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/AClinical Study ID
NCT04258397
H200014
U01DK111510
Ages > 21 All Genders
Study Summary
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
Connect with a study center
VA San Diego Healthcare System
San Diego, California 92161
United StatesActive - Recruiting
University of California, San Francisco
San Francisco, California 94143
United StatesActive - Recruiting

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