药物从2期推进到3期的决定是基于其对临床或实验室指标显示出治疗效果。随着全球疫情期间可获得的数据增多,决策标准也随时间而演变。对于一种药物,即安巴韦单抗联合罗米司韦单抗,实现了无缝过渡且总样本量减少了约20%。利用模拟研究以及ACTIV-2五种候选治疗药物的毕业评估实际结果,我们讨论了从实施过程中吸取的经验教训,并为未来针对新发感染的干预措施无缝试验提出了建议。