drugset / Trial / NCT07545759

A Study of Brenipatide (LY3537031) in Participants With Irritable Bowel Syndrome-Diarrhea (IBS-D)

NCT07545759 ↗

Phase 2 Recruiting 531 enrolled Eli Lilly and Company
RandomizedParallel-groupDouble-blindTreatment

Summary

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-Diarrhea (IBS-D). The study drug will be administered subcutaneously (SC) (under the skin) when compared with placebo. The study will last approximately 36 weeks.

Timeline

Start
2026-05-06
Primary completion
2027-09
Completion
2027-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Brenipatide Unknown — Subcutaneous