Clinical Trial

A Study of the Effect and Safety of HS-10390 in the Treatment of Participants With Chronic Kidney Disease

Not Yet Recruiting Phase 2
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Summary
The purpose of the study was to evaluate the efficacy and safety of HS-10390 in participants with chronic kidney disease (CKD) with estimated glomerular filtration rate (eGFR) ≥ 30 and \<90 mL/min/1.73 m\^2, and urinary albumin to creatinine ratio (UACR) ≥ 150 mg/g and \< 3000 mg/g
Trial Details
NCT Number NCT07555054
Lead Sponsor Jiangsu Hansoh Pharmaceutical Co., Ltd.
Conditions Chronic Kidney Disease
Enrollment 182 participants
Start Date 2026-05-21
Primary Completion 2027-11-11 (estimated)
Study Completion 2028-12-31 (estimated)
Updated on ClinicalTrials.gov 2026-04-28