A Phase 3, Randomized, Double-Blind, Placebo-Controlled Study to Investigate the Efficacy and Safety of Retatrutide Once Weekly in Participants Who Have Obesity or Overweight and Chronic Low Back Pain
Eli Lilly and Company
Summary
The main purpose of this study is to evaluate the efficacy and safety of retatrutide in relieving chronic low back pain in participants who have obesity or overweight. Participation in the study will last about 80 weeks.
Eligibility
- Age range
- 18+ years
- Sex
- All
- Healthy volunteers
- No
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 cha…
Interventions
- DrugRetatrutide
Administered SC
- DrugPlacebo
Administered SC
Locations (41)
- MD First Research - ChandlerChandler, Arizona
- Tucson Orthopaedic Institute - North Wyatt DriveTucson, Arizona
- Ark Clinical Research - Fountain ValleyFountain Valley, California
- St Joseph Heritage HealthcareFullerton, California
- Clinical Research InstituteLos Angeles, California
- Artemis Institute for Clinical ResearchSan Diego, California