Last updated: November 8, 2023
Sponsor: Assistance Publique - Hôpitaux de Paris
Overall Status: Active - Recruiting
Phase
2/3
Condition
Focal Segmental Glomerulosclerosis
Nephrotic Syndrome
Nephropathy
Treatment
single infusion of Obinutuzumab
single infusion of Rituximab
Clinical Study ID
NCT05786768
APHP211038
2022-003336-59
Ages 3-18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- 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, Calcineurininhibitors, cyclophosphamide, levamisole) or within 6 months following treatmentwithdrawal 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, atthe time of randomization
- Vaccination schedule in accordance with the current recommendations in France
- Informed consent from parents
Exclusion
Exclusion Criteria:
- Secondary cause of nephrotic syndrome (such as membranous nephropathy, IgAnephropathy, lupus nephritis)
- Primary or secondary steroid resistance nephrotic syndrome
- Prior treatment with Rituximab within 6 months
- Prior treatment with obinutuzumab at any time
- CD20+ B-cell count < 2.5%
- Patient with neutrophils < 1.5 G/L and/or platelets < 75 G/L
- GFR < 80 ml/min/1.73m2
- Weight <16kg
- History of severe infection such as tuberculosis, hepatitis B, hepatitis C or HIVinfection or LEMP
- History of malignancy- Uncontrolled infection (viral, bacterial and fungal)
- Vaccination with a live vaccine within 4 weeks prior to assignment/randomization
- Known hyperprolinemia
- Hypersensitivity to the active substance (OBI or RTX) or to proteins of murine origin,or to any of the other excipients
- Pregnancy or breastfeeding or ability to become pregnant and refusal to use effectivecontraception during the 18 months following the study treatment (only 1 infusion ofobinutuzumab/Rituximab at the beginning of the study)
- Patient without medical insurance coverage (beneficiary or legal)
Study Design
Total Participants: 88
Treatment Group(s): 2
Primary Treatment: single infusion of Obinutuzumab
Phase: 2/3
Study Start date:
October 18, 2023
Estimated Completion Date:
December 31, 2027
Study Description
Connect with a study center
Robert Debre Hospital
Paris, 75019
FranceActive - Recruiting
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