Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT07507838Phase 1Recruiting
Phase 1, randomised, double-blind trial of VV913 (4 arms), sponsored by Vigonvita Life Sciences. Primary endpoints: Incidence of Treatment-Emergent Adverse Events at 6 days, Maximum Observed Plasma Concentration at 72 hours and 9 more. Started Apr 2026; status: 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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