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
Eli Lilly and Company
Summary
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.
Eligibility
- Age range
- 18–75 years
- Sex
- All
- Healthy volunteers
- No
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
Interventions
- DrugMacupatide
Administered SC
- DrugEloralintide
Administered SC
- DrugPlacebo
Administered SC
Locations (40)
- The Institute for Liver Health II dba Arizona Clinical Trials - MesaChandler, Arizona
- Headlands Research - ScottsdaleScottsdale, Arizona
- The Institute for Liver Health II dba Arizona Liver Health-TucsonTucson, Arizona
- NorCal Medical Research, IncGreenbrae, California
- Velocity Clinical Research, Huntington ParkHuntington Park, California
- Peninsula Research AssociatesRolling Hills Estates, California