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临床试验/EUCTR2004-004917-41-IT
EUCTR2004-004917-41-IT进行中(未招募)不适用

A prospective, randomized, double-blind, active controlled, parallel group, multi-center trial to assess the efficacy and safety of mycophenolate mofetil MMF in inducing response and maintaining remission in subjects with lupus nephritis

ASPREVA PHARMACEUTICALS CORPORATIO0 个研究点目标入组 358 人开始时间: 2007年2月1日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
358

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • Are the trial subjects under 18? yes
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • 未提供

研究者

发起方
ASPREVA PHARMACEUTICALS CORPORATIO

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