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NCT Number: NCT07555054

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

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

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Key information

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

The First Affiliated Hospital,Sun Yat-sen University

Guangzhou, Guangdong, China

Location contact

Wei Chen WC archiater, Doctor

CONTACT

[email protected]

13924150966

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Men and women aged 18-70 years old;
  • Body mass index (BMI) ≥18.0 and <50.0 kg/m^2 at screening;
  • Currently on stable dose (maximum tolerated dose and at least one-half of the maximum labeled dose) of ACEI and/or ARB therapy for at least 4 weeks and treated for at least 3 months prior to the screening visit;
  • Diagnosed with chronic kidney disease, and the estimated glomerular filtration rate (eGFR) was ≥30 and <90 mL/min/1.73 m^2 calculated using the 2021 CKD-EPI creatine formula at screening;
  • Urinary albumin/creatinine ratio (UACR) was ≥300 and <3000 mg/g for at least 2 times on different days detected by the local laboratory at screening;
  • Systolic BP between 90 and 160 mmHg and diastolic BP between 60 and 100 mmHg;
  • Agree to contraception.

Exclusion criteria

  • A known or suspected allergy to the investigational medical drug or its components or excipients;
  • Within 4 weeks before screening, the following drugs could not maintain the stable regimen: diabetes drugs, hypertension drugs, non-steroidal anti-inflammatory drugs;
  • If glucagon-like peptide-1 receptor agonists (GLP-1 RAs) are prescribed, the dose are unstable within 8 weeks before screening ;
  • Participants with uncontrolled diabetes mellitus (HbA1c > 8%);
  • Received any other study drug treatment within 30 days or 5 half-lives (whichever is longer) prior to screening;
  • Polycystic kidney disease, lupus nephritis, anti-neutrophil cytoplasmic antibody (ANCA) -associated vasculitis, acute glomerulonephritis, bilateral renal artery stenosis;
  • Acute kidney injury or dialysis treatment within 6 months before screening;
  • Received kidney transplant, or plan to receive kidney transplant during the trial;
  • Platelet< 100×10^9/L or hemoglobin value < 90 g/L or Hematocrit value < 27% (0.27 V/V) at screening;
  • Elevations of transaminases (ALT and/or AST) >3 times upper limit of normal (ULN) or total bilirubin exceeding 1.5 times the upper limit of normal at screening;
  • Serum potassium >5.5 mmol/L at screening.

Treatment and study plan

HS-10390

Drug

HS-10390

Irbesartan

Drug

Target dose of 300 mg daily

Primary outcomes

  1. Change in Urinary Albumin to Creatinine Ratio (UACR) From Baseline to Week 12

    Time frame: Frame: From baseline (Day 1) until Week 12 (Day 85)

Secondary outcomes

  1. Proportion of participants achieving ≥20%, ≥30%, and ≥40% reduction in UACR from baseline at week 12

    Time frame: From baseline (Day 1) until Week 12 (Day 85)

  2. Change in Urine Protein/Creatinine Ratio (UPCR) From Baseline at Each Visit

    Time frame: From baseline (Day 1) at each visit

  3. Change in 24 hour Urinary Protein Excretion From Baseline at Each Visit

    Time frame: From baseline (Day 1) at Each Visit

  4. Change in Estimated Glomerular Filtration Rate (eGFR) From Baseline at Each Visit

    Time frame: From baseline (Day 1) at Each Visit

  5. Change in Office Systolic and Diastolic Blood Pressure From Baseline at Each Visit

    Time frame: From baseline (Day 1) at Each Visit

  6. Number of Participants With Adverse Events (AE) and Serious Adverse Events (SAE)

    Time frame: From screening until Follow-up visit (Day 98)

Study contacts

Contact information is provided by the study sponsor or research team.

Wei Chen Professor, MD

CONTACT

[email protected]

13924150966

Sponsors and collaborators

Lead sponsor

Jiangsu Hansoh Pharmaceutical Co., Ltd.

Industry

Registry information

Official study 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

Important dates

Study start
2026
Primary completion
2027
Study completion
2028
First posted
Apr 28, 2026
Registry last updated
Apr 28, 2026

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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