Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT03636269Phase 3Completed
Phase 3, randomised, double-blind trial in uremic pruritus comparing CR845 0.5mcg/kg with Placebo (2 arms). Primary endpoint: Reduction of Itch Intensity as Assessed by the Percentage of Patients Achieving an Improvement From Baseline >=3 Points With Respect to the Weekly Mean of the Daily 24-hour Worst Itching Intensity… at 12 weeks. Started Jul 2018; 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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