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Search / Trial NCT07035093

A Study of Retatrutide (LY3437943) in Participants Who Have Obesity or Overweight and Chronic Low Back Pain

Launched by ELI LILLY AND COMPANY · Jun 16, 2025

Trial Information

Current as of June 26, 2025

Not yet recruiting

Keywords

Axial Predominant Low Back Pain

ClinConnect Summary

This clinical trial is studying a new medicine called retatrutide to see if it can help reduce long-lasting low back pain in people who are overweight or have obesity. The study will look at how well the medicine works and whether it is safe to use. Participants will be involved in the study for about 80 weeks, which is a little over a year and a half.

People who might be eligible to join are adults between 65 and 74 years old who have ongoing low back pain mainly in the lower back area, with or without pain spreading to the upper legs. They must have a body weight that classifies them as overweight or obese (a BMI of 27 or higher) and have tried at least once before to lose weight through diet without success. The study does not include people who have certain types of back pain, recent spine injections, significant recent weight changes, recent use of weight-loss drugs, prior or planned weight-loss surgery, or any form of diabetes. If you join, you can expect to be monitored closely over the study period to track your pain and any side effects from the medicine. This study is not yet open for enrollment but aims to find better treatments for people struggling with both weight issues and chronic low back pain.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Have a history of axial-predominant low back pain
  • Have pain that is restricted to the low back or with a referral pattern limited to the proximal legs
  • Have a body mass index (BMI) ≥27 kilograms per square meter (kg/m2) at screening
  • Have a history of at least 1 self-reported unsuccessful dietary effort to lose body weight
  • Exclusion Criteria:
  • Have a non-axial origin low back pain
  • Have had botulinum or steroid injections to the spine within 1 year of screening
  • Have had trigger point injection to the spine within 6 months of screening
  • Have a self-reported change in body weight \>5 kilograms (kg) (11 pounds) within 90 days prior to screening
  • Have been taking drugs to promote body weight reduction, including over-the-counter medications, within 90 days prior to screening
  • Have a prior or planned surgical treatment for obesity
  • Have Type 1 Diabetes, Type 2 Diabetes, or any other type of diabetes

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

Duncansville, Pennsylvania, United States

Winston Salem, North Carolina, United States

Bay City, Michigan, United States

Austin, Texas, United States

Topeka, Kansas, United States

Gdansk, Pomorskie, Poland

Miami, Florida, United States

Brampton, Ontario, Canada

Boulder, Colorado, United States

San Diego, California, United States

Guadalajara, Jalisco, Mexico

Toronto, Ontario, Canada

Danville, Virginia, United States

Fullerton, California, United States

Winter Park, Florida, United States

Krakow, , Poland

Sarnia, Ontario, Canada

Waltham, Massachusetts, United States

Knoxville, Tennessee, United States

Mérida, , Mexico

Ciudad Madero, Tamaulipas, Mexico

Dallas, Texas, United States

Lublin, Lubelskie, Poland

Białystok, Podlaskie, Poland

Rosario, Santa Fe, Argentina

Chandler, Arizona, United States

Granadero Baigorria, Santa Fe, Argentina

Santa Fe, , Argentina

Tampa, Florida, United States

Warszawa, Mazowieckie, Poland

Houston, Texas, United States

The Villages, Florida, United States

Poznań, Wielkopolskie, Poland

Springfield, Missouri, United States

Sydney, Nova Scotia, Canada

Veracruz, , Mexico

Lodz, , Poland

Lake Charles, Louisiana, United States

Ciudad Autónoma De Buenos Aires, Buenos Aires, Argentina

Buenos Aires, , Argentina

Fountain Valley, California, United States

Hamilton, Ontario, Canada

Saint Petersburg, Florida, United States

Mexico City, , Mexico

Buenos Aires, , Argentina

Ciudad Autonoma De Buenos Aires, , Argentina

Buenos Aires, , Argentina

Monterrey, , Mexico

Monterrey, , Mexico

Tucson, Arizona, United States

Daytona Beach, Florida, United States

Rosario, Santa Fe, Argentina

Patients applied

0 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