| Literature DB >> 26923455 |
Bronner P Gonçalves1, D Rebecca Prevots2, Edward Kabyemela3, Michal Fried4, Patrick E Duffy5.
Abstract
Severe malaria is a major cause of mortality in children, but comprises only a small proportion of Plasmodium falciparum infections in naturally exposed populations. The evaluation of vaccines that prevent severe falciparum disease will require clinical trials whose primary efficacy endpoint will be severe malaria risk during follow-up. Here, we show that such trials are feasible with fewer than 1000 participants in areas with intense malaria transmission during the age interval when severe malaria incidence peaks. Published by Elsevier Ltd.Entities:
Keywords: Clinical trial; Immunity; Sample size; Severe malaria; Vaccine
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Year: 2016 PMID: 26923455 PMCID: PMC4803582 DOI: 10.1016/j.vaccine.2016.02.053
Source DB: PubMed Journal: Vaccine ISSN: 0264-410X Impact factor: 3.641