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The current recommendation for treating Lassa fever with ribavirin is supported only by weak evidence. Given the persistent effects in areas with endemic transmission and epidemic potential, there is an urgent need to reassess ribavirin and investigate other potential therapeutic candidates; however, a robust clinical trial method adapted to Lassa fever epidemiology has not yet been established. We propose an adaptive phase II/III multicenter randomized controlled platform trial that uses a superiority framework with an equal allocation ratio and accounts for challenges selecting the primary end point and estimating the target sample size by using an interim analysis.

Original publication

DOI

10.3201/eid3102.240251

Type

Journal

Emerging infectious diseases

Publication Date

02/2025

Volume

31

Pages

9 - 16

Keywords

WALC Work Package 2 Working Group, Humans, Lassa virus, Lassa Fever, Ribavirin, Antiviral Agents, Research Design, Clinical Trials, Phase II as Topic, Clinical Trials, Phase III as Topic