A Study of Retatrutide (LY3437943) Once Weekly in Participants Who Have Obesity or Overweight and Osteoarthritis of the Knee
Completed · Phase 3 · Has a placebo group
Conditions studied: Obesity, Overweight, Osteo Arthritis Knee
In brief
The main purpose of this study is to evaluate the safety and efficacy of retatrutide once-weekly in participants who have obesity or are overweight and have osteoarthritis (OA) of the knee. The study will lasts about 77 weeks.
Key facts
- Study ID
- NCT05931367
- Run by
- Eli Lilly and Company
- People needed
- 445
- Starts
- 2023-08-01
- Expected to finish
- 2025-11-14
- Last updated by the study team
- 2026-01-21
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Have a body mass index (BMI) ≥27 kilogram/kg/m² at screening.
- Have a history of at least 1 self-reported unsuccessful dietary effort to lose body weight.
- Have index knee pain for >12 weeks prior to screening, and presence of index knee pain for >15 days over the previous month.
- Have knee X-ray with moderate radiographic changes (Kellgren-Lawrence Grade 2 or 3) per central reading at screening.
- Currently meets American College of Rheumatology (ACR) Criteria (clinical and radiological) for OA.
You may not qualify if…
- Have had steroid joint injections within 90 days of screening.
- Have had other joint injections and procedures within 6 months of screening.
- Have joint disease other than osteoarthritis.
- Have a self-reported or documented change in body weight >5 kg (11 pounds) within 90 days prior to screening.
- Have been taking weight loss drugs, including over-the-counter medications, within 90 days prior to screening.
- Have a prior or planned surgical treatment for obesity.
- Have diabetes mellitus.
Where it is running
- Arizona Research Center — Phoenix, Arizona, United States
- Artemis Institute for Clinical Research — San Diego, California, United States
- Chase Medical Research, LLC — Waterbury, Connecticut, United States
- Suncoast Research Group — Miami, Florida, United States
- North Georgia Clinical Research — Woodstock, Georgia, United States
- Elite Clinical Trials — Blackfoot, Idaho, United States
- Northwestern University — Chicago, Illinois, United States
- MedVadis Research Corporation — Waltham, Massachusetts, United States
- Great Lakes Research Group, Inc. — Bay City, Michigan, United States
- Clinvest Research LLC — Springfield, Missouri, United States
- Mercy Family Clinic — Dallas, Texas, United States
- Clinical Trials of Texas, Inc. — San Antonio, Texas, United States
- Northwest Clinical Research Center — Bellevue, Washington, United States
- Paratus Clinical Research Canberra — Bruce, Australian Capital Territory, Australia
- Paratus Clinical Research Western Sydney — Blacktown, New South Wales, Australia
- Emeritus Research — Botany, New South Wales, Australia
- Royal Brisbane and Women's Hospital — Brisbane, Queensland, Australia
- Core Research Group — Brisbane, Queensland, Australia
- CDH Research Institute — Maroochydore, Queensland, Australia
- Emeritus Research — Camberwell, Victoria, Australia
- Barwon Health — Geelong, Victoria, Australia
- C-health Research — Calgary, Alberta, Canada
- Eastern Health - General Hospital — St. John's, Newfoundland and Labrador, Canada
- Viable Clinical Research — Bridgewater, Nova Scotia, Canada
- Wharton Medical Clinic — Hamilton, Ontario, Canada
Full record on ClinicalTrials.gov
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