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.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
531
Percentage of Participants Who Had a Daily Composite Response for at Least 50 Percent (%) of Days
Time frame: Week 9 to Week 16
Percentage of Participants Who Had a Daily Abdominal Pain Response for at Least 50% of Days
Time frame: Week 9 to Week 16
Percentage of Participants Who Had Daily Stool Consistency Response for at Least 50% of Days
Time frame: Week 1 to Week 24
Percentage of Participants Who Had a Daily Composite Response
Time frame: Day 1 through Week 24
Trial questions or participation questions: 1-877-CTLILLY (1-877-285-4559) or
CONTACT
Physicians interested in becoming principal investigators please contact
CONTACT
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