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Taking people in United StatesPhase 2

A Study of Brenipatide (LY3537031) in Participants With Irritable Bowel Syndrome-Constipation (IBS-C)

Key facts

Where
Anaheim, Columbus, Hollywood, Lancaster, Los Alamitos, Louisville, McAllen, Mesa, New Albany, New York, Providence, San Antonio, Springfield, and Webster, United StatesSee the 14 sites
Phase
Phase 2

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 75 years old?

Source: NCT07545772, who can take part

Where in United States

  • Smart Cures Clinical ResearchAnaheim, United StatesContact: Dennis Riff (principal investigator)Taking people
  • Ohio GastroenterologyColumbus, United StatesContact: Ryan Gaible (principal investigator)Taking people
  • Encore Medical ResearchHollywood, United StatesContact: Rodolfo Perez (principal investigator)Taking people
  • Om Research LLCLancaster, United StatesContact: Jatinder Pruthi (principal investigator)Taking people
  • United Medical Doctors - Los AlamitosLos Alamitos, United StatesContact: Seyedehsan Navabi (principal investigator)Taking people
  • Gastroenterology Health PartnersLouisville, United StatesContact: Michael Krease (principal investigator)Taking people
  • Biopharma Informatic, LLCMcAllen, United StatesContact: Ralph Alhalel, MD (principal investigator)Taking people
  • Del Sol Research Management - MesaMesa, United StatesContact: David Tessler (principal investigator)Taking people
  • Gastroenterology Health PartnersNew Albany, United StatesContact: Jonathan Obert (principal investigator)Taking people
  • New York Gastroenterology AssociatesNew York, United StatesContact: Yevgenia Pashinsky (principal investigator)Taking people
  • University GastroenterologyProvidence, United StatesContact: Lisa Mueller (principal investigator)Taking people
  • Southern Star Research InstituteSan Antonio, United StatesContact: Jeff Bullock (principal investigator)Taking people
  • Springfield Clinic - FirstSpringfield, United StatesContact: Rajan Kochar (principal investigator)Taking people
  • GI Alliance WebsterWebster, United StatesContact: Sudhanshu Gogia (principal investigator)Taking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

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Trial details

Who runs it
Eli Lilly and Company
Trial code
NCT07545772EU 2025-524974-41-00
Record updated
5 November 2026
Original description
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.Read full original descriptionShow less

A Phase 2, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of Brenipatide in the Treatment of Adult Participants With IBS-C

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 36 weeks.

Inclusion: Meets Rome IV criteria for irritable bowel syndrome-constipation (IBS-C) including having more than 25% bowel movements with Bristol Stool Form Scale (BSFS) Types 1 or 2 and less than 25% of bowel movements with BSFS Types 6 or 7; Based on the daily eDiary collection during the screening period:; Have average of worst abdominal pain score of ≥3.0 on a 0-to-10-point scale during the 14 consecutive days prior to randomization.

Exclusion: Have a diagnosis of irritable bowel syndrome (IBS) with a subtype of diarrhea, mixed IBS, or unclassified IBS by the Rome IV criteria; Have a history of inflammatory or immune-mediated gastrointestinal disorders; Have a known clinically significant gastric emptying abnormality.

ClinicalTrials.gov NCT07545772 · EU CTIS 2025-524974-41-00