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A Study of the Effect and Safety of HS-10390 in the Treatment of Participants With Chronic Kidney Disease
Sponsor: Jiangsu Hansoh Pharmaceutical Co., Ltd.
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
Official title: A Randomized, Multicenter, Double-blind, Parallel Active-control Study of the Efficacy and Safety of HS-10390 for the Treatment of Participants With Chronic Kidney Disease
Key Details
Gender
All
Age Range
18 Years - 70 Years
Study Type
INTERVENTIONAL
Enrollment
182
Start Date
2026-05-21
Completion Date
2028-12-31
Last Updated
2026-04-28
Healthy Volunteers
No
Conditions
Interventions
HS-10390
HS-10390
HS-10390
HS-10390
HS-10390
HS-10390
Irbesartan
Target dose of 300 mg daily
Locations (1)
The First Affiliated Hospital,Sun Yat-sen University
Guangzhou, Guangdong, China