Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT00139672Phase 2Completed
Phase 2, randomised, double-blind trial in irritable bowel syndrome (IBS) comparing PD-217,014 with Placebo (2 arms). Primary endpoint: Relief of abdominal pain/discomfort responder rate at 4 weeks. Started Jan 2004; 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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