The First Affiliated Hospital,Sun Yat-sen University
Guangzhou, Guangdong, China
NCT Number: NCT07555054
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 opening soon.
Get Notified18 year–70 year
All sexes
Interventional
Phase 2
Guangzhou, Guangdong, China
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
HS-10390
Target dose of 300 mg daily
Time frame: Frame: From baseline (Day 1) until Week 12 (Day 85)
Time frame: From baseline (Day 1) until Week 12 (Day 85)
Time frame: From baseline (Day 1) at each visit
Time frame: From baseline (Day 1) at Each Visit
Time frame: From baseline (Day 1) at Each Visit
Time frame: From baseline (Day 1) at Each Visit
Time frame: From screening until Follow-up visit (Day 98)
Contact information is provided by the study sponsor or research team.
Jiangsu Hansoh Pharmaceutical Co., Ltd.
Industry
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
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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