Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT03883620Phase 1Completed
Phase 1, randomised, single-blind trial of VIS513 in dengue fever (7 cohorts), sponsored by Serum Institute of India. Primary endpoints: Proportion of participants with post-injection/infusion adverse events at 4 hours, Proportion of participants with AEs, discontinuations due to AEs, and serious adverse events at 84 days and 1 more. Started Mar 2019; status: completed.
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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