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Clinical Trials in Australia / NCT07215559
Recruiting Phase 2

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

NCT07215559 · tracked via the Priya Life Science Australia tracker
Phase
Phase 2
Started
2025-10-16
Last updated
2026-09-08

Condition(s) studied

ObesityOverweightDiabetes Mellitus, Type 2

Investigational drug(s) / intervention(s)

Macupatide →Eloralintide →Macupatide PlaceboEloralintide Placebo

Macupatide: Administered SC

Eloralintide: Administered SC

Macupatide Placebo: Administered SC

Eloralintide Placebo: Administered SC

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.

Eligibility

Sex
ALL
Min age
18 Years
Max age
75 Years
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

Primary outcome measure(s)

Trial sites (42)

FacilityCityRegionStatus
Prime Medical Group, LLC dba Gilbert Center for Family Medicine, LLC Gilbert Arizona Recruiting
Synexus Clinical Research US, Inc. Phoenix Arizona Recruiting
Pima Heart Tucson Arizona Recruiting
Precision Clinical Research Sunrise Florida Recruiting
SKY Clinical Research Network Group-Brown Atlanta Georgia Recruiting
Teak Research Consults Lawrenceville Georgia Recruiting
AGILE Clinical Research Trials, LLC Sandy Springs Georgia Recruiting
Pivotal Research Solutions Stonecrest Georgia Recruiting
Rophe Adult and Pediatric Medicine/SKYCRNG Union City Georgia Recruiting
Vector Clinical Trials Las Vegas Nevada Recruiting
Premier Research Trenton New Jersey Recruiting
PriMED Clinical Research Dayton Ohio Recruiting
Mercy Family Clinic Dallas Texas Recruiting
Velocity Clinical Research, Dallas Dallas Texas Recruiting
Biopharma Informatic, LLC Houston Texas Recruiting
PlanIt Research, PLLC Houston Texas Recruiting
Research Physicians Network, LLC Houston Texas Recruiting
Aavon Clinical Trials Richmond Texas Recruiting
Consano Clinical Research, LLC Shavano Park Texas Recruiting
Texas Valley Clinical Research Weslaco Texas Recruiting
Kalo Clinical Research West Valley City Utah Recruiting
Eastern Virginia Medical School (EVMS) Medical Group Norfolk Virginia Recruiting
Clinical Research Partners, LLC Richmond Virginia Recruiting
Northwest Clinical Research Center Bellevue Washington Recruiting
Rainier Clinical Research Center Renton Washington Recruiting
Universal Research Group Tacoma Washington Recruiting
Centro de Investigaciones Metabólicas (CINME) Buenos Aires Argentina Recruiting
CENUDIAB Buenos Aires Argentina Recruiting
CEDIC CABA Argentina Recruiting
Instituto de Investigaciones Clínicas Córdoba Córdoba Argentina Recruiting
Clínica Universitaria Reina Fabiola Córdoba Argentina Recruiting
Go Centro Medico San Nicolás San Nicolás Argentina Recruiting
Emeritus Research Botany Australia Recruiting
Core Research Group Brisbane Australia Recruiting
Emeritus Research Camberwell Australia Recruiting
Cornerstone Dermatology Coorparoo Australia Recruiting
Momentum Darlinghurst Darlinghurst, Sydney Australia Recruiting
CDH Research Institute Pty Ltd Maroochydore Australia Recruiting
Momentum Sunshine Melbourne Australia Recruiting
AIM Research Merewether Australia Completed

+ 2 more sites — see the full list on the official registry below.

More Eli Lilly and Company trials in Australia

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07215559 on ClinicalTrials.gov ↗ ← All trials in Australia