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NOT YET RECRUITING
NCT07555054
PHASE2

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.

View on ClinicalTrials.gov

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

Interventions

DRUG

HS-10390

HS-10390

DRUG

HS-10390

HS-10390

DRUG

HS-10390

HS-10390

DRUG

Irbesartan

Target dose of 300 mg daily

Locations (1)

The First Affiliated Hospital,Sun Yat-sen University

Guangzhou, Guangdong, China