drugset / Trial / NCT04531865

Randomized Trial Evaluating Mycophenolate Mofetil in Children With Nephrotic Syndrome After Rituximab Treatment

NCT04531865

RandomizedParallel-groupQuadruple-blindTreatment

Summary

The aim of this study is to evaluate the efficacy and safety of maintenance Mycophenolate Mofetil following single course of Rituximab in maintaining remission over 12 months among Children with frequently-relapsing or steroid-dependent nephrotic syndrome

Timeline

Start
2021-01-01
Primary completion
2022-09-01
Completion
2022-10-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Mycophenolate Mofetil Small molecule 20 mg/kg
Subject Mycophenolate Mofetil Small molecule 30 mg/kg
Background Rituximab Monoclonal antibody 375 mg/m2 Intravenous

Indications