A study testing whether a new weekly shot from Lilly, retatrutide, can help with weight.
- Who can join
- Adults 18+, have obesity who also have ongoing low back pain, BMI 27+.
- What you take
- retatrutide, given as part of the study at no cost to you. Some participants may receive a placebo (an inactive version) instead, decided at random.
- How long it lasts
- The full study runs about 2.3 years; your own time in it is usually shorter.
- What you get
- The study medication and study-related care at no cost. Compensation varies by study site; many cover travel and provide the study medication at no cost. The trial coordinator will explain what that site offers before you join.
What this study is for
Full study title: A Study of Retatrutide (LY3437943) in Participants Who Have Obesity or Overweight and Chronic Low Back Pain.
Primary condition: Obesity. Also studied in: Overweight, Chronic Low Back Pain (CLBP).
Who can join, in detail
Key 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
Key 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
Where this study is enrolling
This trial has 25 US sites across 14 states. Contact the site coordinator directly to start the screening process.
Arizona
- MD First Research - ChandlerChandler, Arizona480-508-1038
- Tucson Orthopaedic Institute - North Wyatt DriveTucson, Arizona520-404-0276
California
- Ark Clinical Research - Fountain ValleyFountain Valley, California714-988-2021
- St Joseph Heritage HealthcareFullerton, California714-626-8610
- Clinical Research InstituteLos Angeles, California323-879-9999
- Artemis Institute for Clinical ResearchSan Diego, California858-278-3647
Colorado
- Alpine Clinical Research CenterBoulder, Colorado303-443-7229
Florida
- K2 Medical Research - Daytona BeachDaytona Beach, Florida
- Flourish Research - Miami, LLCMiami, Florida305-631-6704
- IMA Clinical Research St. PetersburgSt. Petersburg, Florida727-521-9137
- Care Access - TampaTampa, Florida813-771-5980
- Charter Research - Lady LakeThe Villages, Florida
- Conquest ResearchWinter Park, Florida407-916-0060
Kansas
- Cotton O'Neil Clinical Research CenterTopeka, Kansas785-354-9591
Louisiana
- Care Access - Lake Charles (Bayou Pines)Lake Charles, Louisiana337-602-6642
Massachusetts
- MedVadis Research CorporationWaltham, Massachusetts617-744-1310
Michigan
- Great Lakes Research Group, Inc.Bay City, Michigan989-895-9100
Missouri
- Clinvest Headlands LlcSpringfield, Missouri417-883-7889
North Carolina
- Center for Clinical ResearchWinston-Salem, North Carolina
Pennsylvania
- Altoona Center For Clinical ResearchDuncansville, Pennsylvania814-693-0300
Tennessee
- New Phase Research and DevelopmentKnoxville, Tennessee
Texas
- FutureSearch Trials of NeurologyAustin, Texas512-380-9925
- Mercy Family ClinicDallas, Texas281-944-3610
- Houston Research InstituteHouston, Texas281-809-3234
Virginia
- Sovah Clinical Research-River DistrictDanville, Virginia
Timeline
Started enrolling: 2025-05-29. Expected completion: 2027-09. Last updated on ClinicalTrials.gov: 2026-05-20.
Official source
We sync this data quarterly from ClinicalTrials.gov, the federal registry for clinical research. Before contacting a site, verify the trial is still recruiting on the official page:
Other GLP-1 clinical trials
Back to the full directory → or take the matching quiz if you want clinical trials filtered to your conditions and location.