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.
All Keywords
【저자키워드】 Vaccine, clinical trial, Immunity, Sample size, severe malaria,
【저자키워드】 Vaccine, clinical trial, Immunity, Sample size, severe malaria,