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A Study of Macupatide (LY3532226) and Eloralintide (LY3841136), Alone or in Combination, in Adults With Obesity or Overweight and With Type 2 Diabetes

RecruitingPhase 2

A Phase 2, Parallel-Group, Double-Blind, Placebo-Controlled Study to Investigate Weight Reduction With Macupatide and Eloralintide, Alone or in Combination, in Adult Participants With Obesity or Overweight and With Type 2 Diabetes

Who can join

Ages 18 to 75 · All sexes

Full eligibility criteria
Inclusion Criteria:

* Have type 2 diabetes
* Have an HbA1c ≥7.5% to ≤10.5% at screening
* Have been treated with any of the following, alone or in combination, for at least 3 months prior to screening

  * Diet and exercise
  * Stable dose of metformin
  * Sodium-glucose cotransporter-2 (SGLT2) inhibitor
* Have had a stable body weight (\<5% body weight gain and/or loss) for the 3 months prior to screening
* Have a BMI of 27 or greater at screening

Exclusion Criteria:

* Have any form of diabetes other than type 2 diabetes
* Have a prior or planned surgical treatment for obesity, except prior liposuction or abdominoplasty, if performed \>1 year prior to screening
* Have any of the following cardiovascular conditions within 3 months prior to screening:

  * acute myocardial infarction
  * cerebrovascular accident (stroke)
  * unstable angina, or
  * hospitalization due to congestive heart failure
* Have a history of an active or untreated malignancy or are in remission from a clinically significant malignancy for less than 5 years, exceptions include

  * basal or squamous cell skin cancer
  * in situ carcinomas of the cervix, or
  * in situ prostate cancer
* Have been prescribed any of the following receptor agonists (RA) or their combination for any indication within the last 6 months:

  * amylin RA
  * dual amylin and calcitonin RA
  * glucagon-like peptide-1 receptor (GLP-1) RA
  * glucose-dependent insulinotropic peptide (GIP)/GLP-1 RA
  * GLP-1/glucagon (GCG) RAs, or
  * GIP/GLP-1/GCG RAs
* Have used excluded antihyperglycemic medications within 3 months prior to screening (including, but not limited to, sulfonylureas, dipeptidyl peptidase-4 inhibitors, alpha-glucosidase inhibitors, thiazolidinediones, and meglitinides
* Have used insulin for diabetic control within the prior year (short term use in certain situations allowed

About the study

The purpose of this study is to investigate weight reduction with macupatide and eloralintide, alone or in combination, in adult participants with obesity or overweight and with type 2 diabetes. Participation in the study will last about 48 weeks.

What is being tested

Sponsor: Eli Lilly and Company · Participants: 200 · Started: Oct 16, 2025

Contact the study team

Official record on ClinicalTrials.gov — NCT07215559

Locations in the U.S.

ArizonaPrime Medical Group, LLC dba Gilbert Center for Family Medicine, LLC, Gilbert
Synexus Clinical Research US, Inc., Phoenix
Pima Heart, Tucson
FloridaPrecision Clinical Research, Sunrise
GeorgiaSKY Clinical Research Network Group-Brown, Atlanta
Teak Research Consults, Lawrenceville
AGILE Clinical Research Trials, LLC, Sandy Springs
Pivotal Research Solutions, Stonecrest
Rophe Adult and Pediatric Medicine/SKYCRNG, Union City
NevadaVector Clinical Trials, Las Vegas
New JerseyPremier Research, Trenton
OhioPriMED Clinical Research, Dayton
TexasMercy Family Clinic, Dallas
Velocity Clinical Research, Dallas, Dallas
Biopharma Informatic, LLC, Houston
PlanIt Research, PLLC, Houston
Research Physicians Network, LLC, Houston
Aavon Clinical Trials, Richmond
Consano Clinical Research, LLC, Shavano Park
Texas Valley Clinical Research, Weslaco
UtahKalo Clinical Research, West Valley City
VirginiaEastern Virginia Medical School (EVMS) Medical Group, Norfolk
Clinical Research Partners, LLC, Richmond
WashingtonNorthwest Clinical Research Center, Bellevue
Rainier Clinical Research Center, Renton
Universal Research Group, Tacoma

Conditions

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.