跳至主要内容
临床试验/NCT03899103
NCT03899103已完成3 期

Randomized Clinical Trial to Compare Efficacy and Safety of Repeated Courses of Rituximab to That of Maintenance Mycophenolate Mofetil Following Single Course of Rituximab in Maintaining Remission Over 24 Months Among Children With Steroid Dependent Nephrotic Syndrome

Nilratan Sircar Medical College1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2019年5月15日最近更新:
适应症
干预措施

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
100
试验地点
1
主要终点
The primary endpoint is the time to first relapse or death (whichever occurs first) till end of study (follow-up phase of 24 months)

研究概览

简要总结

The aim of the RITURNS II study is to evaluate the efficacy and safety of Repeat courses of Rituximab to that of maintenance Mycophenolate Mofetil following single course of Rituximab in maintaining remission over 24 months among Children with Steroid Dependent Nephrotic Syndrome (SDNS).

详细描述

The vast majority of children with idiopathic nephrotic syndrome respond well to corticosteroid treatment. However, as many as 70% experience at least one relapse, and 30% develop a more complicated course with frequent relapses (FRNS) with or without steroid dependency (SDNS). Extended steroid exposure in these children often results in long-term complications. The management of patients with SDNS is challenging and expensive. Relapses may lead to serious complications, e.g. related to anasarca, hypertension, life threatening infections (peritonitis, pneumonia, meningitis), thrombosis and malnutrition. Repeated courses or even continuous steroid treatment lead to considerable medication related toxicity and morbidity.

The goal of treatment is to reduce the rate of relapses, the cumulative dose of corticosteroids, and the incidence of serious complications. 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. Single rituximab infusion have been shown to be efficacious for 6 to 12 months and the side effect profile observed to date is very benign but after 6-8 months there was relapse due to regeneration of B-lymphocytes, hence for maintenance of remission MMF has been considered. In spite of good initial response, rituximab responders always remain prone to further relapse with regeneration of B lymphocytes, necessitating either repeat course of rituximab or addition of another steroid-sparing immunosuppressant. Reports suggest efficacy of rituximab may vary depending on disease pathology, clinical course, and simultaneous use of other immunosuppressants.

The aim of the RITURNS II study is to evaluate the efficacy and safety of Repeat courses of Rituximab to that of maintenance Mycophenolate Mofetil following single course of Rituximab in maintaining remission over 24 months among Children with Steroid Dependent Nephrotic Syndrome (SDNS).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
3 Years 至 16 Years(Child)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Repeated Courses of Rituximab Only

Experimental

First course Course Rituximab at Randomization. Prophylactic 2nd and 3rd course rituximab re-administration will be done at 8 months and 16 months of follow-up if B cell count normalize.

干预措施: Rituximab (Drug)

Rituximab and Mycophenolate Mofetil

Active Comparator

First course Course Rituximab at Randomization. Addition of Maintenance Mycophenolate Mofetil from 4 Month onwards.

干预措施: Rituximab (Drug)

Rituximab and Mycophenolate Mofetil

Active Comparator

First course Course Rituximab at Randomization. Addition of Maintenance Mycophenolate Mofetil from 4 Month onwards.

干预措施: Mycophenolate Mofetil (Drug)

结局指标

主要结局

The primary endpoint is the time to first relapse or death (whichever occurs first) till end of study (follow-up phase of 24 months)

时间窗: 24 months

次要结局

  • Number of relapses within months 0-24, 0-12 and 12-24, respectively(months 0-24, 0-12 and 12-24)
  • Cumulative prednisolone requirement (mg/kg/yr) over the first 12 and 24 months, respectively.(12 and 24 months)
  • Number and severity of adverse events(0-24 months)

研究者

发起方
Nilratan Sircar Medical College
申办方类型
Other Gov
责任方
Principal Investigator
主要研究者

Dr. Biswanath Basu

Associate Professor

Nilratan Sircar Medical College

研究点 (1)

Loading locations...

相似试验