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Completed Phase 3 Interventional Accepts healthy volunteers Results available

Research Study Looking at How Well Semaglutide Works in People Suffering From Obesity and Knee Osteoarthritis

ClinicalTrials.gov ID: NCT05064735

Public ClinicalTrials.gov record NCT05064735. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 29, 2026, 7:37 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Effect of Subcutaneous Semaglutide 2.4 mg Once-weekly Compared to Placebo in Subjects With Obesity and Knee Osteoarthritis

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This study will look at participants body weight from the start to the end of the study. It will also look at how much pain participants have in participants knee from the start to the end of the study and how this affects participants daily life. This is to compare the effect on body weight and pain in the knee in people taking semaglutide with people taking "dummy" medicine. Participants will either get semaglutide or "dummy" medicine. Which treatment participants get is decided by chance. Participants will need to take 1 injection once a week. The study medicine is injected with a thin needle in a skin fold in the stomach, thigh or upper arm. During the study, participants will have talks with study staff about how to eat healthy food and how to be more physically active. The study will last for about 1 ½ years. Participants will have 14 clinic visits with the study staff. At the first clinic visit participants will have a blood sample taken. Participants will have an X-ray of participants knee taken at the first visit. If participants have had an X-ray recently, this may not be needed. At 6 of the clinic visits participants cannot take pain medications for 3 days before the visit. Participants cannot take part if participants have had a joint replacement surgery in participants knee. Participants cannot take part if participants have or have had diabetes. Women: Women cannot take part if pregnant, breast-feeding or plan to become pregnant during the study period.

Study identification

NCT ID
NCT05064735
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novo Nordisk A/S
Industry
Enrollment
407 participants

Conditions and interventions

Eligibility (public fields only)

Age range
Not listed
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 1, 2021 (Actual)
Primary completion
Jul 24, 2023 (Actual)
Completion
Sep 8, 2023 (Actual)
Last update posted
Nov 17, 2025

2021 – 2023

United States locations

U.S. sites
61
U.S. states
23
U.S. cities
55
Facility City State ZIP Site status
Baptist Health System Montgomery Alabama 36106 —
Ortho Arizona Phoenix Arizona 85018 —
Anaheim Clinical Trials, LLC Anaheim California 92801 —
Stuart L. Silverman MD - A Medical Corporation Beverly Hills California 90211 —
Valley Research Fresno California 93720 —
Providence Medical Foundation Fullerton California 92835 —
Desert Oasis Hlthcr Med Group Palm Springs California 92262 —
Encompass Clinical Research_Spring Valley Spring Valley California 91978 —
Diablo Clinical Research, Inc. Walnut Creek California 94598 —
Clinical Research of Hollywood_Hollywood Hollywood Florida 33024 —
Westside Center For Clinical Research Jacksonville Florida 32205 —
Jacksonville Ctr For Clin Res Jacksonville Florida 32216 —
Well Pharma Medical Research Corp Miami Florida 33143 —
Renstar Medical Research Ocala Florida 34470 —
Clinical Trial Res Assoc,Inc Plantation Florida 33324 —
East West Medical Research Institute_Honolulu Honolulu Hawaii 96814 —
Clinical Invest Special_Gurnee Gurnee Illinois 60031 —
Evanston Premier Hlthcr Res Skokie Illinois 60077 —
Clinical Invest Special_Gurnee Wauconda Illinois 60084 —
MediSphere Medical RC Evansville Indiana 47714 —
Velocity Clin. Res Valparaiso Valparaiso Indiana 46383 —
KU MedWest Shawnee Mission Kansas 66217 —
L-MARC Research Center Louisville Kentucky 40213 —
Maryland Veterans Administration Health Care System Baltimore Maryland 21201 —
Centennial Medical Group Elkridge Maryland 21075-6437 —
Brigham & Women's Hospital Boston Massachusetts 02115-5804 —
Arcturus Healthcare, PLC. Troy Michigan 48098 —
StudyMetrix Research LLC City of Saint Peters Missouri 63303 —
The Center For Pharmaceutical Research PC Kansas City Missouri 64114 —
Sundance Clinical Research LLC St Louis Missouri 63141 —
NYU Langone Medical Cent-Joan H Tisch Cnt for Women's Health New York New York 10010 —
Hospital For Special Surgery New York New York 10021 —
Rochester Clinical Research, Inc. Rochester New York 14609 —
DaVita Clinical Research - New York The Bronx New York 10461 —
Southgate Medical Group, LLP West Seneca New York 14224 —
Great Lakes Medical Research Westfield New York 14787 —
University of North Carolina- Chapel Hill Adults Chapel Hill North Carolina 27517 —
Medication Mgmnt, LLC_Grnsboro Greensboro North Carolina 27405 —
PharmQuest Life Sciences LLC Greensboro North Carolina 27408 —
Raleigh Medical Group Raleigh North Carolina 27609-7216 —
Accellacare Wilmington North Carolina 28401 —
Piedmont Medical Research Associates Winston-Salem North Carolina 27103 —
Velocity Clin Res_Cincinnati Cincinnati Ohio 45242 —
Louis Stokes Clvlnd VA Med Ctr Cleveland Ohio 44106-1702 —
Cleveland Clinic_Cleveland Cleveland Ohio 44195 —
Prestige Clinical Research Franklin Ohio 45005 —
New Venture Medical Research Wadsworth Ohio 44281 —
Altoona Osteoporosis Center Duncansville Pennsylvania 16635-8406 —
The University of Penn Center Philadelphia Pennsylvania 19104-3317 —
Parkside Family Medicine Philadelphia Pennsylvania 19144 —
Rhode Island Hospital Providence Rhode Island 02903 —
Accellacare US Inc._SC Mt. Pleasant South Carolina 29464 —
Coastal Carolina Res Ctr. North Charleston South Carolina 29405 —
Palmetto Clinical Research Summerville South Carolina 29485 —
Tennova HC Turkey Creek MC Knoxville Tennessee 37934 —
PrimeCare Medical Group Houston Texas 77024 —
Southwest Houston Research Ltd Houston Texas 77099 —
DM Clin Rsrch/Fam Diag Clinic Tomball Texas 77375 —
Health Res of Hampton Roads Newport News Virginia 23606 —
National Clin Res Inc. Richmond Virginia 23294 —
Capital Clin Res Ctr,LLC Olympia Washington 98502 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 61 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05064735, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Nov 17, 2025 · Synced Oct 29, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05064735 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →