跳至主要内容
临床试验/EUCTR2011-000437-36-DE
EUCTR2011-000437-36-DE进行中(未招募)1 期

A Phase IIb Randomized, Controlled, Partially-Blinded Trial to Investigate Safety, Efficacy and Dose-response of BMS-663068/GSK3684934 in Treatment-experienced HIV-1 Subjects, Followed by an Open-label Period on the Recommended Dose

ViiV Healthcare UK Limited0 个研究点目标入组 254 人开始时间: 2011年7月18日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
254

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

入选标准

  • Key inclusion criteria:
  • Plasma HIV-1 RNA = 1000 copies/ml
  • Men and women
  • At least 18 years of age, (or minimum age as determined by local regulatory or as legal requirements dictate, whichever is higher)
  • Antiretroviral treatment-experienced as defined in this protocol
  • Susceptibility to study drugs by genotype/phenotype/PhenoSense® Entry (AI)
  • CD4+ T-cell count > 50 cells/mm3
  • 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 250
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Key exclusion criteria:
  • Chronic HBV/HCV infection
  • Contraindications to any of study drugs
  • History of resistance to any component of the study regimen (TDF, ATV, RAL)

研究者

相似试验