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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 failure

About 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

Sponsor: Eli Lilly and Company · Participants: 900 · Started: Feb 10, 2026

Contact the study team

Official record on ClinicalTrials.gov — NCT07392190

Locations in the U.S.

AlabamaBirmingham Clinical Research, Birmingham
ArizonaRIO Clinical Trials - Phoenix, Phoenix
Headlands Research - Scottsdale, Scottsdale
Novak Clinical Research - Tucson - North La Cholla Boulevard, Tucson
CaliforniaIrvine 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
ConnecticutNew England Research Associates, LLC, Bridgeport
Yale University School of Medicine, New Haven
Chase Medical Research, LLC, Waterbury
FloridaJEM 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
GeorgiaTeak Research Consults - Dunwoody, Dunwoody
Center for Advanced Research & Education, Gainesville
Clinical Research Atlanta, Stockbridge
IdahoFamily First Medical Center, Idaho Falls
IllinoisGreat Lakes Clinical Trials - Ravenswood, Chicago
IowaIowa Diabetes and Endocrinology Research Center, West Des Moines
KansasCotton O'Neil Diabetes & Endocrinology, Topeka
KentuckyAMR Clinical, Lexington
LouisianaIMA Clinical Research Monroe - Armand, Monroe
MarylandCentennial Medical Group, Columbia
MassachusettsBrigham and Women's Hospital Diabetes Program, Boston
MedVadis Research Corporation, Waltham
MichiganGreat Lakes Research Institute, Southfield
Revive Research Institute, Inc., Southfield
Arcturus Healthcare , PLC, Troy Internal Medicine Research Division, Troy
MissouriClinical Research Professionals, Chesterfield
New YorkIMA Clinical Research Manhattan, New York
NYU Langone Health, New York
Weill Cornell Medical College, New York
North CarolinaUniversity of North Carolina Medical Center, Chapel Hill
Medication Management, Greensboro
Carteret Medical Group, Morehead City
Accellacare - Wilmington - 1917 Tradd Court, Wilmington
OhioCTI Clinical Research Center, Cincinnati
Care Access - Lima, Lima
PennsylvaniaPreferred Primary Care Physicians, Preferred Clinical Research (Ofc 18), Pittsburgh
South CarolinaTrial Management Associates, Myrtle Beach (Not yet recruiting)
TexasUT 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.