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