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Statistical methodology for the evaluation of vaccine efficacy in a phase III multi-centre trial of the RTS,S/AS01 malaria vaccine in African children

机译:在非洲儿童中进行的RTS,S / AS01疟疾疫苗III期多中心试验中评估疫苗效力的统计方法

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Background There has been much debate about the appropriate statistical methodology for the evaluation of malaria field studies and the challenges in interpreting data arising from these trials. Methods The present paper describes, for a pivotal phase III efficacy of the RTS, S/AS01 malaria vaccine, the methods of the statistical analysis and the rationale for their selection. The methods used to estimate efficacy of the primary course of vaccination, and of a booster dose, in preventing clinical episodes of uncomplicated and severe malaria, and to determine the duration of protection, are described. The interpretation of various measures of efficacy in terms of the potential public health impact of the vaccine is discussed. Conclusions The methodology selected to analyse the clinical trial must be scientifically sound, acceptable to regulatory authorities and meaningful to those responsible for malaria control and public health policy. Trial registration Clinicaltrials.gov NCT00866619
机译:背景技术关于评估疟疾现场研究的适当统计方法以及解释这些试验产生的数据所面临的挑战,一直存在很多争论。方法对于RTS的关键III期疗效,本文描述了S / AS01疟疾疫苗的统计分析方法及其选择的依据。描述了用于估计主要疫苗接种过程和加强剂量在预防简单并发症和严重疟疾的临床发作以及确定保护时间方面的功效的方法。讨论了根据疫苗对公共健康的潜在影响对各种功效度量的解释。结论选择的用于分析临床试验的方法必须科学合理,监管机构可以接受并且对负责疟疾控制和公共卫生政策的人员有意义。试用注册Clinicaltrials.gov NCT00866619

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