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Exploration of the Efficacy and Safety of Finerenone in the Treatment of Membranous Nephropathy

Exploration of the Efficacy and Safety of Finerenone in the Treatment of Membranous Nephropathy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500103410
Enrollment
Unknown
Registered
2025-05-29
Start date
2025-06-01
Completion date
Unknown
Last updated
2025-06-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Membranous Nephropathy

Interventions

Intervention group:Maximum tolerable dose of ACEI/ARB and finerenone 20 mg QD
Control group:Maximum tolerable dose of ACEI/ARB

Sponsors

General Hospital of Ningxia Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Older than 18 years of age; 2. Diagnosed with membranous nephropathy, with eGFR > 60 mL/min/1.73 m2, and UACR 30-5000mg/g; 3. Receiving a stable maximum tolerated dose of ACEi or ARB for at least 4 weeks.

Exclusion criteria

Exclusion criteria: 1. Diagnosed with type 1 or type 2 diabetes; 2. Any other primary or secondary kidney disease, receiving hormone, immunosuppressant treatment within 3 months prior to screening, or biological agents within 6 months; 3. Severe liver damage and heart failure; active malignancy, pregnancy, history of organ transplantation, etc. 4. Unable to discontinue the use of eplerenone, spironolactone, esaxerenone, or potassium-sparing diuretics within 4 weeks prior to enrollment.

Design outcomes

Primary

MeasureTime frame
Urine Albumin-to-Creatinine Ratio, UACR;

Secondary

MeasureTime frame
24-hour urine protein;Estimated Glomerular Filtration Rate;

Countries

China

Contacts

Public ContactXiaoling Zhou

General Hospital of Ningxia Medical University

zxlingsky@163.com+86 138 9507 8577

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026