A Study of Eloralintide (LY3841136) in Participants With Obesity or Overweight
Part of paid clinical trials in San Antonio, Texas.
- Sponsor
- Eli Lilly and Company
- Study ID
- NCT07738614
- Phase
- PHASE1
- Status
- Recruiting
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 65 Years
- Healthy Volunteers
- Accepted
Interventions
- Eloralintide — DRUGAdministered SC
- Placebo — DRUGAdministered SC
- Acetaminophen — DRUGAdministered Oral Solution
Study Details
The main purpose of this study is to find out how significantly Eloralintide slows stomach emptying in participants who are overweight or obese. For each participant, the study will last approximately 21 weeks and will include 2 overnight stays in the clinical research unit (CRU) lasting between 4 and 8 days. There will be 13 other visits.
Key Dates
- First listed
- Jul 31, 2026
- Start date
- Jul 31, 2026
- Status verified
- Aug 2026
- Primary completion
- Dec 31, 2026
- Completion
- Dec 31, 2026
Study Design
- Enrollment
- 56 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Eloralintide Cohort 1Eloralintide administered subcutaneously (SC)
- Experimental: Eloralintide Cohort 2Eloralintide administered SC
- Experimental: Eloralintide Cohort 3Eloralintide administered SC
- Experimental: Eloralintide Cohort 4Eloralintide administered SC
- Placebo Comparator: PlaceboPlacebo administered SC
Primary Outcome Measure
Acetaminophen Area Under the Concentration Versus Time Curve (AUC) [ Time Frame: Baseline to Day 65 ]
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 |
|---|---|---|---|---|
| ICON Early Phase Services | San Antonio | Texas | 78209 | 210-225-5437 Chinonye Ogbonnaya-Odor (PRINCIPAL_INVESTIGATOR) |
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