Epidemiology Unit, Health Research Institute-Fundación Jiménez Díaz University Hospital, Universidad Autónoma de Madrid, Madrid, Spain.
The Desmond Tutu HIV Centre, University of Cape Town, Cape Town, South Africa.
Lancet Infect Dis. 2021 Nov;21(11):e342-e347. doi: 10.1016/S1473-3099(21)00263-2. Epub 2021 May 18.
Large-scale deployment of COVID-19 vaccines will seriously affect the ongoing phases 2 and 3 randomised placebo-controlled trials assessing SARS-CoV-2 vaccine candidates. The effect will be particularly acute in high-income countries where the entire adult or older population could be vaccinated by late 2021. Regrettably, only a small proportion of the population in many low-income and middle-income countries will have access to available vaccines. Sponsors of COVID-19 vaccine candidates currently in phase 2 or initiating phase 3 trials in 2021 should consider continuing the research in countries with limited affordability and availability of COVID-19 vaccines. Several ethical principles must be implemented to ensure the equitable, non-exploitative, and respectful conduct of trials in resource-poor settings. Once sufficient knowledge on the immunogenicity response to COVID-19 vaccines is acquired, non-inferiority immunogenicity trials-comparing the immune response of a vaccine candidate to that of an authorised vaccine-would probably be the most common trial design. Until then, placebo-controlled, double-blind, crossover trials will continue to play a role in the development of new vaccine candidates. WHO or the Council for International Organizations of Medical Sciences should define an ethical framework for the requirements and benefits for trial participants and host communities in resource-poor settings that should require commitment from all vaccine candidate sponsors from high-income countries.
大规模部署 COVID-19 疫苗将严重影响正在进行的评估 SARS-CoV-2 疫苗候选物的 2 期和 3 期随机安慰剂对照试验。在高收入国家,这种影响尤其严重,这些国家的所有成年人或老年人都可能在 2021 年底前接种疫苗。遗憾的是,许多低收入和中等收入国家的人口中只有一小部分能够获得现有疫苗。目前处于 2 期或在 2021 年开始 3 期试验的 COVID-19 疫苗候选物的赞助商应考虑在 COVID-19 疫苗供应有限且负担能力有限的国家继续开展研究。必须实施若干伦理原则,以确保在资源匮乏环境中公平、非剥削性和尊重性地开展试验。一旦获得关于 COVID-19 疫苗免疫原性反应的足够知识,非劣效性免疫原性试验(比较疫苗候选物的免疫反应与已授权疫苗的免疫反应)可能将成为最常见的试验设计。在此之前,安慰剂对照、双盲、交叉试验将继续在新疫苗候选物的开发中发挥作用。世界卫生组织或国际医学组织理事会应为资源匮乏环境中试验参与者和宿主社区的要求和获益制定伦理框架,这应要求所有来自高收入国家的疫苗候选物赞助商做出承诺。