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Efficacy and Safety of Immunoglobulin Associated With Rituximab Versus Rituximab Alone in Childhood-Onset Steroid-dependent Nephrotic Syndrome

Phase 2
Suspended
Conditions
Steroid-Dependent Nephrotic Syndrome
Interventions
Drug: immunoglobulin IV
Registration Number
NCT03560011
Lead Sponsor
Assistance Publique - Hôpitaux de Paris
Brief Summary

Idiopathic Nephrotic Syndrome (INS) is the first glomerulopathy in children and 60% of the patients develop Steroid-Dependant Nephrotic Syndrome (SDNS). Recently, rituximab (RTX), a humanized anti-CD20 antibody depleting B cells demonstrated the ability to increase relapse free survival and to decrease the number of relapse and the need of other immunosuppressive drugs. However, the remission rate after 2 years is only 30 to 40%.

The aim of the study is to study the ability of intravenous Immunoglobulin to improve remission rate in SDNS when added associated with Rituximab compared to a treatment by Rituximab alone.

Detailed Description

Idiopathic Nephrotic Syndrome (INS) is the first glomerulopathy in children and 60% of the patients develop Steroid-Dependant Nephrotic Syndrome (SDNS). Depleting B cells demonstrated the ability to increase relapse free survival and to decrease the number of relapse and the need of other immunosuppressive drugs. However, the remission rate after 2 years is only 30 to 40%.

The aim of the study is to study the ability of intravenous Immunoglobulin to improve remission rate in SDNS when added associated with Rituximab compared to a treatment by Rituximab alone.

Recruitment & Eligibility

Status
SUSPENDED
Sex
All
Target Recruitment
90
Inclusion Criteria
  • Childhood onset nephrotic syndrome (first flair <18 years)

  • ≥ 2 years old at inclusion

  • Steroid-dependent:

    • Patient with at least 2 relapses confirmed during the decay of corticosteroids or within 2 weeks following steroids discontinuation.
    • Patient with at least 2 relapses including one under steroidsparing agent (MMF, Calcineurin inhibitors, cyclophosphamide, Levamisole) or within 6 months of treatment withdrawal.
  • or with frequent relapses:

    · 2 or more relapses within 6 months after initial remission or 4 or more relapses within any 12-month period.

  • with a relapse within 3 months prior to inclusion

  • In remission: Protein-over-creatinine ratio ≤ 0.2g/g (≤ 0.02g/mmol)

Exclusion Criteria
  • Patients with steroid-resistant nephrotic syndrome;
  • Patients with genetic nephrotic syndrome;
  • Patients previously treated with rituximab;
  • Patients with no affiliation to a social security scheme (beneficiary or legal);
  • Prior Hepatitis B, Hepatitis C or HIV infection;
  • Pregnancy or breastfeeding.
  • Patients with hyperprolinaemia,
  • Known hypersensitivity to one of the study medication,
  • Scheduled and not postponable injection of live attenuated vaccine
  • Protected adults
  • Patients with neutrophils < 1.5 G/L and/or platelets < 75 G/L

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Rituximab followed by 5 injections of immunoglobulin IVimmunoglobulin IVRituximab (375 mg/m²) followed by 5 injections of immunoglobulin IV once a month during 5 months (2g/kg at M1, 1.5g/kg at M2 to M5, maximal dose 100g). Treatment duration : 6 months
Primary Outcome Measures
NameTimeMethod
The occurrence of the first relapse24 months

Relapse is defined as a protein to creatinine ratio of 2g/g of creatinine (0.2 g/mmol) or higher

Secondary Outcome Measures
NameTimeMethod
Time to first relapse24 months
Number of relapse over a 24 months follow-up24 months
Cumulative amount of corticosteroid over a 24 months follow-up24 months
Adverse events in each arm24 months

Trial Locations

Locations (1)

Robert Debre Hospital

🇫🇷

Paris, France

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