This is purpose of this study is to evaluate the safety, tolerability, and effect on Albuminuria of MZE829 in Adults with APOL1 Kidney Disease
An 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.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
56
Capsules for oral administration
Safety and tolerability as assessed by incidence of adverse events (AEs)
Time frame: Day 1 to Week 12
Percent participants with ≥30% reduction from baseline in UACR at Week 12
Time frame: Day 1 to Week 12
Geometric mean plasma drug concentrations
Time frame: Day 1 to Week 12
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Research Site
Decatur, Alabama, United States
RECRUITINGResearch Site
Huntsville, Alabama, United States
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Montgomery, Alabama, United States
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Granada Hills, California, United States
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Bloomfield, Connecticut, United States
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Atlantis, Florida, United States
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Brandon, Florida, United States
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Brooksville, Florida, United States
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Hollywood, Florida, United States
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Melbourne, Florida, United States
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