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.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
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
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