跳至主要内容
临床试验/EUCTR2006-006437-40-IT
EUCTR2006-006437-40-IT进行中(未招募)不适用

Randomised, controlled open label trial to compare the efficacy safety and tolerability of a treatment simplification by darunavir/ritonavir DRV/r 800/100 mg OD vs a triple combination therapy containing DRV/r in HIV-1 infected subjects with undetectable plasma HIV-1 RNA on their current treatments - TMC114HIV3006

JANSSEN-CILAG INTERNATIONAL N.V.0 个研究点目标入组 250 人开始时间: 2007年4月24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
250

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 HIV infection Male and female subjects aged 18 or older ICON voluntarily signed HAART therapy ongoing for 24 weeks HIV-1 RNA plasma 50 copies/ml for at least 24 weeks prior to screening
  • 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

  • History of virological failure defined as two consecutive plasma HIV-1 RNA 500 copies per ml while on previous or current ARV therapy History of any primary PI mutations as defined in IAS-USA guideline 2006

研究者

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