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A Study of Eloralintide (LY3841136) in Participants With Persistent Obesity Who Are Treated With a Weekly Incretin
RecruitingPhase 3
A Phase 3 Randomized, Double-Blind, Placebo-Controlled Study to Investigate the Efficacy and Safety of Once Weekly Eloralintide in Adult Participants With Persistent Obesity or Overweight Treated With a Weekly Incretin, With and Without Type 2 Diabetes
Who can join
Ages 18 and older · All sexes
Full eligibility criteria
Inclusion Criteria:
* Are on stable incretin therapy at screening
* With persistent obesity or overweight defined as:
* ≥30 kg/m2 OR
* ≥27 kg/m2 with at least one existing obesity related complication at screening:
* hypertension
* dyslipidemia
* obstructive sleep apnea
* cardiovascular disease (for example, ischemic cardiovascular disease, New York Heart Association Functional Class I-III heart failure), or
* type 2 diabetes
* Have a stable body weight (\<5% body weight change) at screening
Exclusion Criteria:
* Have a prior or planned surgical treatment for obesity (liposuction, cryolipolysis, or abdominoplasty allowed if performed \>1 year before screening)
* Have a prior or planned endoscopic procedure and/or device-based therapy for obesity (prior device-based therapy acceptable if device removal was more than 6 months prior to screening)
* Have type 1 diabetes
* Have taken any of the following antihyperglycemic medications within 90 days before screening:
* dipeptidyl peptidase-4 (DPP-4) inhibitors
* amylin analogs
* insulin
* Have had within 90 days prior to screening:
* heart attack
* stroke
* coronary artery revascularization
* unstable angina, or
* hospitalization due to congestive heart failure
* Have a history or diagnosis of New York Heart Association Functional Classification Class IV congestive heart failureAbout the study
The main purpose of this study is to evaluate the efficacy and safety of eloralintide compared with placebo in participants with persistent obesity or overweight, with or without type 2 diabetes, and on stable incretin background therapy.
Participation in the study will last about 80 weeks.
What is being tested
- Eloralintide (drug)
- Placebo (drug)
Sponsor: Eli Lilly and Company · Participants: 900 · Started: Feb 10, 2026
Contact the study team
- Trial questions or participation questions: 1-877-CTLILLY (1-877-285-4559) or · Phone: 317-615-4559
Official record on ClinicalTrials.gov — NCT07392190
Locations in the U.S.
| Alabama | Birmingham Clinical Research, Birmingham |
| Arizona | RIO Clinical Trials - Phoenix, Phoenix Headlands Research - Scottsdale, Scottsdale Novak Clinical Research - Tucson - North La Cholla Boulevard, Tucson |
| California | Irvine Clinical Research, Irvine Scripps Whittier Diabetes Institute, La Jolla EndoTrials Center for Clinical Research, La Mesa (Not yet recruiting) Peninsula Research Associates, Rolling Hills Estates Care Access - Sacramento, Sacramento (Not yet recruiting) Artemis Institute for Clinical Research, San Diego Southern California Clinical Research, Santa Ana University Clinical Investigators, Inc., Tustin |
| Connecticut | New England Research Associates, LLC, Bridgeport Yale University School of Medicine, New Haven Chase Medical Research, LLC, Waterbury |
| Florida | JEM Research Institute, Atlantis AMR Clinical, Doral Northeast Research Institute (NERI), Fleming Island Jacksonville Center for Clinical Research, Jacksonville New Horizon Research Center, Miami St Johns Center for Clinical Research, Saint Augustine Metabolic Research Institute, Inc., West Palm Beach |
| Georgia | Teak Research Consults - Dunwoody, Dunwoody Center for Advanced Research & Education, Gainesville Clinical Research Atlanta, Stockbridge |
| Idaho | Family First Medical Center, Idaho Falls |
| Illinois | Great Lakes Clinical Trials - Ravenswood, Chicago |
| Iowa | Iowa Diabetes and Endocrinology Research Center, West Des Moines |
| Kansas | Cotton O'Neil Diabetes & Endocrinology, Topeka |
| Kentucky | AMR Clinical, Lexington |
| Louisiana | IMA Clinical Research Monroe - Armand, Monroe |
| Maryland | Centennial Medical Group, Columbia |
| Massachusetts | Brigham and Women's Hospital Diabetes Program, Boston MedVadis Research Corporation, Waltham |
| Michigan | Great Lakes Research Institute, Southfield Revive Research Institute, Inc., Southfield Arcturus Healthcare , PLC, Troy Internal Medicine Research Division, Troy |
| Missouri | Clinical Research Professionals, Chesterfield |
| New York | IMA Clinical Research Manhattan, New York NYU Langone Health, New York Weill Cornell Medical College, New York |
| North Carolina | University of North Carolina Medical Center, Chapel Hill Medication Management, Greensboro Carteret Medical Group, Morehead City Accellacare - Wilmington - 1917 Tradd Court, Wilmington |
| Ohio | CTI Clinical Research Center, Cincinnati Care Access - Lima, Lima |
| Pennsylvania | Preferred Primary Care Physicians, Preferred Clinical Research (Ofc 18), Pittsburgh |
| South Carolina | Trial Management Associates, Myrtle Beach (Not yet recruiting) |
| Texas | UT Southwestern Medical Center, Dallas Juno Research, Houston Activian Clinical Research, Kingwood Texas Valley Clinical Research (TVCR) - Mission, Mission Synergy Groups Medical LLC - Missouri City, Missouri City Endeavor Clinical Trials, San Antonio IMA Clinical Research San Antonio, San Antonio Consano Clinical Research, LLC, Shavano Park Texas Valley Clinical Research, Weslaco Medrasa Clinical Research, Wylie |
Conditions
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.