Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT06937593Phase 1Completed
Phase 1, randomised, double-blind trial of VIS-954 (4 arms), sponsored by Otsuka Pharmaceutical Development & Commercialization. Primary endpoints: Incidence of treatment-emergent adverse events at 169 days, Maximum serum concentration at 169 days and 1 more. Started Mar 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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