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)
- Call 205-331-4963
MFA Clinical Research
Tuscaloosa, Alabama
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- I'm interested
Headlands Research - Scottsdale
Scottsdale, Arizona
- Call 714-734-7944
University Clinical Investigators, Inc.
Tustin, California
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- Call 760-320-9505
Desert Oasis Healthcare Medical Group
Palm Springs, California
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- Call 760-737-6984
Neighborhood Healthcare Institute of Health
Escondido, California
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Show all 36 locations
- Call 925-734-2331
Care Access - Sacramento
Sacramento, California
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- Call 714-988-2021
Ark Clinical Research - Fountain Valley
Fountain Valley, California
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- Call 714-474-2173
Southern California Clinical Research
Santa Ana, California
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- Call 310-265-1623
Peninsula Research Associates
Rolling Hills Estates, California
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- Call 203-437-6856
Chase Medical Research, LLC
Waterbury, Connecticut
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- Call 352-383-8222
Adult Medicine of Lake County, Inc.
Mt. Dora, Florida
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- Call 954-237-3799
American Research Centers of Florida
Pembroke Pines, Florida
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- Call 786-238-7110
BioMed Research & Medical Center
Miami, Florida
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- Call 561-968-2933
JEM Research Institute
Atlantis, Florida
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- Call 727-521-9137
IMA Clinical Research St. Petersburg
St. Petersburg, Florida
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- Call 850-476-3131 x53026
AHF Pensacola
Pensacola, Florida
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- Call 470-403-4755
Teak Research Consults - Dunwoody
Dunwoody, Georgia
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- Call 770-507-6867
Clinical Research Atlanta
Stockbridge, Georgia
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- Call 808-531-6886
East-West Medical Research Institute
Honolulu, Hawaii
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- Call 785-354-9591
Cotton O'Neil Clinical Research Center
Topeka, Kansas
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- Call 337-602-6642
Care Access - Lake Charles (Bayou Pines)
Lake Charles, Louisiana
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- Call 443-444-6275
MedStar Good Samaritan Hospital
Baltimore, Maryland
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- Call 443-444-5663
MedStar Health Research Institute (MedStar Physician Based Research Network)
Hyattsville, Maryland
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- Call 877-791-0656
Care Access - Quincy
Quincy, Massachusetts
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- Call 248-312-0025
Arcturus Healthcare , PLC, Troy Internal Medicine Research Division
Troy, Michigan
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- Call 702-597-9825
AMR Clinical
Las Vegas, Nevada
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- Call 505-224-7407
Albuquerque Clinical Trials, Inc.
Albuquerque, New Mexico
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- Call 585-288-0890
Rochester Clinical Research, LLC
Rochester, New York
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- Call 704-283-7359
Monroe Biomedical Research
Monroe, North Carolina
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- Call 724-912-0033
Preferred Primary Care Physicians
Uniontown, Pennsylvania
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- Call 843-849-1880
Accellacare - Mt Pleasant
Mt. Pleasant, South Carolina
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- Call 864-334-0141
Tribe Clinical Research, LLC
Greenville, South Carolina
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- Call 630-491-1900
AMR Clinical
Nashville, Tennessee
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- Call 713-486-1350
The University of Texas Health Science Center at Houston
Bellaire, Texas
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- Call 210-692-7157
IMA Clinical Research San Antonio
San Antonio, Texas
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- Call 757-627-7446
AMR Clinical
Norfolk, Virginia
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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.