Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT06939777Phase 2Completed
Phase 2, randomised, double-blind trial of SNA02-48 in Tetanus (12 arms), sponsored by Sinovac Life Sciences. Primary endpoints: Incidence of adverse reactions at 105 days and Increase in serum tetanus antibody levels from baseline at 12 hours post-administration. Started Apr 2025; 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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