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A single-center prospective study of rituximab in the treatment of adult refractory nephrotic syndrome

A single-center prospective study of rituximab in the treatment of adult refractory nephrotic syndrome

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000031963
Enrollment
Unknown
Registered
2020-04-16
Start date
2020-07-01
Completion date
Unknown
Last updated
2021-01-05

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

Conditions

Adult refractory nephrotic syndrome

Interventions

experimental group:Rituximab treatment
contol group: routine regimen

Sponsors

???
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients diagnosed as primary nephrotic syndrome (MCD, IMN, FSGS); 2. Patients older than 18 years old; 3. EGFR > 40ml / min, urinary protein > 3.5g/d; 4. In patients who received traditional treatment for at least 3 months (glucocorticoid, immunosuppressant CNI (tacrolimus or cyclosporine A), ACEI), the urinary protein decreased by less than 50%.

Exclusion criteria

Exclusion criteria: 1. Patients with a history of RTX use; 2. Patients with hepatitis B, hepatitis C, HIV, etc; 3. Patients allergic to the drug or mouse protein; 4. Patients with severe active infection; 5. Patients with severe impairment of immune response (such as hypogammaglobulinemia, severe CD4 or CD8 cell count reduction); 6. Patients with severe heart failure (NYHA grade IV); 7. Those who are pregnant, nursing, or using unreliable methods of contraception.

Design outcomes

Primary

MeasureTime frame
Disease remission;

Countries

China

Contacts

Public ContactQijun Wan

Department of Endocrinology, Shenzhen Second People’s Hospital,

yiyuan2224@sina.com+86 13537857368

Outcome results

None listed

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