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A Study of Retatrutide (LY3437943) Once Weekly in Participants Who Have Obesity or Overweight and Osteoarthritis of the Knee

Obesity | Overweight | Osteo Arthritis Knee

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.

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Conditions de participation

  • Sexe:

    ALL
  • Âges admissibles:

    18 and up

Critères de participation

Inclusion Criteria:

* 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.

Exclusion Criteria:

* 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.

Lieu de l'étude

Wharton Medical Clinic
Wharton Medical Clinic
Hamilton, Ontario
Canada

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Canadian Phase Onward
Canadian Phase Onward
Toronto, Ontario
Canada

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Viable Clinical Research
Viable Clinical Research
Bridgewater, Nova Scotia
Canada

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Stouffville Medical Research Institute Inc.
Stouffville Medical Research Institute Inc.
Stouffville, Ontario
Canada

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C-health Research
C-health Research
Calgary, Alberta
Canada

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Bluewater Clinical Research Group Inc.
Bluewater Clinical Research Group Inc.
Sarnia, Ontario
Canada

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Eastern Health - General Hospital
Eastern Health - General Hospital
St. John's, Newfoundland and Labrador
Canada

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Viable Clinical Research
Viable Clinical Research
Scarborough, Ontario
Canada

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Étude parrainée par
Eli Lilly and Company
Participants recherchés
Plus d'informations
ID de l'étude: NCT05931367