Trial of Pirfenidone to Prevent Progression in Chronic Kidney Disease

Last updated: April 25, 2022
Sponsor: Veterans Medical Research Foundation
Overall Status: Active - Recruiting

Phase

2

Condition

Kidney Disease

Focal Segmental Glomerulosclerosis

Nephropathy

Treatment

N/A

Clinical Study ID

NCT04258397
H200014
U01DK111510
  • Ages > 21
  • All Genders

Study Summary

Kidney disease is a global health problem, affecting more than 10% of the world's population and more than half of adults over 70 years of age in the United States. Persons with kidney disease are at higher risk for cardiovascular disease, heart failure, physical function decline, and mortality. Kidney scarring is a dominant factor in the development of kidney disease. Our group has evaluated several tests to determine the severity of scarring without requiring kidney biopsies, using MRI imaging scans and evaluating markers of scarring that we can measure in the urine. In this study we will use these measures to evaluate pirfenidone as a promising potential new treatment for patients with kidney disease.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Patients with eGFR ≥20 ml/min/1.73m2 using the CKD-EPI Creatinine equation.
  • Four variable Kidney Failure Risk Equation (KFRE) 5 year risk score >1%
  • Age 21 years or older.

Exclusion

Exclusion Criteria: To be determined at the screening visit or, for laboratory data, within 3 months of thescreening visit if available from clinical care.

  • Participants with known autosomal dominant polycystic kidney disease.
  • Use or planned use of drugs that inhibit CYP1A2 which may increase pirfenidoneexposure ( for example, artemisin, atazanavir, cimetidine, ciprofloxacin, enoxacin,ethinyl estradiol, fluvoxamine, mexiletine, tacrine, thiabendazole, or zileuton).
  • Liver disease: clinical cirrhosis by imaging or physician diagnosis; alcohol use > 14drinks/week; or aspartate aminotransferase (AST), alanine aminotransferase (ALT), ortotal bilirubin concentrations > 2 times the upper limit of normal (ULN) based onthresholds set at each site's local clinical laboratory.
  • Clinical idiopathic pulmonary fibrosis (IPF) by imaging or physician diagnosis (pirfenidone is indicated for patients with IPF).
  • Electrocardiogram (ECG) with a QTc interval > 500 msec at screening (pirfenidone canprolong QTc).
  • Family or personal history of long QT Syndrome.
  • Known hypersensitivity to pirfenidone.
  • Current use of tobacco, including cigarettes, cigars, chewing tobacco, or vapingproducts. (Current use is defined as any use in the past 3 months).
  • Physical inability, claustrophobia or other contra-indication to obtaining MRImeasurements.
  • Current participation in another clinical trial (observational studies are exempted).
  • Systemic immunosuppressive medications (<10 mg daily prednisone or inhaled steroidsare exempted).
  • Malignancy within 2 years (non-melanoma skin and localized prostate carcinoma areexempted).
  • Institutionalized individuals (e.g. prisoners, long term care residents).
  • Pregnancy, planning to become pregnant, or currently breast-feeding; women under 55will need to either have a reliable method of birth control (IUD {intrauterinedevice}, oral contraceptive pills {OCPs}) or have no menses in the preceding 2 years.
  • Life expectancy < 12 months as assessed by the site investigator.
  • Plans to leave the immediate area in < 12 months.
  • Anticipated need for dialysis or kidney transplantation within 12 months.
  • Hospitalization within the past 30 days (24-hour observation admissions are exempted).
  • Active alcohol or substance abuse within the last 12 months, as assessed by the siteinvestigator.
  • Active treatment of uncontrolled psychiatric disease, as assessed by the siteinvestigator.
  • Perceived inability to adhere to the medical regimen or comply with recommendations,as determined by the site investigator.
  • Inability or unwillingness to travel to study visits.
  • Any condition that, in the opinion of the site investigator, might be significantlyexacerbated by the known side effects associated with the administration ofpirfenidone.

Study Design

Total Participants: 200
Study Start date:
October 26, 2020
Estimated Completion Date:
December 31, 2024

Study Description

The TOP-CKD clinical trial is a randomized, double-blind, placebo-controlled interventional study, phase 2 trial of pirfenidone vs. placebo in 200 persons with Chronic Kidney Disease (CKD) with an eGFR ≥ 20 ml/min/1.73 m2 and a risk of progression to End Stage Renal Disease (ESRD) of at least 1% over five years. Participants receive treatment for 12 months, followed by a 6 month off-treatment follow-up period. Kidney scarring, also known as fibrosis, is a dominant factor in the development of kidney disease. This study will evaluate several tests to determine the severity of scarring without requiring kidney biopsies, using MRI imaging scans and evaluating markers of scarring that we can measure in the urine. We will use these measures to evaluate pirfenidone as a promising potential new treatment for patients with CKD.

Connect with a study center

  • VA San Diego Healthcare System

    San Diego, California 92161
    United States

    Active - Recruiting

  • University of California, San Francisco

    San Francisco, California 94143
    United States

    Active - Recruiting

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