drugset / Trial / NCT07420283

A Study of Brenipatide in Participants With Opioid Use Disorder

NCT07420283

Phase 2 Recruiting 465 enrolled Eli Lilly and Company
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to see if brenipatide, when compared to placebo, is safe and effective for participants with opioid use disorder, when used with buprenorphine with or without naloxone. The maximum potential duration of study participation for a participant in Part A is approximately 144 weeks, maximum potential duration of study participation for a participant in Part B is approximately 116 weeks. The actual duration will vary for each participant depending on the time of enrollment and the overall rate of study enrollment.

Timeline

Start
2026-02-13
Primary completion
2028-03
Completion
2028-03

Drugs

EvaluationDrugModalityDoseRoute
Subject LY3537031 Unknown Subcutaneous
Background Buprenorphine Other / unclassified Other