A Study of Brenipatide (LY3537031) in Healthy Participants With Overweight or Obesity
Part of paid clinical trials in Daytona Beach, Florida.
- Sponsor
- Eli Lilly and Company
- Study ID
- NCT07476118
- Phase
- PHASE1
- Status
- Recruiting
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 65 Years
- Healthy Volunteers
- Accepted
Interventions
- Brenipatide — DRUGAdministered SC.
- Placebo — OTHERAdministered SC.
Study Details
The main purpose of this study is to evaluate how different dose levels of brenipatide work and how safe they are in healthy people with overweight or obesity. The study will assess the effects of different doses given as subcutaneous (under the skin) injections. Participation in this study will last about 42 weeks.
Key Dates
- Start date
- Mar 18, 2026
- Status verified
- Apr 2026
- Primary completion
- Feb 28, 2027
- Completion
- Feb 28, 2027
Study Design
- Enrollment
- 150 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- BASIC_SCIENCE
Arms
- Experimental: BrenipatideParticipants will receive brenipatide subcutaneously (SC).
- Placebo Comparator: PlaceboParticipants will receive placebo administered SC.
Primary Outcome Measure
Percent Change in Body Weight [ Time Frame: Week 1, Week 29 ]
Central Contacts
- Trial questions or participation questions: 1-877-CTLILLY (1-877-285-4559)1-317-615-4559
- Physicians interested in becoming principal investigators please contact
Locations (3)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Fortrea Clinical Research Unit - Daytona Beach | Daytona Beach | Florida | 32117-5116 | 866-429-3700 Kathleen Doisy (PRINCIPAL_INVESTIGATOR) |
| Fortrea Clinical Research Unit | Dallas | Texas | 75247 | 866-429-3700 Gene Voskuhl (PRINCIPAL_INVESTIGATOR) |
| Fortrea Clinical Research Unit Inc. - Madison | Madison | Wisconsin | 53704 | 866-429-3700 Kimberly Cruz (PRINCIPAL_INVESTIGATOR) |
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