Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT03857568Phase 1Completed
Phase 1, randomised, double-blind trial in pruritus comparing SHR0410 group with Placebo (2 arms). Primary endpoints: Incidence of Adverse events in terms of changes in Hematology at 14 days, Incidence of Adverse events in terms of changes in Urinalysis at 14 days and 2 more. Started Apr 2019; 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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