| Literature DB >> 26768568 |
An Vandebosch1, Robin Mogg2, Nele Goeyvaerts3, Carla Truyers3, Brian Greenwood4, Debby Watson-Jones4, Guillermo Herrera-Taracena5, Wim Parys3, Tony Vangeneugden3.
Abstract
Starting in December 2013, West Africa was overwhelmed with the deadliest outbreak of Ebola virus known to date, resulting in more than 27,500 cases and 11,000 deaths. In response to the epidemic, development of a heterologous prime-boost vaccine regimen was accelerated and involved preparation of a phase 3 effectiveness study. While individually randomized controlled trials are widely acknowledged as the gold standard for demonstrating the efficacy of a candidate vaccine, there was considerable debate on the ethical appropriateness of these designs in the context of an epidemic. A suitable phase 3 trial must convincingly ensure unbiased evaluation with sufficient statistical power. In addition, efficient evaluation of a vaccine candidate is required so that an effective vaccine can be immediately disseminated. This manuscript aims to present the statistical and modeling considerations, design rationale and challenges encountered due to the emergent, epidemic setting that led to the selection of a cluster-randomized phase 3 study design under field conditions.Entities:
Keywords: Ebola; modeling and simulation; phase 3 design; statistical challenges; vaccine efficacy
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Year: 2016 PMID: 26768568 DOI: 10.1177/1740774515621059
Source DB: PubMed Journal: Clin Trials ISSN: 1740-7745 Impact factor: 2.486