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Search / Trial NCT06859268

A Study of Retatrutide (LY3437943) in the Maintenance of Weight Reduction in Individuals With Obesity

Launched by ELI LILLY AND COMPANY · Feb 28, 2025

Trial Information

Current as of June 24, 2025

Recruiting

Keywords

ClinConnect Summary

This clinical trial is studying a medication called retatrutide, which is being tested to see how well it helps people with obesity maintain their weight loss. The study will last around 125 weeks and is divided into two parts. First, all participants will take a specific dose of retatrutide for 80 weeks. Then, in the next 36 weeks, participants will be randomly assigned to continue with their retatrutide dose, switch to a higher dose, or receive a placebo (a treatment that looks like the medication but has no active ingredients).

To join the study, participants need to be adults aged 18 and older who have obesity and have tried to lose weight through diet without success. However, some individuals won't be able to participate if they have recently lost or gained a significant amount of weight, have certain medical conditions (like diabetes or heart issues), or have undergone prior obesity treatments. Throughout the trial, participants will receive regular health check-ups and support while taking the medication. This study aims to gather important information about how retatrutide can help people keep their weight off in the long term.

Gender

ALL

Eligibility criteria

  • 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 Type 1 Diabetes, Type 2 Diabetes, or any other type of diabetes
  • 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)
  • 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
  • Have taken weight loss drugs, including over-the-counter medications, within 90 days prior to screening

About Eli Lilly And Company

Eli Lilly and Company is a global healthcare leader dedicated to creating innovative medicines that improve patient outcomes across a range of therapeutic areas, including diabetes, oncology, immunology, and neurodegenerative diseases. With a rich history of scientific research and a commitment to advancing healthcare, Lilly invests significantly in clinical trials to develop new treatments and enhance existing therapies. The company prioritizes patient safety and ethical standards in its clinical research, fostering collaboration with healthcare professionals and stakeholders to ensure the delivery of high-quality, evidence-based solutions that address unmet medical needs worldwide.

Locations

Boston, Massachusetts, United States

Duncansville, Pennsylvania, United States

West Palm Beach, Florida, United States

Baton Rouge, Louisiana, United States

Richmond, Virginia, United States

Louisville, Kentucky, United States

Woodstock, Georgia, United States

Blackpool, Lancashire, United Kingdom

Bellevue, Washington, United States

Aurora, Colorado, United States

Brampton, Ontario, Canada

Morehead City, North Carolina, United States

Cooper City, Florida, United States

Toronto, Ontario, Canada

Ocala, Florida, United States

Amherst, New York, United States

San Antonio, Texas, United States

Bradford On Avon, Wiltshire, United Kingdom

Hamden, Connecticut, United States

Poole, , United Kingdom

Mesquite, Texas, United States

Blackpool, , United Kingdom

Knoxville, Tennessee, United States

Trois Rivières, Quebec, Canada

Kansas City, Missouri, United States

Raleigh, North Carolina, United States

Lexington, Kentucky, United States

Terrebonne, Quebec, Canada

Blackburn, Lancashire, United Kingdom

Rapid City, South Dakota, United States

Burlington, Ontario, Canada

Wenatchee, Washington, United States

Coral Gables, Florida, United States

Moore, Oklahoma, United States

Oak Brook, Illinois, United States

Cheadle, Staffordshire, United Kingdom

Birmingham, , United Kingdom

Orlando, Florida, United States

Courtice, Ontario, Canada

Bromborough, Wirral, United Kingdom

Las Vegas, Nevada, United States

Santa Ana, California, United States

Lake Charles, Louisiana, United States

Thunder Bay, Ontario, Canada

Houston, Texas, United States

Honolulu, Hawaii, United States

Torpoint, Cornwall, United Kingdom

Hamilton, Ontario, Canada

Marietta, Georgia, United States

Springfield, Illinois, United States

Penzance, Cornwall, United Kingdom

Oxford, England, United Kingdom

Hounslow, London, United Kingdom

Rotherham, , United Kingdom

Hounslow, London, City Of, United Kingdom

Thunder Bay, Ontario, Canada

Patients applied

BH

LS

AS

4 patients applied

Trial Officials

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)

Study Director

Eli Lilly and Company

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported