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Phase 3Recruiting

A Study of Eloralintide (LY3841136) in Participants With Obesity, or Overweight Without Type 2 Diabetes

Sponsored by Eli Lilly and Company

About this study

The purpose of this study is to evaluate the efficacy and safety of eloralintide in adults with obesity or overweight who do not have type 2 diabetes. The study has two phases: a main phase and an extension phase. Participation in the main phase of the study will last about 75 weeks. Participants with prediabetes will continue in the extension phase for another 2 years.

Where this study is enrolling (36)

  • MFA Clinical Research

    Tuscaloosa, Alabama

    Call 205-331-4963

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  • Headlands Research - Scottsdale

    Scottsdale, Arizona

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  • University Clinical Investigators, Inc.

    Tustin, California

    Call 714-734-7944

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  • Desert Oasis Healthcare Medical Group

    Palm Springs, California

    Call 760-320-9505

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  • Neighborhood Healthcare Institute of Health

    Escondido, California

    Call 760-737-6984

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Show all 36 locations
  • Care Access - Sacramento

    Sacramento, California

    Call 925-734-2331

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  • Ark Clinical Research - Fountain Valley

    Fountain Valley, California

    Call 714-988-2021

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  • Southern California Clinical Research

    Santa Ana, California

    Call 714-474-2173

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  • Peninsula Research Associates

    Rolling Hills Estates, California

    Call 310-265-1623

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  • Chase Medical Research, LLC

    Waterbury, Connecticut

    Call 203-437-6856

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  • Adult Medicine of Lake County, Inc.

    Mt. Dora, Florida

    Call 352-383-8222

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  • American Research Centers of Florida

    Pembroke Pines, Florida

    Call 954-237-3799

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  • BioMed Research & Medical Center

    Miami, Florida

    Call 786-238-7110

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  • JEM Research Institute

    Atlantis, Florida

    Call 561-968-2933

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  • IMA Clinical Research St. Petersburg

    St. Petersburg, Florida

    Call 727-521-9137

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  • AHF Pensacola

    Pensacola, Florida

    Call 850-476-3131 x53026

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  • Teak Research Consults - Dunwoody

    Dunwoody, Georgia

    Call 470-403-4755

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  • Clinical Research Atlanta

    Stockbridge, Georgia

    Call 770-507-6867

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  • East-West Medical Research Institute

    Honolulu, Hawaii

    Call 808-531-6886

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  • Cotton O'Neil Clinical Research Center

    Topeka, Kansas

    Call 785-354-9591

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  • Care Access - Lake Charles (Bayou Pines)

    Lake Charles, Louisiana

    Call 337-602-6642

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  • MedStar Good Samaritan Hospital

    Baltimore, Maryland

    Call 443-444-6275

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  • MedStar Health Research Institute (MedStar Physician Based Research Network)

    Hyattsville, Maryland

    Call 443-444-5663

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  • Care Access - Quincy

    Quincy, Massachusetts

    Call 877-791-0656

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  • Arcturus Healthcare , PLC, Troy Internal Medicine Research Division

    Troy, Michigan

    Call 248-312-0025

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  • AMR Clinical

    Las Vegas, Nevada

    Call 702-597-9825

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  • Albuquerque Clinical Trials, Inc.

    Albuquerque, New Mexico

    Call 505-224-7407

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  • Rochester Clinical Research, LLC

    Rochester, New York

    Call 585-288-0890

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  • Monroe Biomedical Research

    Monroe, North Carolina

    Call 704-283-7359

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  • Preferred Primary Care Physicians

    Uniontown, Pennsylvania

    Call 724-912-0033

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  • Accellacare - Mt Pleasant

    Mt. Pleasant, South Carolina

    Call 843-849-1880

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  • Tribe Clinical Research, LLC

    Greenville, South Carolina

    Call 864-334-0141

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  • AMR Clinical

    Nashville, Tennessee

    Call 630-491-1900

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  • The University of Texas Health Science Center at Houston

    Bellaire, Texas

    Call 713-486-1350

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  • IMA Clinical Research San Antonio

    San Antonio, Texas

    Call 210-692-7157

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  • AMR Clinical

    Norfolk, Virginia

    Call 757-627-7446

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Who can participate

Inclusion criteria

  • ✓Have Body Mass Index (BMI) at screening of the following:
  • ✓30 kilogram per square meter (kg/m2) OR
  • ✓27 kg/m2 with at least one of the following weight-related health conditions at screening:
  • ✓high blood pressure
  • ✓dyslipidemia
  • ✓obstructive sleep apnea, or
  • ✓heart disease
  • ✓Have a stable body weight (\<5% body weight change) for 90 days prior to screening.
  • ✓Have a history of at least one self-reported unsuccessful dietary effort to reduce body weight

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 or type 2 diabetes
  • ✕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
  • ✕Have taken medications or alternative remedies intended for weight loss within 90 days of screening

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.