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Clinical study on the efficacy and safety of tatacept in the treatment of idiopathic membranous nephropathy

Clinical study on the efficacy and safety of tatacept in the treatment of idiopathic membranous nephropathy

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200055179
Enrollment
Unknown
Registered
2022-01-02
Start date
2022-01-03
Completion date
Unknown
Last updated
2023-01-16

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

Conditions

Membranous nephropathy

Interventions

Sponsors

Qilu Hospital of Shandong University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Diagnosed with IMN by clinical and pathological examination; 2. Aged 18-70 years; 3. After 3 months or more of treatment with sufficient doses of ACEI or ARB and immunosuppressive agents; 24-hour proteinuria (UTP) >= 3.5g; 4. Stable blood pressure, =45ml/min/1.73m^2; 6. Agree to maintain stable diet and sodium intake during the study period; 7. Agree and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Unstable urine protein quantification in the last 2 months, 24-hour urine protein quantification fluctuation >2g/d; 2. Complicated with chronic liver disease, or liver enzymes more than 3 times the upper limit of normal; 3. New-onset cardiovascular and cerebrovascular diseases (acute coronary syndrome, heart failure, cerebral infarction, stroke) within 3 months; 4. Uncontrolled severe hypertension; 5. Malignant tumor; 6. Patients with severe infection; 7. Hypersensitivity or other contraindications to Taitacept; 8. During pregnancy or breastfeeding; 9. Life expectancy is less than 6 months; 10. Currently participating in other clinical studies; 11. Other circumstances that the researcher considers unsuitable to participate in this study.

Design outcomes

Primary

MeasureTime frame
24 urine protein;

Secondary

MeasureTime frame
eGFR;plasma albumin;drug side effects;

Countries

China

Contacts

Public ContactYang Xiangdong
yxd683@163.com+86 531 82169114

Outcome results

None listed

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