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NCT05931367CompletedPhase 3

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

A Phase 3 Study to Investigate the Efficacy and Safety of LY3437943 Once Weekly in Participants Who Have Obesity or Overweight and Osteoarthritis of the Knee: A Randomized, Double-Blind, Placebo-Controlled Trial

Source: ClinicalTrials.gov · Last updated 21 Jan 2026

Brief summary (registry, in English)

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.

Status (registry)
Completed
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
445 (actual)
First submitted
27 Jun 2023
Start date
1 Aug 2023
Primary completion date
14 Nov 2025
Lead sponsor
Eli Lilly and Company
Diseases
Obesity
NCT number
NCT05931367
EU CT number
2023-503660-17-00

What you commit to

  • Study type: Interventional · Phase 3
  • Participants enrolled: 445
  • From 1 Aug 2023 to the primary completion date, 14 Nov 2025
  • 48 sites in 6 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Have had steroid joint injections within 90 days of screening.
  • 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.

Other illness

  • Have joint disease other than osteoarthritis.
  • Have diabetes mellitus.

Other

  • Have had other joint injections and procedures within 6 months of screening.

Who the study is looking for

  • 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.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (48)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Paratus Clinical Research Western Sydney
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BlacktownAustraliaUnknown status
Emeritus Research
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BotanyAustraliaUnknown status
Core Research Group
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BrisbaneAustraliaUnknown status
Royal Brisbane and Women's Hospital
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BrisbaneAustraliaUnknown status
Paratus Clinical Research Canberra
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BruceAustraliaUnknown status
Emeritus Research
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CamberwellAustraliaUnknown status
Barwon Health
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GeelongAustraliaUnknown status
CDH Research Institute
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MaroochydoreAustraliaUnknown status
Viable Clinical Research
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BridgewaterCanadaUnknown status
C-health Research
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CalgaryCanadaUnknown status
Wharton Medical Clinic
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HamiltonCanadaUnknown status
Alpha Recherche Clinique
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QuébecCanadaUnknown status
Bluewater Clinical Research Group Inc.
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SarniaCanadaUnknown status
Viable Clinical Research
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Scarborough VillageCanadaUnknown status
Eastern Health - General Hospital
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St. John'sCanadaUnknown status
Stouffville Medical Research Institute Inc.
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StouffvilleCanadaUnknown status
Canadian Phase Onward
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TorontoCanadaUnknown status
Complexo Hospitalario Universitario A Coruña
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A CoruñaSpainCompleted
Hospital de la Santa Creu i Sant Pau
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BarcelonaSpainCompleted
Hospital Universitario Reina Sofia
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CórdobaSpainCompleted
Area Sanitaria De Ferrol
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FerrolSpainCompleted
Hospital Quironsalud Malaga
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MálagaSpainCompleted
Hospital Universitario Infanta Sofia
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San Sebastián de los ReyesSpainCompleted
Nuevas Tecnologias En Diabetes Y En Endocrinologia S.L. Profesional
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SevillaSpainCompleted
Hospital General Universitario de Valencia
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ValenciaSpainCompleted
Panthera Biopartners - North London
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EnfieldUnited KingdomUnknown status
Leicester General Hospital
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LeicesterUnited KingdomUnknown status
Panthera Biopartners - Sheffield
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SheffieldUnited KingdomUnknown status
Investigacion y Biomedicina de Chihuahua
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Chihuahua CityMexicoUnknown status
Centro de Estudios de Investigacion Metabolicos y Cardiovasculares
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Ciudad MaderoMexicoUnknown status
Consultorio Médico
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GuadalajaraMexicoUnknown status
Kohler and Milstein Research S.A. de C.V.
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MéridaMexicoUnknown status
Clínica García Flores SC
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MonterreyMexicoUnknown status
IMED Internal Medicine Clin Trials
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MonterreyMexicoUnknown status
Unidad Médica para la Salud Integral
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San Nicolás de los GarzaMexicoUnknown status
Great Lakes Research Group, Inc.
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Bay CityUnited StatesUnknown status
Northwest Clinical Research Center
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BellevueUnited StatesUnknown status
Elite Clinical Trials
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BlackfootUnited StatesUnknown status
Northwestern University
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ChicagoUnited StatesUnknown status
Mercy Family Clinic
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DallasUnited StatesUnknown status
Suncoast Research Group
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MiamiUnited StatesUnknown status
Arizona Research Center
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PhoenixUnited StatesUnknown status
Clinical Trials of Texas Inc
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San AntonioUnited StatesUnknown status
Artemis Institute for Clinical Research
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San DiegoUnited StatesUnknown status
Clinvest Research, LLC
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SpringfieldUnited StatesUnknown status
MedVadis Research Corporation
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WalthamUnited StatesUnknown status
Chase Medical Research, LLC
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WaterburyUnited StatesUnknown status
North Georgia Clinical Research
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WoodstockUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.