ClinicaliQ Trial Snapshot
- A Study of Brenipatide (LY3537031) in Participants With Irritable Bowel Syndrome-Constipation (IBS-C) — Recruiting • Phase II • Dermatology • NCT07545772.
- Brenipatide injections tested against placebo in patients with constipation-type irritable bowel syndrome over 35 weeks for safety and effectiveness.
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What This Trial Is Studying
The purpose of this study is to evaluate how well brenipatide (LY3537031) is tolerated what side effects may occur, and the safety and efficacy in participants with Irritable Bowel Syndrome-Constipation (IBS-C). The study drug will be administered subcutaneously (SC) (under the skin) when compared with placebo. The study will last approximately 35 weeks. Conditions: Irritable Bowel Syndrome, Constipation Interventions: LY3537031, Placebo Lead Sponsor: Eli Lilly and Company Planned Enrollment: 342 participants