A Study of LY4167586 in Participants With Obesity or Overweight Who Are Otherwise Healthy
Part of paid clinical trials in Madison, Wisconsin.
- Sponsor
- Eli Lilly and Company
- Study ID
- NCT07225556
- Phase
- PHASE1
- Status
- Recruiting
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 65 Years
- Healthy Volunteers
- Accepted
Interventions
- LY4167586 — DRUGAdministered SC
- Placebo — DRUGAdministered SC
- LY4167586 — DRUGAdministered IV
Study Details
The purpose of this study is to look at how safe and well-tolerated LY4167586 is in participants with obesity or overweight who are otherwise healthy. Blood tests will be performed to check how much LY4167586 gets into the bloodstream and how long it takes the body to eliminate it following a single administration. Participation in the study will last approximately 7 months.
Key Dates
- Start date
- Nov 18, 2025
- Status verified
- Mar 2026
- Primary completion
- Dec 31, 2026
- Completion
- Dec 31, 2026
Study Design
- Enrollment
- 84 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- BASIC_SCIENCE
Arms
- Experimental: LY4167586 (Cohorts A1 to A6)LY4167586 administered subcutaneously (SC)
- Placebo Comparator: LY4167586 (Cohorts A1 to A6) PlaceboLY4167586 administered SC
- Experimental: LY4167586 (Cohort B)LY4167586 administered intravenously (IV)
Primary Outcome Measure
Number and Incidence of Serious Adverse Events (SAEs) [ Time Frame: Baseline to study completion (up to 29 weeks) ]
Central Contacts
- Trial questions or participation questions: 1-877-CTLILLY (1-877-285-4559) or1-317-615-4559
- Physicians interested in becoming principal investigators please contact
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Fortrea Clinical Research Unit | Madison | Wisconsin | 53704 | 866-429-3700 Kimberly Cruz (PRINCIPAL_INVESTIGATOR) |
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