跳至主要内容
临床试验/EUCTR2012-001970-28-GB
EUCTR2012-001970-28-GB进行中(未招募)不适用

Does CMV reactivation cause functional impairment of CMV specific CD4+ T-cells? The potential for valaciclovir to prevent CMV-mediated adverse modulation of the immune system in patients with ANCA-associated vasculitis - CMV modulation of the immune system in ANCA-associated vasculitis - v1

niversity of Birmingham0 个研究点目标入组 50 人开始时间: 2012年10月10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)
入组人数
50

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

  • Documented diagnosis of ANCA associated vasculitis
  • In stable remission (no documented clinical disease activity) for at least 6 months prior to entry.
  • On maintenance immunosuppression with maximum 2 agents.
  • Documented evidence of CMV infection.
  • Documentation that female patients of child bearing age are not pregnant.
  • Written informed consent for study participation
  • Are the trial subjects under 18? no
  • Number of subjects for this age range: 0
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 25
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 25

排除标准

  • Severe chronic kidney disease (Stage 5).
  • Other significant chronic infection (HIV, HBV, HCV, TB).
  • B-cell or T-cell depleting therapy within 12 months.
  • Treatment with anti-CMV therapies in last month
  • Underlying medical conditions, which in the opinion of the Investigator place the patient at unacceptably high risk for participating in the study.
  • Inability to fully or appropriately participate in the study.

研究者

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