Glucagon-Like Peptide-1 Receptor Agonist in ADPKD

Recruiting now · Phase 2 · Has a placebo group

Conditions studied: Autosomal Dominant Polycystic Kidney, Obesity

In brief

The proposed clinical trial aims to assess if a year of treatment with a glucagon-like peptide 1 receptor agonist, a medication approved for weight management that also improves the body's response to glucose and insulin, can slow kidney growth in adults with autosomal dominant polycystic kidney disease who are overweight or obese. The study will also evaluate changes in abdominal fat and kidney metabolism using cutting-edge images techniques. Blood and urine samples will provide further insight into biological changes that may be linked to the benefits of the intervention, while ensuring careful monitoring of safety and tolerability.

Key facts

Study ID

NCT06582875

Run by

University of Colorado, Denver

People needed

126

Starts

2025-03-06

Expected to finish

2029-06-30

Last updated by the study team

2025-05-06

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 18-65 years of age
• ADPKD diagnosis based on the modified Pei-Ravine criteria
• Body-mass index of ≥27 kg/m\^2
• Estimated glomerular filtration rate ≥ 30 mL/min/1.73m\^2
• Mayo Classification of C, D, or E, calculated from a previous kidney ultrasound or MRI performed within the last 12 months
• Not currently participating in or planning to participate in any formal weight loss or physical activity program, or another interventional study
• Ability to provide informed consent

You may not qualify if…

• Diabetes mellitus
• Tolvaptan usage or plans to initiate tolvaptan
• History of hospitalization or major surgery within the last 3 months
• Uncontrolled hypertension (systolic blood pressure > 160 or diastolic blood pressure >100 mm Hg)
• Pregnancy, lactation, or unwillingness to use adequate birth control
• Regular use of prescription or over-the-counter medications that may affect weight, appetite, food intake, or energy metabolism
• History of clinically diagnosed eating disorder including: anorexia nervosa, bulimia, binge eating disorder
• Weight change of >5% in the past 3 months for any reason except post-partum weight loss
• Inability to cooperate with or clinical contraindication for MRI including: severe claustrophobia, implants, devices, or non-removable body piercings
• Presence or personal history of malignant neoplasm within 5 years prior to the day of screening
• Personal or family history of medullary thyroid carcinoma, thyroid nodule, or multiple endocrine neoplasia type 2
• Prior history of pancreatitis
• Weight ≥450 lb

Where it is running

• University of Colorado - Anschutz Medical Campus — Aurora, Colorado, United States (enrolling)

Full record on ClinicalTrials.gov

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