Current partner codePEPTIDESDE
NCT07215559·Phase 2·INTERVENTIONAL

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

Status

Recruiting

Phase

Phase 2

Enrollment

200

Locations

42

Results

Not posted

Publications

0

Study summary

What the protocol is testing.

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.

Interventions

Treatment arms and agents.

DRUG

Macupatide

Administered SC

DRUG

Eloralintide

Administered SC

DRUG

Macupatide Placebo

Administered SC

DRUG

Eloralintide Placebo

Administered SC

Timeline

From registration to results.

  1. First posted

    Oct 10, 2025

  2. Study start

    Oct 16, 2025

  3. Primary completion

    Mar 2027

  4. Study completion

    May 2027

  5. Results posted

    Not reported

  6. Registry updated

    Jul 17, 2026

Outcomes

What the study measures.

Primary outcomes

Percent Change from Baseline in Body Weight

Time frame · Baseline, Week 32

Secondary outcomes

Change from Baseline in Hemoglobin A1c (HbA1c)

Time frame · Baseline, Week 32

Change from Baseline in Body Mass Index (BMI)

Time frame · Baseline, Week 32

Change from Baseline in Fasting Glucose

Time frame · Baseline, Week 32

Eligibility

Who can take part.

Minimum age
18 Years
Maximum age
75 Years
Sex
ALL
Healthy volunteers
No

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

Study locations

42 registered sites.

Argentina · Australia · Puerto Rico · United States. Showing up to 24 locations stored in the fast local snapshot.

Prime Medical Group, LLC dba Gilbert Center for Family Medicine, LLC

Gilbert, Arizona, United States

Synexus Clinical Research US, Inc.

Phoenix, Arizona, United States

Pima Heart

Tucson, Arizona, United States

Precision Clinical Research

Sunrise, Florida, United States

SKY Clinical Research Network Group-Brown

Atlanta, Georgia, United States

Teak Research Consults

Lawrenceville, Georgia, United States

AGILE Clinical Research Trials, LLC

Sandy Springs, Georgia, United States

Pivotal Research Solutions

Stonecrest, Georgia, United States

Rophe Adult and Pediatric Medicine/SKYCRNG

Union City, Georgia, United States

Vector Clinical Trials

Las Vegas, Nevada, United States

Premier Research

Trenton, New Jersey, United States

PriMED Clinical Research

Dayton, Ohio, United States

Mercy Family Clinic

Dallas, Texas, United States

Velocity Clinical Research, Dallas

Dallas, Texas, United States

Biopharma Informatic, LLC

Houston, Texas, United States

PlanIt Research, PLLC

Houston, Texas, United States

Research Physicians Network, LLC

Houston, Texas, United States

Aavon Clinical Trials

Richmond, Texas, United States

Consano Clinical Research, LLC

Shavano Park, Texas, United States

Texas Valley Clinical Research

Weslaco, Texas, United States

Kalo Clinical Research

West Valley City, Utah, United States

Eastern Virginia Medical School (EVMS) Medical Group

Norfolk, Virginia, United States

Clinical Research Partners, LLC

Richmond, Virginia, United States

Northwest Clinical Research Center

Bellevue, Washington, United States

Publications

Results and literature.

No PMID-linked publications were present in this registry snapshot.

Primary links

Continue at the source.

Related trials

More studies on Eloralintide.

Related PeptideStat pages

Put the record in context.

Research pages describe evidence. Vendor pages, where available, describe independently tracked research-product listings and are not clinical recommendations.