DRUG
Macupatide
Administered SC
Status
Recruiting
Phase
Phase 2
Enrollment
200
Locations
42
Results
Not posted
Publications
0
Study summary
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
DRUG
Administered SC
DRUG
Administered SC
DRUG
Administered SC
DRUG
Administered SC
Timeline
First posted
Oct 10, 2025
Study start
Oct 16, 2025
Primary completion
Mar 2027
Study completion
May 2027
Results posted
Not reported
Registry updated
Jul 17, 2026
Outcomes
Percent Change from Baseline in Body Weight
Time frame · Baseline, Week 32
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
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
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
No PMID-linked publications were present in this registry snapshot.
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Research pages describe evidence. Vendor pages, where available, describe independently tracked research-product listings and are not clinical recommendations.