Summary

Eligibility
for people ages 10-65 (full criteria)
Location
at UC Irvine UCLA UCSF
Dates
study started
completion around

Description

Summary

The purpose of this study is to evaluate the efficacy, safety, tolerability, and pharmacokinetics (PK) of VX-147 in adult and pediatric participants with apolipoprotein L1 (APOL1)-mediated proteinuric kidney disease.

Official Title

A Phase 2/3 Adaptive, Double-blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of VX-147 in Adult and Pediatric Subjects With APOL1-mediated Proteinuric Kidney Disease

Keywords

Proteinuric Kidney Disease, Kidney Diseases, VX-147

Eligibility

You can join if…

Open to people ages 10-65

You CAN'T join if...

Locations

  • UCLA Division of Nephrology accepting new patients
    Los Angeles California 90095 United States
  • UCI Center for Clinical Research accepting new patients
    Orange California 92868 United States
  • UCSF School of Medicine accepting new patients
    San Francisco California 94143 United States
  • Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center accepting new patients
    Torrance California 90502 United States
  • Cedars-Sinai Medical Center accepting new patients
    Los Angeles California 90048 United States
  • The Medical Research Group, Inc accepting new patients
    Fresno California 93720 United States
  • Kaiser Permanente - Los Angeles Medical Center accepting new patients
    Los Angeles California 90027 United States
  • Renal Consultants Medical Group accepting new patients
    Granada Hills California 91344 United States
  • Eastside Clinical Research Associates accepting new patients
    Los Angeles California 90022 United States
  • Kaiser Permanente, Sacramento accepting new patients
    Sacramento California 95825 United States

Details

Status
accepting new patients
Start Date
Completion Date
(estimated)
Sponsor
Vertex Pharmaceuticals Incorporated
ID
NCT05312879
Phase
Phase 2/3 Kidney Disease Research Study
Study Type
Interventional
Participants
Expecting 466 study participants
Last Updated