RecruitingPhase 4NCT06191848

Subcutaneous Tirzepatide Once-weekly in Patients With Obesity and Knee Osteoarthritis (STOP KNEE-OA)

Effect of Subcutaneous Tirzepatide Once-weekly in Patients With Obesity and Knee Osteoarthritis (STOP KNEE-OA): A Randomized, Double-Blind, Placebo-Controlled Trial

Sponsor

University of Melbourne

Enrollment

352 participants

Start Date

Nov 19, 2024

Study Type

INTERVENTIONAL

Conditions

Obesity Knee Osteoarthritis Osteoarthritis, Knee

Summary

This is a trial of tirzepatide in people with obesity and knee osteoarthritis. The main purpose of this study is to see if tirzepatide can reduce number of these participants who require a knee replacement. Participants will be randomized to take a weekly injection of tirzepatide or a placebo for a total of 72 weeks.

Eligibility

Min Age: 18 Years

Inclusion Criteria14

Have a body mass index of ≥ to 30 kg/m2.
Report one or more previous unsuccessful attempt to lose body weight via lifestyle modification.
Have been deemed eligible to enter the waiting list for primary knee replacement for the treatment of osteoarthritis in the target joint by an orthopaedic surgeon at one of the participating study sites.
Have moderate-to-severe knee osteoarthritis in the target joint, defined as a Kellgren-Lawrence grade two or greater.
Be willing to and capable of learning how to self-inject the study drug and follow study procedures for the duration of the trial.
Provide informed consent to study participation in line with the requirements of the human research ethics committee of the study site.
Female participants must:
Not be currently pregnant or breastfeeding AND
Not be of reproductive potential, defined as:
Infertile due to surgical sterilization or congenital anomaly, OR
Post-menopausal defined as:
A woman over the age of 40 years with spontaneous cessation of menses for at least 12 consecutive months (in the absence of medications known to induce amenorrhea), with a follicle-stimulating hormone ≥40mIU/mL, and a negative pregnancy test prior to study entry, OR
A woman over the age of 55 years with cessation of menses for at least 12 consecutive months (in the absence of medications known to induce amenorrhea), OR
A woman over the age of 55 years that has commenced hormone replacement therapy after a documented diagnosis of menopause.

Exclusion Criteria27

Participant will be ineligible for inclusion if they meet any of the following criteria:
Have been deemed eligible to enter the waiting list for knee replacement in the contralateral knee by an orthopaedic surgeon at one of the participating study sites.
Have used any prescription medications intended to promote weight loss (e.g., tirzepatide, liraglutide, semaglutide) in the three months prior to screening.
Have previously undergone any surgical or endoscopic procedure intended to promote weight loss.
Have been diagnosed with type 1 diabetes mellitus (T1DM) or T2DM
Have laboratory evidence indicative of diabetes mellitus during screening.
Have personal or family history of medullary thyroid carcinoma (MTC) or Multiple Endocrine Neoplasia syndrome type 2 (MEN 2)
Have an active malignancy (excluding basal or squamous cell skin cancer).
Have had a transplanted organ or awaiting an organ transplant
Have received chronic systemic glucocorticoid therapy (for more than 14 days) in prior 3 months or have a significant, active autoimmune abnormality (e.g., lupus or rheumatoid arthritis) that the study doctor deems likely to require systemic glucocorticoid therapy during the next 18 months.
Have any other medical conditions, abnormal laboratory tests or concomitant medications that make them unsuitable for participation:
Have a clinically significant gastric emptying abnormality.
Have had a history of acute or chronic pancreatitis.
Have obesity induced by other endocrinologic disorders
Have an unstable psychiatric disorder
Have a Patient Health Questionnaire (PHQ-9) score of >15 during screening
Have been deemed by the study doctor to be actively suicidal,
Have answered "yes" to questions 4 or 5 on the "Suicidal Ideation" section of the Columbia-Suicide Severity Rating Scale (C-SSRS) during screening, OR
Have answered yes to any questions in the "Suicidal Behaviour" section of the C-SSRS during screening. AND
The behaviour or ideation occurred in the last month
Have uncontrolled hypertension (systolic blood pressure above or equal to 160 mmHg and/or diastolic blood pressure above or equal to 100 mmHg)
Have severe renal impairment defined as an eGFR <30 mL/min/1.73 m2 at screening visit.
Have thyroid-stimulating hormone outside of the range of 0.4 to 6.0 mIU/L at screening visit
Have acute or chronic hepatitis or abnormal liver function tests as measured by either alanine aminotransferase or alkaline phosphatase >200 IU.
Have any other known contraindication to any glucagon-like peptide-1 receptor agonists.
Are study site personnel, or immediate family of a member of the study site.
Have been enrolled in any other study of an investigational product within the past ninety days or are currently enrolled in such a study.