Stopped: Sponsor decision for administrative reasons
This is a study with 2 parts. Part 1 comprises a visit to collect biological samples necessary for the molecular characterization of chronic kidney disease. Part 2 comprises an observational period of 5 visits over a period up to 8 weeks. During Part 2, baseline tests will be conducted, and urine will be collected approximately every 2 weeks for 8 weeks. Patients may participate in Part 1, Part 2, or both, and will be followed for up to 1 year consisting of data collection from the patient's medical records and home collection of urine samples every 4 months.
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Change in Urine Protein-to-Creatinine Ratio (UPCR)
Timeframe: Approximately 1 year
Change in Urine Albumin-to-Creatinine Ratio (UACR)
Timeframe: Approximately 1 year
Estimated Glomerular Filtration Rate (eGFR)
Timeframe: Baseline/Biomarker collection visit
Change in Estimated Glomerular Filtration Rate (eGFR)
Timeframe: Approximately 8 weeks
Change in Urine Biomarker: Nephrin
Timeframe: Approximately 1 year
Change in Urine Biomarker: Podocin
Timeframe: Approximately 1 year
Change in Urine Biomarker: Rac1
Timeframe: Approximately 1 year
Change in Urine Biomarker: Synaptopodin
Timeframe: Approximately 1 year
Change in Urine Biomarker: Urea
Timeframe: Approximately 1 year
Change in Urine Biomarker: Other Exploratory
Timeframe: Approximately 1 year
Change in Serum/Plasma Biomarker: Other Exploratory
Timeframe: Approximately 8 weeks
Number of patients with genetic variants predicted to be associated with chronic kidney disease and functional consequence
Timeframe: Baseline/Biomarker collection visit
Gene expression profile and phenotype of inducible pluripotent stem cell (iPSC)-generated organoids
Timeframe: Baseline/Biomarker collection visit
Change from Baseline Patient-reported Assessment of FSGS Symptoms
Timeframe: Approximately 8 weeks
Change from Baseline Patient-reported Assessment of Health Status
Timeframe: Approximately 8 weeks
Change from Baseline Patient-reported Assessment of Fatigue
Timeframe: Approximately 8 weeks
Change from Baseline Clinician-reported Assessment of Edema
Timeframe: Approximately 8 weeks
Incidence of Untoward Medical Occurrences
Timeframe: Approximately 1 year
% of Patients with Change in Treatment
Timeframe: Approximately 1 year