← Back to Clinical Trials
Recruiting Phase 2, Phase 3 NCT05312879

Phase 2/3 Adaptive Study of VX-147 in Adult and Pediatric Participants With APOL1-Mediated Proteinuric Kidney Disease

Trial Parameters

Condition Proteinuric Kidney Disease
Sponsor Vertex Pharmaceuticals Incorporated
Study Type INTERVENTIONAL
Phase Phase 2, Phase 3
Enrollment 466
Sex ALL
Min Age 10 Years
Max Age 65 Years
Start Date 2022-03-30
Completion 2028-06-02
Interventions
VX-147Placebo

Brief 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.

Eligibility Criteria

Key Inclusion Criteria: Part A: * APOL1 genotype of G1/G1, G2/G2, or G1/G2 * Proteinuric kidney disease Part B: \- Completion of Treatment Period in Part A and no permanent discontinuation of study drug. Key Exclusion Criteria: Part A: * Solid organ or bone marrow transplant * Uncontrolled hypertension * History of diabetes mellitus * Known underlying cause of kidney disease including but not limited to sickle cell disease Part B: * ESKD (End Stage Kidney Disease) as defined in the protocol. * Any lab abnormality that may pose a safety risk to the participant, as judged by the investigator. Other protocol defined Inclusion/Exclusion criteria will apply.

Related Trials