CTRI/2017/09/009938进行中（未招募）4 期
Management using the Latest Technologies in Resource-Limited Settings to Optimize Combination Therapy after Viral Failure (Multi-OCTAVE) - MULTIOCTAVE
ational Institute Of Allergy and Infectious DiseasesNIAIDNIH0 个研究点目标入组 100 人开始时间: 待定最近更新:
试验速览
- 阶段
- 4 期
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 100
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
入选标准
- •NOTE: All potential participants with prior RAL exposure will be assigned to Cohort D.
- •3.Current receipt of a PI-based regimen with no regimen change for a minimum of 24 weeks prior to screening.
- •NOTE A: Within the 30 days prior to collection of the confirmatory VF sample (see 4.1.4), alteration in dose, dose frequency, or any within-class substitution(s) for intolerance is permitted, as are drug interruptions for fewer than 7 cumulative days.
- •NOTE B: There can be no changes and no drug interruptions within the 3 days immediately prior to the collection of the confirmatory VF sample
排除标准
- •Contraindication to the proposed Step 2 ARV regimen as determined by the site investigator.
- •Indication for discontinuation of RAL, ETR, or DRV.
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