A Study of LY3841136 Compared With Placebo in Adult Participants With Obesity or Overweight

August 27, 2025 updated by: Eli Lilly and Company

A Phase 2, Parallel-Group, Double-Blind Study to Investigate Weight Management With LY3841136 Compared With Placebo in Adult Participants With Obesity or Overweight

The main purpose of this study, performed under the master protocol W8M-MC-CWMM (NCT06143956), is to investigate weight management efficacy and safety with LY3841136 compared with placebo in adult participants with obesity or overweight. The study will last about 64 weeks and may include up to 17 visits.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

263

Phase

  • Phase 2

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Argentina
      • Buenos Aires, Argentina, C1056ABI
        • Centro de Investigaciones Metabólicas (CINME)
    • Buenos Aires F.D.
      • Buenos Aires, Buenos Aires F.D., Argentina, C1120AAC
        • Centro Médico Viamonte
      • Buenos Aires, Buenos Aires F.D., Argentina, C1425AGC
        • Centro Medico Dra. Laura Maffei- Investigacion Clinica Aplicada
  • United States
    • Arizona
      • Chandler, Arizona, United States, 85225
        • The Institute for Liver Health II dba Arizona Clinical Trials - Mesa
      • Scottsdale, Arizona, United States, 85260
        • Headlands Research - Scottsdale
      • Tucson, Arizona, United States, 85712
        • The Institute for Liver Health II dba Arizona Liver Health-Tucson
    • California
      • Greenbrae, California, United States, 94904
        • NorCal Medical Research, Inc
      • Huntington Park, California, United States, 90255
        • Velocity Clinical Research, Huntington Park
      • Rolling Hills Estates, California, United States, 90274
        • Peninsula Research Associates
      • Walnut Creek, California, United States, 94598
        • Diablo Clinical Research, Inc.
    • Florida
      • Fleming Island, Florida, United States, 32003
        • Northeast Research Institute (NERI)
      • New Port Richey, Florida, United States, 34652
        • Suncoast Clinical Research, Inc.
      • Orlando, Florida, United States, 32803
        • Charter Research - Winter Park
      • The Villages, Florida, United States, 32162
        • Charter Research - Lady Lake
    • Hawaii
      • Honolulu, Hawaii, United States, 96817
        • Pacific Diabetes & Endocrine Center
    • Idaho
      • Ammon, Idaho, United States, 83406
        • Medical Research Partners
    • Illinois
      • Chicago, Illinois, United States, 60640
        • Great Lakes Clinical Trials - Andersonville
      • Chicago, Illinois, United States, 60640
        • Great Lakes Clinical Trials - Ravenswood
      • Skokie, Illinois, United States, 60077
        • Northshore University Health System
    • Iowa
      • West Des Moines, Iowa, United States, 50265
        • Iowa Diabetes and Endocrinology Research Center
    • Kansas
      • Topeka, Kansas, United States, 66606
        • Cotton O'Neil Diabetes & Endocrinology
    • Kentucky
      • Louisville, Kentucky, United States, 40213
        • L-MARC Research Center
    • Massachusetts
      • Needham, Massachusetts, United States, 02492
        • Knownwell
      • New Bedford, Massachusetts, United States, 02740
        • Lucida Clinical Trials
    • Michigan
      • Southfield, Michigan, United States, 48034
        • Headlands Research - Detroit
      • Troy, Michigan, United States, 48098
        • Arcturus Healthcare , PLC, Troy Internal Medicine Research Division
    • Missouri
      • City of Saint Peters, Missouri, United States, 63303
        • StudyMetrix Research
    • Nevada
      • Las Vegas, Nevada, United States, 89128
        • Las Vegas Medical Research
    • New York
      • Amherst, New York, United States, 14226
        • Dent Neurologic Institute
      • East Syracuse, New York, United States, 13057
        • Velocity Clinical Research, Syracuse
      • Port Jefferson Station, New York, United States, 11776
        • North Suffolk Neurology
      • Rochester, New York, United States, 14609
        • Rochester Clinical Research, LLC
    • North Carolina
      • Greensboro, North Carolina, United States, 27405
        • Medication Management
      • Monroe, North Carolina, United States, 28112
        • Monroe Biomedical Research
      • New Bern, North Carolina, United States, 28562
        • Lucas Research, Inc.
    • Ohio
      • Cincinnati, Ohio, United States, 45212
        • CTI Clinical Research Center
    • South Carolina
      • Greenville, South Carolina, United States, 29607
        • Tribe Clinical Research, LLC
    • Tennessee
      • Nashville, Tennessee, United States, 37211
        • Quality Medical Research
    • Texas
      • Austin, Texas, United States, 78745
        • IMA Clinical Research Austin
      • Dallas, Texas, United States, 75230
        • Velocity Clinical Research, Dallas
      • Dallas, Texas, United States, 75251
        • FutureSearch Trials of Dallas
      • Houston, Texas, United States, 77079
        • PlanIt Research, PLLC
      • San Antonio, Texas, United States, 78240
        • Endeavor Clinical Trials
      • San Antonio, Texas, United States, 78229
        • Tekton Research - Fredericksburg Road
    • Virginia
      • Danville, Virginia, United States, 24541
        • Spectrum Medical, Inc.
    • Washington
      • Wenatchee, Washington, United States, 98801
        • Central Washington Health Services Association d/b/a Confluence Health

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

W8M-MC-LAA1

  • Are males and females who agree to abide by the reproductive and contraceptive requirements

W8M-MC-CWMM:

  • Have a BMI ≥27 kg/m²
  • Have had a stable body weight for the 3 months prior to randomization (<5% body weight gain and/or loss)

Exclusion Criteria:

W8M-MC-LAA1

  • Have any prior diagnosis 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).
  • Have a history of acute or chronic pancreatitis.
  • Have an on-going or history of bradyarrhythmia and/or sinus bradycardia at screening and baseline.

W8M-MC-CWMM

  • Have a prior or planned surgical treatment for obesity, except prior liposuction or abdominoplasty, if performed >1 year prior to screening.
  • Have type 1 diabetes mellitus, latent autoimmune diabetes in adults, or history of ketoacidosis or hyperosmolar coma.
  • Have poorly controlled hypertension.
  • Have a history of symptomatic gallbladder disease within the past 2 years
  • Have signs and symptoms of any liver disease other than nonalcoholic fatty liver disease.
  • Have a lifetime history of suicide attempts.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: LY3841136 Dose 4
Participants will receive LY3841136 SC.
Drug: LY3841136
Administered SC.
Experimental: LY3841136 Dose 1
Participants will receive LY3841136 subcutaneously (SC)
Drug: LY3841136
Administered SC.
Experimental: LY3841136 Dose 2
Participants will receive LY3841136 SC
Drug: LY3841136
Administered SC.
Experimental: LY3841136 Dose 3
Participants will receive LY3841136 SC
Drug: LY3841136
Administered SC.
Experimental: LY3841136 Dose 5
Participants will receive LY3841136 SC
Drug: LY3841136
Administered SC.
Experimental: LY3841136 Dose 6
Participants will receive LY3841136 SC
Drug: LY3841136
Administered SC.
Placebo Comparator: Placebo
Participants will receive LY3841136 matching placebo
Drug: Placebo
Administered SC.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Percent Change from Baseline in Body Weight
Time Frame: Baseline, Week 48
Baseline, Week 48

Secondary Outcome Measures

Outcome Measure
Time Frame
Change from Baseline in Body Weight
Time Frame: Baseline, Week 48
Baseline, Week 48
Percentage of Participants Who Achieve ≥5% Body Weight Reduction
Time Frame: Baseline to Week 48
Baseline to Week 48
Percentage of Participants Who Achieve ≥10% Body Weight Reduction
Time Frame: Baseline to Week 48
Baseline to Week 48
Change from Baseline in Body Mass Index (BMI)
Time Frame: Baseline, Week 48
Baseline, Week 48
Pharmacokinetics (PK): Area Under the Curve (AUC) of LY3841136
Time Frame: Baseline to Week 48
Baseline to Week 48
PK: Maximum Concentration (Cmax) of LY3841136
Time Frame: Baseline to Week 48
Baseline to Week 48

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Eli Lilly and Company

Investigators

  • Study Director: Call 1-877-CTLILLY (1-877-285-4559) or 1-317-615-4559 Mon - Fri 9 AM - 5 PM Eastern time (UTC/GMT - 5 hours, EST), Eli Lilly and Company

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Helpful Links

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

February 5, 2024

Primary Completion (Actual)

May 30, 2025

Study Completion (Actual)

August 14, 2025

Study Registration Dates

First Submitted

January 21, 2024

First Submitted That Met QC Criteria

January 21, 2024

First Posted (Actual)

January 30, 2024

Study Record Updates

Last Update Posted (Estimated)

August 28, 2025

Last Update Submitted That Met QC Criteria

August 27, 2025

Last Verified

August 1, 2025

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 18808
  • CWMM Master Protocol (Other Identifier: Eli Lilly and Company)
  • W8M-MC-LAA1 (Other Identifier: Eli Lilly and Company)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

Anonymized individual patient level data will be provided in a secure access environment upon approval of a research proposal and a signed data sharing agreement.

IPD Sharing Time Frame

Data are available 6 months after the primary publication and approval of the indication studied in the US and EU, whichever is later. Data will be indefinitely available for requesting.

IPD Sharing Access Criteria

A research proposal must be approved by an independent review panel and researchers must sign a data sharing agreement.

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL
  • SAP
  • CSR

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

Yes

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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