About this trial
B-cell depletion with rituximab induces sustained remission in children with Steroid-Dependent or Frequent Relapsing Nephrotic Syndrome (SD/FRNS). However, most patients relapse after B-cell recovery and some do not achieve B-cell depletion. Obinutuzumab is a 2nd generation humanized monoclonal antiCD20 antibody, with enhanced B cell-depleting potential. It has been reported safe and efficient in different renal autoimmune diseases including childhood nephrotic syndrome. This double-blind, randomized multicenter study is designed to assess the efficacy and safety of a single infusion of low-dose obinutuzumab compared to a single infusion of rituximab in children with frequently relapsing nephrotic syndrome (FRNS) or steroid-dependent nephrotic syndrome (SDNS).
Eligibility criteria
Qualifiers
Age between 3 and 18 years
2 or more relapses during steroids or within 2 weeks following discontinuation.
2 or more relapses including one under steroid-sparing agent (MMF, Calcineurin inhibitors, cyclophosphamide, levamisole) or within 6 months following treatment withdrawal
2 or more relapses within 6 months following first remission
Disqualifiers
Secondary cause of nephrotic syndrome (such as membranous nephropathy, IgA nephropathy, lupus nephritis)
Primary or secondary steroid resistance nephrotic syndrome
Prior treatment with Rituximab within 6 months
Prior treatment with obinutuzumab at any time
Trial design
Treatments tested in this trial
- single infusion of Rituximab
- single infusion of Obinutuzumab