Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT07230418Phase 1Completed
Phase 1, randomised, double-blind trial in chronic spontaneous urticaria (CSU) comparing HRS-3095 Group with HRS-3095 Placebo Group (2 arms). Primary endpoints: Incidence of adverse events at 21 days and Incidence of serious adverse events at 21 days. Started Nov 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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