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
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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