Efficacy and Safety of Rituximab to That of Calcineurin Inhibitors in Children With Steroid Resistant Nephrotic Syndrome

Last updated: April 6, 2022
Sponsor: Nilratan Sircar Medical College
Overall Status: Active - Recruiting

Phase

4

Condition

Focal Segmental Glomerulosclerosis

Kidney Failure (Pediatric)

Nephropathy

Treatment

N/A

Clinical Study ID

NCT02382575
PednephroRCT/PM/NRSMCH-33
CTRI/2015/01/005364
  • Ages 3-16
  • All Genders

Study Summary

The vast majority of children with idiopathic nephrotic syndrome respond well to corticosteroid treatment. However, as many as 20% experience a more complicated course with steroid resistance (SRNS). Repeated and prolonged courses of steroids in these children often result in long-term complications. The goal of treatment is to reduce the rate of relapses, the cumulative dose of corticosteroids, and the incidence of serious complications. In order to minimize the side effects of steroid therapy, different steroid sparing agents such as cyclophosphamide, calcineurin inhibitors(CNI), levamisole, and mycophenolate mofetil (MMF) have been used in SRNS. Whereas CNI are usually considered the steroid sparing drug class of first choice, rituximab is increasingly used as alternative to minimize CNI toxicity. Various prospective studies suggest that Rituximab, a B cell depleting monoclonal antibody, could be a safe and effective alternative to steroid or immunosuppressants to achieve and maintain remission in this population. Rituximab infusion have been shown to be efficacious for 6 to 12 months and the side effect profile observed to date is very benign. Studies comparing the usefulness of these agents are lacking. In this proposed randomized controlled trial, the investigators want to compare the efficacy and safety of CNI to that of Rituximab in treating children with SRNS.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Children between 3 and 16 years with SRNS
  • Minimal Change disease/Messengioproliferative glomerulonephritis/Focal segmentalglomerulosclerosis as per Kidney Biopsy report.
  • Estimated glomerular filtration rate (eGFR) >80 ml/min per 1.73 m2 at study entry.
  • Not received any steroid sparing agent previously.
  • Parents willing to give informed written consent.
  • Ability to swallow tablet

Exclusion

Exclusion Criteria:

  • Known etiology (e.g., lupus erythematosus, IgA nephropathy, amyloidosis, malignancy,other secondary forms of NS)
  • Patients with severe leucopenia (leucocytes <3.0× 1000 cells/mm3), severe anemia (haemoglobin <8.9 g/dl), thrombocytopenia (platelet <100.0 × 1000 cells/mm3) orderanged liver function tests (AST or ALT to >50 IU/L ) at enrolment.
  • Known active chronic infection (tuberculosis, HIV, hepatitis B or C)
  • Live vaccination within 1 mo

Study Design

Total Participants: 120
Study Start date:
March 15, 2015
Estimated Completion Date:
December 31, 2023

Connect with a study center

  • NRS Medical College & Hospital

    Kolkata, West Bengal 700014
    India

    Active - Recruiting

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