Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
2010-022991-29Phase 3Completed
Phase 3, randomised, double-blind trial in opioid-induced bowel dysfunction (OIBD) and functional gastrointestinal disorder (FGID) comparing Lubiprostone 48 mcg/day with Placebo (2 arms). Primary endpoint: Overall spontaneous bowel movement (SBM) response rate. Started Dec 2010; 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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