NCT06124807CompletedPhase 2
A Study of LY3305677 Compared With Placebo in Adult Participants With Obesity or Overweight
A Phase 2, Parallel-Group, Double-Blind, 4-Arm Study to Investigate Weight Management With LY3305677 Compared With Placebo and in Adult Participants With Obesity or Overweight
Source: ClinicalTrials.gov · Last updated 21 Apr 2026
Brief summary (registry, in English)
The main purpose of this study, performed under a master protocol W8M-MC-CWMM (NCT06143956), is to investigate weight management efficacy and safety with Mazdutide compared with placebo and in adult participants with obesity or overweight. The study will last about 62 weeks.
- Status (registry)
- Completed
- Phase (registry)
- Phase 2
- Study type
- Interventional
- Enrollment
- 179 (actual)
- First submitted
- 6 Nov 2023
- Start date
- 17 Nov 2023
- Primary completion date
- 22 Jan 2025
- Lead sponsor
- Eli Lilly and Company
- Diseases
- Obesity
- NCT number
- NCT06124807
What you commit to
- Study type: Interventional · Phase 2
- Participants enrolled: 179
- From 17 Nov 2023 to the primary completion date, 22 Jan 2025
- 29 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Have any prior diagnosis of diabetes mellitus, that is type 2 diabetes mellitus (T2DM), or rare forms of diabetes mellitus, except gestational diabetes.
- Have any of the following cardiovascular conditions within 6 months prior to screening:
- acute myocardial infarction
- cerebrovascular accident (stroke)
- unstable angina, or
- hospitalization due to congestive heart failure (CHF).
- Participants with hypertension who do not have well-controlled blood pressure (BP) (\>140/90 mmHg), regardless of antihypertensive treatment. Participants receiving treatment for hypertension should be on a stable antihypertensive regimen for at least 3 months prior to screening.
- Have a prior or planned surgical treatment for obesity, except prior liposuction or abdominoplasty, if performed \>1 year prior to screening.
Other illness
- Have a history of New York Heart Association (NYHA) Functional Classification I-IV CHF.
- Have a history of acute or chronic pancreatitis.
- Note: If the investigator anticipates a need to add antihypertensive medication during the study, the participant should not be included in the ambulatory blood pressure monitoring (ABPM) procedures.
- CWMM:
- Have type 1 diabetes mellitus, latent autoimmune diabetes in adults, or history of ketoacidosis or hyperosmolar coma.
- Have poorly controlled hypertension.
- Have signs and symptoms of any liver disease other than nonalcoholic fatty liver disease.
- Have a history of symptomatic gallbladder disease within the past 2 years.
- Have a lifetime history of suicide attempts.
Other
- W8M-MC-OXA1:
Who the study is looking for
- W8M-MC-OXA1:
- Are males and females who agree to abide by the reproductive and contraceptive requirements
- W8M-MC-CWMM:
- Have a BMI ≥27 kilograms per square meter (kg/m²)
Age in the registry: 18 years to 75 years · Sex: All · Does not accept healthy volunteers
Sites (29)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Dent Neurologic Institute Coordinator of this site? Confirm its status | Amherst | United States | Unknown status |
| IMA Clinical Research Austin Coordinator of this site? Confirm its status | Austin | United States | Unknown status |
| The Institute for Liver Health II dba Arizona Clinical Trials - Mesa Coordinator of this site? Confirm its status | Chandler | United States | Unknown status |
| Great Lakes Clinical Trials - Ravenswood Coordinator of this site? Confirm its status | Chicago | United States | Unknown status |
| Great Lakes Clinical Trials - Andersonville Coordinator of this site? Confirm its status | Chicago | United States | Unknown status |
| CTI Clinical Research Center Coordinator of this site? Confirm its status | Cincinnati | United States | Unknown status |
| StudyMetrix Research Coordinator of this site? Confirm its status | City of Saint Peters | United States | Unknown status |
| Velocity Clinical Research, Dallas Coordinator of this site? Confirm its status | Dallas | United States | Unknown status |
| Spectrum Medical, Inc. Coordinator of this site? Confirm its status | Danville | United States | Unknown status |
| Northeast Research Institute (NERI) Coordinator of this site? Confirm its status | Fleming Island | United States | Unknown status |
| Pacific Diabetes & Endocrine Center Coordinator of this site? Confirm its status | Honolulu | United States | Unknown status |
| PlanIt Research, PLLC Coordinator of this site? Confirm its status | Houston | United States | Unknown status |
| Velocity Clinical Research-Huntington Park Coordinator of this site? Confirm its status | Huntington Park | United States | Unknown status |
| Las Vegas Medical Research Coordinator of this site? Confirm its status | Las Vegas | United States | Unknown status |
| L-MARC Research Center Coordinator of this site? Confirm its status | Louisville | United States | Unknown status |
| Quality Medical Research Coordinator of this site? Confirm its status | Nashville | United States | Unknown status |
| Knownwell Coordinator of this site? Confirm its status | Needham | United States | Unknown status |
| Lucas Research, Inc. Coordinator of this site? Confirm its status | New Bern | United States | Unknown status |
| Suncoast Clinical Research, Inc. Coordinator of this site? Confirm its status | New Port Richey | United States | Unknown status |
| Charter Research - Winter Park Coordinator of this site? Confirm its status | Orlando | United States | Unknown status |
| North Suffolk Neurology Coordinator of this site? Confirm its status | Port Jefferson Station | United States | Unknown status |
| Peninsula Research Associates Coordinator of this site? Confirm its status | Rolling Hills Estates | United States | Unknown status |
| Tekton Research - Fredericksburg Road Coordinator of this site? Confirm its status | San Antonio | United States | Unknown status |
| Headlands Research - Scottsdale Coordinator of this site? Confirm its status | Scottsdale | United States | Unknown status |
| Charter Research - Lady Lake Coordinator of this site? Confirm its status | The Villages | United States | Unknown status |
| Cotton O'Neil Diabetes & Endocrinology Coordinator of this site? Confirm its status | Topeka | United States | Unknown status |
| The Institute for Liver Health II dba Arizona Liver Health-Tucson Coordinator of this site? Confirm its status | Tucson | United States | Unknown status |
| Diablo Clinical Research, Inc. Coordinator of this site? Confirm its status | Walnut Creek | United States | Unknown status |
| Central Washington Health Services Association d/b/a Confluence Health Coordinator of this site? Confirm its status | Wenatchee | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.