Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT06724978Phase 1Completed
Phase 1, randomised trial of S-740792 (3 arms), sponsored by Shionogi & Co., Ltd. Primary endpoints: Treatment-emergent Adverse Events at 28 days, Plasma Concentration of S-740792 at 144 hours and 1 more. Started Nov 2024; 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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