Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT04757493Phase 3Unknown
Phase 3, randomised, double-blind trial in irritable bowel syndrome (IBS) comparing Prucalopride Group with Placebo Group (2 arms). Primary endpoints: IBS-Symptom Severity Score at 6 weeks and IBS-Quality of Life at 6 weeks. Status: unknown.
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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