Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT06530966Phase 1Completed
Phase 1, randomised, double-blind trial comparing ICP-332 with Placebo (2 arms). Primary endpoints: Number of participants with Adverse Events at 28 days, Number of Participants With Clinically Significant Change in Vital Signs at 28 days and 3 more. Started Jul 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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