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 35 weeks.
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Percentage of Participants Who Had a Daily Composite Response for at Least 50 Percent (%) of Days
Timeframe: Week 9 to Week 16
Trial questions or participation questions: 1-877-CTLILLY (1-877-285-4559) or