Efficacy and Safety of Obinutuzumab Versus Rituximab in Childhood Steroid Dependant and Frequent Relapsing Nephrotic Syndrome : a Double-blind Multicenter Randomized Controlled Study

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2/Phase 3
SUMMARY

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
Participation Requirements
Sex: All
Minimum Age: 3
Maximum Age: 18
Healthy Volunteers: f
View:

• Age between 3 and 18 years

• Steroid dependant Nephrotic Syndrome defined as:

‣ 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

∙ OR Frequent Relapsing Nephrotic Syndrome defined as:

• 2 or more relapses within 6 months following first remission

• 3 or more relapses within any 12-month period

‣ Last relapse within 3 months prior to inclusion

⁃ In remission, defined as 3 consecutive urinary dipsticks without proteinuria, at the time of randomization

⁃ Vaccination schedule in accordance with the current recommendations in France

⁃ Informed consent from parents

Locations
Other Locations
France
Robert Debre Hospital
RECRUITING
Paris
Contact Information
Primary
Claire DOSSIER, MD
claire.dossier@aphp.fr
+33140032467
Backup
Julien HOGAN, MD PhD
julien.hogan2@aphp.fr
+33140032142
Time Frame
Start Date: 2023-10-18
Estimated Completion Date: 2027-12-31
Participants
Target number of participants: 88
Treatments
Active_comparator: Rituximab 375 mg/m2
single infusion of Rituximab (375 mg/m2)
Experimental: Obinutuzumab 300 mg/1.73 m2
single infusion of Obinutuzumab 300 mg/1.73 m2
Related Therapeutic Areas
Sponsors
Leads: Assistance Publique - Hôpitaux de Paris

This content was sourced from clinicaltrials.gov