Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT07172724Phase 1Not yet recruiting
Phase 1, randomised, double-blind trial of Vivaxin in Plasmodium vivax malaria (4 arms), sponsored by Universidade Federal de Minas Gerais. Primary endpoints: Safety and reactogenicity of adverse events (AE) in the first 14 days, Safety and reactogenicity of EA in the first 28 days and 2 more. Planned start Sep 2025; status: not yet recruiting.
Beyond the preview
Study design, results and competitive context are available in the Gosset platform where reported.
Available in the Gosset platform where reported.
Available in the Gosset platform where reported.
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