Current and Future Challenges in Trial Design for Pre-Exposure Prophylaxis in HIV Prevention

D. Donnell
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引用次数: 3

Abstract

Abstract Success in establishing efficacy of antiretroviral drugs to prevent acquisition of HIV infection has fundamentally changed the trial design considerations for future experimental drugs. Current trials of potential new antiretroviral agents for pre-exposure prophylaxis are using active control designs – where all trial participants receive an active antiretroviral drug. Current trials of other experimental approaches, such as vaccines and monoclonal antibodies, permit use of the proven prevention agent FTC/TDF for all trial participants. In the future, if even more effective prevention methods are approved, active control designs would anticipate very few infection events and not provide statistically robust evidence. A potential alternative is to conduct placebo randomized trials limited to participants for whom current prevention tools are not acceptable.
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HIV预防暴露前预防试验设计的当前和未来挑战
成功确立抗逆转录病毒药物预防获得性HIV感染的疗效,从根本上改变了未来实验药物的试验设计考虑。目前针对潜在的用于暴露前预防的新型抗逆转录病毒药物的试验采用了主动对照设计,即所有试验参与者都接受一种有效的抗逆转录病毒药物。目前对其他实验方法(如疫苗和单克隆抗体)的试验允许对所有试验参与者使用经证实的预防剂FTC/TDF。在未来,如果更有效的预防方法得到批准,主动控制设计将预测很少的感染事件,并且不能提供统计上可靠的证据。一个潜在的替代方案是进行安慰剂随机试验,限制在目前的预防工具不能接受的参与者中。
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Study design approaches for future active-controlled HIV prevention trials. The role of randomization inference in unraveling individual treatment effects in early phase vaccine trials. Nonlinear mixed-effects models for HIV viral load trajectories before and after antiretroviral therapy interruption, incorporating left censoring. Estimation and interpretation of vaccine efficacy in COVID-19 randomized clinical trials Sample size calculation for active-arm trial with counterfactual incidence based on recency assay.
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