Related Experiment Video
Updated: Oct 23, 2025

Use of Ultra-high Field MRI in Small Rodent Models of Polycystic Kidney Disease for In Vivo Phenotyping and Drug Monitoring
Published on: June 23, 2015
TAMEing ADPKD with metformin: safe and effective?
Albert C M Ong1, Ron T Gansevoort2
1Kidney Genetics Group, Academic Nephrology Unit, Department of Infection, Immunity and Cardiovascular Disease, University of Sheffield Medical School, Beech Hill Road, Sheffield, UK.
Metformin, a diabetes drug, shows promise for slowing autosomal dominant polycystic kidney disease (ADPKD) progression. The TAME PKD trial found metformin safe and well-tolerated in early-stage ADPKD patients.
Area of Science:
- Nephrology
- Pharmacology
- Genetics
Background:
- Autosomal dominant polycystic kidney disease (ADPKD) is a common genetic disorder.
- Current treatments for ADPKD primarily manage symptoms and slow disease progression.
- Metformin, a widely used type 2 diabetes medication, has shown potential in preclinical models for ADPKD.
Purpose of the Study:
- To evaluate the safety and tolerability of metformin in patients with early-stage ADPKD.
- To assess the potential of metformin as a disease-modifying therapy for ADPKD.
Main Methods:
- The Trial of Administration of Metformin in PKD (TAME PKD) was a phase 2 randomized controlled trial.
- Participants were patients in the early stages of autosomal dominant polycystic kidney disease.
- The study investigated the safety and tolerability profiles of metformin.
Main Results:
- Metformin was found to be safe and well-tolerated in patients with early-stage ADPKD.
- The findings support further investigation into metformin's efficacy for ADPKD.
Conclusions:
- Metformin is a viable therapeutic option for further study in autosomal dominant polycystic kidney disease.
- These results inform the design and expectations for upcoming phase 3 trials in ADPKD.
More Related Videos
Related Concept Videos
Oral Hypoglycemic Agents: Biguanides and Glitazones
Chronic Kidney Disease I: Introduction
Chronic Kidney Disease III: Interprofessional Care
Drug Dosing in Renal Diseases: Estimation of Glomerular Filtration Rate Based on Serum Creatinine Concentration
Chronic Kidney Disease II: Clinical Manifestations
Pharmacokinetics in Obese Patients: Drug Absorption and Distribution

