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临床试验/NCT01815255
NCT01815255已完成不适用

Efficacy and Safety Evaluation of TDF-based Regimen in Thai HIV-infected Children

The HIV Netherlands Australia Thailand Research Collaboration2 个研究点 分布在 1 个国家目标入组 36 人开始时间: 2010年12月最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
36
试验地点
2
主要终点
viral load

研究概览

简要总结

This study will assess the safety and efficacy of generic TDF from Governmental Pharmaceutical Organization (GPO) in HIV-infected children

详细描述

TDF is a nucleotide reverse transcriptase inhibitor (NRTI) which can be taken only once per day and continues to have good efficacy even in patients who have resistance to other NNRTI in the absence of K65R mutation. TDF is a choice for patients with NRTI resistance, or those that require once-daily regimen to improve adherence. Currently, TDF has not been approved by the US FDA for children less than 18 years, but pediatricians has been using TDF in children who have treatment failure because of limitation of a more appropriate pediatric ARV. The Thai national guideline for pediatric 2009 recommend the use of TDF in children who have failed the first line therapy with multi-NRTI mutation and are more than 30 kilograms or have tanner stage 4 or more. However, the problem is that there is no pediatric TDF formulation. The available preparation of 300 mg tear drop tablet, if cut in half, may increase dosing errors, more or less by 18-37%. This will affect the blood level and/or toxicities. Therefore, the Thai Governmental Pharmaceutical Organization (GPO) has produced a generic TDF formulation that can be used in HIV-infected children. This study will assess the safety and efficacy information in children using this generic pediatric TDF formulation.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
8 Years 至 18 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • children who are changing to TDF due to adherence problem or treatment failure
  • children who are already on TDF due to their clinical indication

排除标准

  • child/caretaker refuse to participate in this study
  • cannot adhere to the study schedule

研究组 & 干预措施

tenofovir (TDF)

HIV-infected children who are currently on TDF-based regimen or are changing to TDF based on their clinical indication

干预措施: tenofovir (TDF) (Drug)

结局指标

主要结局

viral load

时间窗: week 48 and 96

Number of patients who have viral load less than 50 copies/ml at week 48 and week 96

次要结局

  • resistance(every 3 months)
  • adverse events(weeks 24, 48, 72, and 96)
  • renal status(weeks 24, 48, 72, and 96)
  • adherence(every 3 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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