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临床试验/NL-OMON32184
NL-OMON32184已完成3 期

A Phase III, randomized, double-blind study of TMC278 75 mg q.d. versus efavirenz 600 mg q.d. in combination with a fixed background regimen consisting of tenofovir disoproxil fumarate and emtricitabine in antiretroviral-naïve HIV-1 infected subjects. - SPRINT : Simplified Pill Regimen In Naive patients with TMC278

Janssen-Cilag0 个研究点目标入组 12 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
发起方
Janssen-Cilag
入组人数
12

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 99(—)

入选标准

  • Male or female subjects, aged 18 years or older;
  • Subject with documented HIV-1 infection;
  • Subject has never been treated with a therapeutic HIV vaccine or an ARV drug prior to screening;
  • HIV-1 plasma viral load at screening is >= 5,000 HIV-1 RNA copies/mL

排除标准

  • Any previous treatment with a therapeutic HIV vaccine or use of ARVs, including use of NVP for the prevention of vertical HIV transmission;
  • Having documented genotypic evidence of NNRTI resistance at screening;
  • Previously documented HIV-2 infection;
  • Subject has any currently active AIDS defining illness (with a few exceptions).

研究者

发起方
Janssen-Cilag

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