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Phase 3Recruiting

A Study of Eloralintide (LY3841136) in Participants With Persistent Obesity Who Are Treated With a Weekly Incretin

Sponsored by Eli Lilly and Company

About this study

The main purpose of this study is to evaluate the efficacy and safety of eloralintide compared with placebo in participants with persistent obesity or overweight, with or without type 2 diabetes, and on stable incretin background therapy. Participation in the study will last about 80 weeks.

Where this study is enrolling (51)

  • Birmingham Clinical Research

    Birmingham, Alabama

    Call 205-870-4343

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  • Novak Clinical Research - Tucson - North La Cholla Boulevard

    Tucson, Arizona

    I'm interested
  • Headlands Research - Scottsdale

    Scottsdale, Arizona

    I'm interested
  • RIO Clinical Trials - Phoenix

    Phoenix, Arizona

    I'm interested
  • Artemis Institute for Clinical Research

    San Diego, California

    Call 858-278-3647

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Show all 51 locations
  • Care Access - Sacramento

    Sacramento, California

    Call 925-734-2331

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  • Southern California Clinical Research

    Santa Ana, California

    Call 714-474-2173

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  • Scripps Whittier Diabetes Institute

    La Jolla, California

    Call 858-824-5352

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  • Peninsula Research Associates

    Rolling Hills Estates, California

    Call 310-265-1623

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  • Irvine Clinical Research

    Irvine, California

    Call 949-753-1663

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  • University Clinical Investigators, Inc.

    Tustin, California

    Call 714-734-7944

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  • EndoTrials Center for Clinical Research

    La Mesa, California

    Call 619-460-2626

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  • New England Research Associates, LLC

    Bridgeport, Connecticut

    Call 203-374-9816

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  • Chase Medical Research, LLC

    Waterbury, Connecticut

    Call 203-419-4420

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  • Yale University School of Medicine

    New Haven, Connecticut

    Call 203-785-7421

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  • JEM Research Institute

    Atlantis, Florida

    Call 561-968-2933

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  • St Johns Center for Clinical Research

    Saint Augustine, Florida

    Call 904-209-0043

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  • Northeast Research Institute (NERI)

    Fleming Island, Florida

    Call 904-541-8225

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  • New Horizon Research Center

    Miami, Florida

    Call 305-226-3933

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  • Jacksonville Center for Clinical Research

    Jacksonville, Florida

    Call 904-730-0101

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  • Metabolic Research Institute, Inc.

    West Palm Beach, Florida

    Call 561-802-3060

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  • Teak Research Consults - Dunwoody

    Dunwoody, Georgia

    Call 470-403-4755

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  • Center for Advanced Research & Education

    Gainesville, Georgia

    Call 770-534-5154

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  • Clinical Research Atlanta

    Stockbridge, Georgia

    Call 770-507-6867

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  • Family First Medical Center

    Idaho Falls, Idaho

    Call 208-552-7700

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  • Great Lakes Clinical Trials - Ravenswood

    Chicago, Illinois

    I'm interested
  • Cotton O'Neil Diabetes & Endocrinology

    Topeka, Kansas

    Call 785-354-9591

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  • Centennial Medical Group

    Columbia, Maryland

    Call 410-730-3399

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  • Brigham and Women's Hospital Diabetes Program

    Boston, Massachusetts

    Call 617-732-4245

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  • MedVadis Research Corporation

    Waltham, Massachusetts

    Call 617-744-1310

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  • Great Lakes Research Institute

    Southfield, Michigan

    Call 248-864-5242

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  • Revive Research Institute, Inc.

    Southfield, Michigan

    Call 248-829-3103

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  • Arcturus Healthcare , PLC, Troy Internal Medicine Research Division

    Troy, Michigan

    Call 248-312-0025

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  • Clinical Research Professionals

    Chesterfield, Missouri

    Call 636-220-1200

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  • NYU Langone Health

    New York, New York

    Call 212-263-3166

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  • Weill Cornell Medical College

    New York, New York

    Call 646-962-2111

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  • Medication Management

    Greensboro, North Carolina

    Call 336-763-6968

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  • Carteret Medical Group

    Morehead City, North Carolina

    Call 252-499-8623

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  • Accellacare - Wilmington - 1917 Tradd Court

    Wilmington, North Carolina

    Call 910-799-5500

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  • University of North Carolina Medical Center

    Chapel Hill, North Carolina

    Call 984-974-3004

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  • CTI Clinical Research Center

    Cincinnati, Ohio

    Call 513-721-3868

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  • Preferred Primary Care Physicians, Preferred Clinical Research (Ofc 18)

    Pittsburgh, Pennsylvania

    Call 412-650-6155

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  • Trial Management Associates

    Myrtle Beach, South Carolina

    Call 843-994-7655

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  • Activian Clinical Research

    Kingwood, Texas

    Call 832-969-3401

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  • Texas Valley Clinical Research

    Weslaco, Texas

    Call 956-431-8090

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  • Juno Research

    Houston, Texas

    Call (713) 779-5494

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  • Medrasa Clinical Research

    Wylie, Texas

    Call 469-449-3645

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  • Consano Clinical Research, LLC

    Shavano Park, Texas

    Call 210-545-4900

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  • Endeavor Clinical Trials

    San Antonio, Texas

    Call 518-428-6859

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  • IMA Clinical Research San Antonio

    San Antonio, Texas

    Call 210-692-7157

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  • Synergy Groups Medical LLC - Missouri City

    Missouri City, Texas

    Call 832-532-4210

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Who can participate

Inclusion criteria

  • ✓Are on stable incretin therapy at screening
  • ✓With persistent obesity or overweight defined as:
  • ✓≥30 kg/m2 OR
  • ✓≥27 kg/m2 with at least one existing obesity related complication at screening:
  • ✓hypertension
  • ✓dyslipidemia
  • ✓obstructive sleep apnea
  • ✓cardiovascular disease (for example, ischemic cardiovascular disease, New York Heart Association Functional Class I-III heart failure), or
  • ✓type 2 diabetes
  • ✓Have a stable body weight (\<5% body weight change) at screening

Exclusion criteria

  • ✕Have a prior or planned surgical treatment for obesity (liposuction, cryolipolysis, or abdominoplasty allowed if performed \>1 year before screening)
  • ✕Have a prior or planned endoscopic procedure and/or device-based therapy for obesity (prior device-based therapy acceptable if device removal was more than 6 months prior to screening)
  • ✕Have type 1 diabetes
  • ✕Have taken any of the following antihyperglycemic medications within 90 days before screening:
  • ✕dipeptidyl peptidase-4 (DPP-4) inhibitors
  • ✕amylin analogs
  • ✕insulin
  • ✕Have had within 90 days prior to screening:
  • ✕heart attack
  • ✕stroke
  • ✕coronary artery revascularization
  • ✕unstable angina, or
  • ✕hospitalization due to congestive heart failure
  • ✕Have a history or diagnosis of New York Heart Association Functional Classification Class IV congestive heart failure

Only the research team can confirm whether you qualify. The intake questionnaire is the best way to find out.

Completing a questionnaire on Clinably does not enroll you in a clinical trial or confirm your eligibility. Only the research team can determine whether you qualify to participate. These results are based on the information you provide and are intended to help you start a conversation with the research team.

Trial data sourced from ClinicalTrials.gov.