De observación
Los investigadores hacen un seguimiento de los resultados de salud a lo largo del tiempo en grupos de participantes para buscar patrones que nos ayuden a comprender mejor una enfermedad.
VX-NEN-801
A Study of the Prevalence of Apolipoprotein L1 (APOL1) Alleles Among Individuals With Proteinuric Kidney Disease Who Are of Recent African Ancestry or Geographic Origin
Breve descripción
A Study of the Prevalence of Apolipoprotein L1 (APOL1) Alleles Among Individuals With Proteinuric Kidney Disease Who Are of Recent African Ancestry or Geographic Origin.
Nombre del sitio
Renal Medicine Associates
3821 Masthead St NE Albuquerque, NM 87109
Nombre del patrocinador
Vertex Pharmaceuticals
Matrícula estimada
2500
Fecha estimada de finalización
30 June 2025
De observación
Los investigadores hacen un seguimiento de los resultados de salud a lo largo del tiempo en grupos de participantes para buscar patrones que nos ayuden a comprender mejor una enfermedad.
VX-NEN-801
A Study of the Prevalence of Apolipoprotein L1 (APOL1) Alleles Among Individuals With Proteinuric Kidney Disease Who Are of Recent African Ancestry or Geographic Origin
Breve descripción
A Study of the Prevalence of Apolipoprotein L1 (APOL1) Alleles Among Individuals With Proteinuric Kidney Disease Who Are of Recent African Ancestry or Geographic Origin.
El ensayo es para personas con
Chronic kidney disease not caused by diabetes, a history of proteinuria and no other identifiable cause of kidney disease
Objetivo del estudio
This clinical research study is investigating how many individuals with chronic kidney disease (CKD) not caused by diabetes have a genetic form of the disease due to a variation in the apolipoprotein L1 (APOL1) gene.
Qué implica para el paciente?
Patient will be asked to provide a blood and saliva sample on the day of visit. There will only be one (1) visit for this study. Study participants will be contacted and informed of the genetic test results when they become available.
