Human Urine Sample Collection for Alport Nephropathy Biomarker Studies

Novartis Pharmaceuticals80 enrolled

Overview

This is a prospective cross-sectional, observational, single-center study of Alport patients, in which a single, first morning voided urine collection will be acquired and used to validate assays of urine biomarkers that reflect changes in glomerular protein filtration barrier function. The purpose of this study is to identify biomarkers indicative of changes in glomerular filtration function that occur during the course of proteinuric renal diseases such as Alport nephropathy.

Study Type

OBSERVATIONAL

Enrollment

Conditions

Alport Syndrome

Eligibility

Sex: ALLMin age: 5 Years

Medical Language ↔ Plain English

Inclusion criteria: * Alport syndrome diagnosis (clinical and/or histopathologic and/or genetic diagnosis, per subject's physician and/or genotyping) * Physically able to provide a single first-morning urine sample of at least 30 mL Exclusion criteria: * Diagnosis of chronic kidney disease * Receiving chronic phosphate-lowering therapy or erythropoietin therapy * Ongoing chronic hemodialysis therapy and/or renal transplant recipient * Nephrotic-range proteinuria: spot urine protein-to-creatinine ratio ≥ 3 on at least 2 of the last 3 clinical assessments Other protocol-defined inclusion/exclusion criteria may apply

Data from ClinicalTrials.gov

This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.