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A Study to Investigate Weight Management With Macupatide and Eloralintide, Alone or in Combination, in Adult Participants With Obesity or Overweight
RecruitingPhase 2
A Phase 2b, Parallel-Group, Double-Blind, Placebo-Controlled Study to Investigate Weight Management With Macupatide and Eloralintide, Alone or in Combination, in Adult Participants With Obesity or Overweight and Without Type 2 Diabetes
Who can join
Ages 18 to 75 · All sexes
Full eligibility criteria
Inclusion Criteria:
* See Master Protocol CWMM (NCT06143956) for inclusion criteria
Exclusion Criteria:
In addition to exclusion criteria in Master Protocol CWMM (NCT06143956):
* Have type 1 diabetes or type 2 diabetes
* Have an ongoing history of bradyarrhythmia and/or sinus bradycardia
* Have an elevated resting pulse rate (greater than 100 bpm) or reduced resting pulse rate (less than 60 bpm)
* Have a history of acute or chronic pancreatitis
* All concomitant medications should be at a stable dose for at least 3 months prior to screening
About the study
The main purpose of this study, performed under the master protocol W8M-MC-CWMM (NCT06143956), is to examine the body weight-lowering efficacy and safety of macupatide plus eloralintide compared with placebo in participants with obesity or overweight and without type 2 diabetes. Participation will last about 64 weeks.
What is being tested
- Macupatide (drug)
- Eloralintide (drug)
- Placebo (drug)
Sponsor: Eli Lilly and Company · Participants: 400 · Started: May 15, 2026
Contact the study team
- Trial questions or participation questions: 1-877-CTLILLY (1-877-285-4559) or · Phone: 317-615-4559
Official record on ClinicalTrials.gov — NCT07589608
Locations in the U.S.
| Arizona | The Institute for Liver Health II dba Arizona Clinical Trials - Mesa, Chandler Headlands Research - Scottsdale, Scottsdale The Institute for Liver Health II dba Arizona Liver Health-Tucson, Tucson |
| California | NorCal Medical Research, Inc, Greenbrae Velocity Clinical Research, Huntington Park, Huntington Park Peninsula Research Associates, Rolling Hills Estates Diablo Clinical Research, Inc., Walnut Creek |
| Connecticut | Stamford Therapeutics Consortium, Stamford |
| Florida | New Horizon Research Center, Miami Indago Research & Health Center, Inc, Miami Lakes Suncoast Clinical Research, Inc., New Port Richey Charter Research - Winter Park, Orlando Charter Research - Lady Lake, The Villages |
| Idaho | Medical Research Partners, Ammon |
| Illinois | Great Lakes Clinical Trials - Ravenswood, Chicago |
| Kansas | Cotton O'Neil Diabetes & Endocrinology, Topeka |
| Kentucky | Monroe Biomedical Research - Louisville, Louisville |
| Massachusetts | Knownwell, Needham Lucida Clinical Trials, New Bedford |
| Michigan | Headlands Research - Detroit, Southfield Arcturus Healthcare , PLC, Troy Internal Medicine Research Division, Troy |
| Missouri | StudyMetrix Research, City of Saint Peters Clinvest Headlands Llc, Springfield |
| Nevada | Las Vegas Medical Research, Las Vegas |
| New York | Dent Neurologic Institute, Amherst Rochester Clinical Research, LLC, Rochester |
| North Carolina | Medication Management, Greensboro Monroe Biomedical Research, Monroe Lucas Research, Inc, Morehead City Lucas Research, Inc., New Bern |
| Ohio | CTI Clinical Research Center, Cincinnati |
| South Carolina | Tribe Clinical Research, LLC, Greenville |
| Tennessee | Quality Medical Research, Nashville |
| Texas | IMA Clinical Research Austin, Austin FutureSearch Trials of Dallas, Dallas PlanIt Research, PLLC, Houston Endeavor Clinical Trials, San Antonio Texas Valley Clinical Research, Weslaco |
| Virginia | Sovah Clinical Research-River District, Danville |
| Washington | Central Washington Health Services Association d/b/a Confluence Health, Wenatchee |
Conditions
From ClinicalTrials.gov, data retrieved Sep 29, 2026. Each study sets its own eligibility; the study team decides who can join.