This study will evaluate the efficacy and safety of HR19042 capsules compared to matching placebo for the treatment of primary IgA nephropathy, and explore the optimal dose for the treatment.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
316
HR19042 Capsules
Placebo
NanFang Hospital of Southern Medical University
Guangzhou, Guangdong, China
Change from baseline in urine protein creatinine ratio (UPCR)
Time frame: 9 months
Change from baseline in 24-hour proteinuria
Time frame: 9 months
Change from baseline in urine albumin creatinine ratio (UACR)
Time frame: 9 months
Change from baseline in estimated GFR
Time frame: 9 months
Change from baseline in estimated GFR
Time frame: 12 months
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