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临床试验/EUCTR2010-023946-58-NL
EUCTR2010-023946-58-NL进行中(未招募)不适用

Immunogenicity and safety of an adjuvant hepatitis B vaccine (fendrix) compared to Engerix in non-responding HIV-infected patients

ErasmusMC0 个研究点开始时间: 2011年1月31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

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

  • Eligible patients must be on HAART, with HIV-RNA < 200 copies/ml and CD4+-cell counts > 200/ml and negative HBsAg, anti-HBc and anti-HBs titers.
  • Are the trial subjects under 18? no
  • 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

  • Exclusion criteria
  • -co-infection with hepatitis C
  • -pregnancy
  • -radiation therapy
  • -cytotoxic agents
  • -any immunemodulator

研究者

发起方
ErasmusMC

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