跳至主要内容
临床试验/EUCTR2012-001142-18-NL
EUCTR2012-001142-18-NL进行中(未招募)不适用

Efficacy and pharmacokinetics of a switch from a regimen consisting of emtricitabine, nevirapine and tenofovir to rilpivirine, emtricitabine and tenofovir in virologically suppressed HIV-1 infected patients. - rilpivirine switch study

Erasmus MC0 个研究点目标入组 50 人开始时间: 2012年8月30日最近更新:
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
Erasmus MC
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

  • Able to take medication with a 500 kcal meal.
  • Treated with NVP, FTC, TDF for at least the last 9 months.
  • No history of HIV virologic failure.
  • The last 2 measured HIV-RNA levels in plasma were <50 copies/ml.
  • =6 months between the first and last plasma with <50 copies/ HIV RNA/ml.
  • 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 50
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Use of proton pump inhibitors.
  • Use of H2-antagonists.

研究者

发起方
Erasmus MC

相似试验