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HomeTrials › NCT06662383

Obesity & weight · Phase 3 · Active, not recruiting

A Study of Retatrutide (LY3437943) Compared to Tirzepatide (LY3298176) in Adults Who Have Obesity

NCT06662383 · Sponsor: Eli Lilly and Company

What this trial means for you

This study is active, not recruiting — it is not currently taking new participants, but its results may matter for treatments you're considering. It's studying Retatrutide, Tirzepatide for obesity.

Who can joinAll sexes, 18 Years and older
Healthy volunteersNo — diagnosis required
What you'd takeRetatrutide, Tirzepatide
Study length~2.1 years overall
Planned participants800
TypeInterventional (you receive treatment)

What participants typically get: study medication (or placebo, if the trial uses one) and study-related medical care at no cost, plus close monitoring. Compensation for time and travel varies by study — ask the site. Note that in many trials you can't choose your treatment group, and some participants receive a placebo.

The study, in the sponsor's words

The main purpose of this study is to evaluate the efficacy and safety of retatrutide compared to tirzepatide in adults who have obesity. The study will last about 89 weeks.

Can you join? The exact criteria

Below is the verbatim eligibility text from the registry — bring it to your doctor; it's written for clinicians, and your own clinician is the right person to interpret it with you.

Full eligibility criteria (for you and your doctor)

Inclusion Criteria: * Have obesity and a history of at least one self-reported unsuccessful dietary effort to reduce body weight. Exclusion Criteria: * Have a self-reported change in body weight \>5 kilograms (kg) (11 pounds) within 90 days before screening. * Have a prior or planned surgical treatment for obesity. * Have a prior or planned endoscopic procedure and/or device-based therapy for obesity. * Have taken weight loss drugs, including over-the-counter medications, within 90 days prior to screening. * Have a family or personal history of medullary thyroid carcinoma (MTC) or multiple endocrine neoplasia syndrome type 2 (MEN-2). * Have had within the past 90 days before screening: * acute myocardial infarction * cerebrovascular accident (stroke) * coronary revascularization * hospitalization for unstable angina, or * hospitalization due to congestive heart failure. * Have New York Heart Association Functional Classification Class IV congestive heart failure. * Have a history of chronic or acute pancreatitis.

Study sites by state

Arizona

  • Medical Advancement Centers of Arizona — Tempe

California

  • Mary & Dick Allen Diabetes Center — Newport Beach
  • Artemis Institute for Clinical Research — San Diego
  • Encompass Clinical Research — Spring Valley
  • Diablo Clinical Research, Inc. — Walnut Creek

Colorado

  • Lynn Institute of Denver — Aurora

Connecticut

  • Bridgeport Hospital — Bridgeport
  • Yale University School of Medicine — New Haven

Florida

  • Encore Medical Research — Hollywood
  • Suncoast Research Group — Miami
  • Onhealth Research Center — Miami
  • Precision Clinical Research — Sunrise
  • Einstein Clinical Research — Vero Beach

Georgia

  • ClinCept Clinical Research - MH — Columbus
  • Northeast Georgia Medical Center — Gainesville
  • Pivotal Research Solutions — Stonecrest

Hawaii

  • East-West Medical Research Institute — Honolulu

Illinois

  • Northwestern University — Chicago

Iowa

  • Integrated Clinical Trial Services, Inc. — West Des Moines

Louisiana

  • Pennington Biomedical Research Center — Baton Rouge

Michigan

  • Great Lakes Research Group, Inc. — Bay City
  • Great Lakes Research Institute — Southfield

Missouri

  • StudyMetrix Research — City of Saint Peters

Nevada

  • Las Vegas Endocrinology — Henderson

New York

  • Albany Medical College, Division of Community Endocrinology — Albany
  • New York Gastroenterology Associates — New York
  • Westchester Medical Center — Valhalla

North Carolina

  • PharmQuest Life Sciences, LLC — Greensboro
  • Monroe Biomedical Research — Monroe
  • Accellacare - Wilmington — Wilmington

North Dakota

  • Lillestol Research — Fargo

Ohio

  • PriMED Clinical Research — Dayton

South Carolina

  • Tribe Clinical Research, LLC — Greenville

Tennessee

  • WR-Clinsearch, LLC — Chattanooga

Texas

  • Headlands Horizons LLC — Brownsville
  • Next Level Urgent Care — Houston
  • Houston Research Institute — Houston
  • Consano Clinical Research, LLC — Shavano Park

Utah

  • Chrysalis Clinical Research — St. George

Virginia

  • Charlottesville Medical Research — Charlottesville

View the official record on ClinicalTrials.gov →

Verify before you act. Medical disclaimer: content on this site is for informational purposes only and is not medical advice. GLP-1 medications are prescription drugs; always consult a licensed healthcare provider about eligibility, risks, and benefits. Trial details and enrollment status change frequently — always verify on the official registry and talk to your own clinician before contacting a study site. This page was generated from registry data and is not affiliated with the study sponsor.

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