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An Open-Label Phase 2 Study to Evaluate the Safety, Tolerability, and Effect on Albuminuria of MZE829 in Adults with Proteinuric Chronic Kidney Disease and the APOL1 High Risk Genotype


Description

This is purpose of this study is to evaluate the safety, tolerability, and effect on Albuminuria of MZE829 in Adults with APOL1 Kidney DiseaseAn open-label Phase 2 study is designed to evaluate the safety, tolerability, and effect on Albuminuria of MZE829 in Adults with Proteinuric Chronic Kidney Disease and the APOL1 High Risk Genotype.

Trial Eligibility

Key Inclusion Criteria: * APOL1 high risk genotype of G1/G1, G2/G2, or G1/G2 * Chronic kidney disease with persistent albuminuria Key Exclusion Criteria: * Organ or bone marrow transplantation * History of cancer within past 2 years, excepted for treated non-melanoma skin cancer, stage 0 cervical cancer, or stage 1 prostate cancer * Conditions that may alter drug absorption, e.g., history of bariatric surgery * Type I diabetes * Pregnant or currently nursing Other inclusion/exclusion criteria defined in protocol apply.

Study Info

Organization

Maze Therapeutics


Primary Outcome

Safety and tolerability as assessed by incidence of adverse events (AEs)


Outcome Timeframe Day 1 to Week 12

NCTID NCT06830629

Phases PHASE2

Primary Purpose TREATMENT

Start Date 2025-02-05

Completion Date 2026-09

Enrollment Target 56

Interventions

DRUG MZE829

Locations Recruiting

Apogee Clinical Research

United States, Alabama, Huntsville


Amicis Research Center

United States, California, Fairfield


Amicis Research Center

United States, California, Granada Hills


Amicis Research Center

United States, California, Palmdale


Amicis Research Center

United States, California, Valencia


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