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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)
Interventions
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
Interested in joining this trial?
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