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Obinutuzumab in the treatment of RTX-resistant adult primary membranous nephropathy

Obinutuzumab in the treatment of RTX-resistant adult primary membranous nephropathy:A multi-center prospective study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400083188
Enrollment
Unknown
Registered
2024-04-17
Start date
2024-04-17
Completion date
Unknown
Last updated
2024-04-22

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

Conditions

membranous nephropathy

Interventions

Obinutuzumab group:Obinutuzumab

Sponsors

The Second People's Hospital of Shenzhen
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1.Age =18 years ; 2.Primary membranous nephropathy diagnosed by renal biopsy; 3.Resist to Rituximab treatment : no remission of urinary protein after the use of RTX ( 1g / time, 2 times / course , interval of 2 weeks ) after 9 months ; or ARA positive ; 4.No hormone or other immunosuppressive agents were used within 12 months; 5.Estimated glomerular filtration rate ( GFR ) = 30 mL / min / 1.73 m2; 6. Sign informed consent before medication.

Exclusion criteria

Exclusion criteria: 1.There are secondary causes of membranous nephropathy ( including special infections such as active hepatitis, active tuberculosis, rheumatic immune system diseases such as SLE, malignant tumor or MN caused by drug factors ) ; 2.Serum creatinine > 2.0 mg / dL or estimated GFR < 30 mL / min / 1.73 m2 ; 3.There are complications of nephrotic syndrome such as active infection, acute kidney injury and thromboembolism; 4.Pregnancy status or plan to conceive or lactation women.

Design outcomes

Primary

MeasureTime frame
remission rate;

Secondary

MeasureTime frame
Recurrence rate;Renal prognosis;

Countries

China

Contacts

Public ContactLiu Yang

The First Affiliated Hospital of Shenzhen University (the Second People's Hospital of Shenzhen)

lyangnjhu@163.com+86 186 6456 0737

Outcome results

None listed

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