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临床试验/NCT00668356
NCT00668356暂停2 期

PKPOP Study of Didanosine in HIV Treated Children, at Fasting Period and During the Meal

Assistance Publique - Hôpitaux de Paris1 个研究点 分布在 1 个国家目标入组 26 人开始时间: 2009年9月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
暂停
入组人数
26
试验地点
1
主要终点
PK parameters

研究概览

简要总结

The purpose of this study is to show that the administration of 400/mg/m2/day of didanosine(ddI) during the meal is bioequivalent to the administration of 240/mg/m2/day of didanosine during fasting, in HIV infected children treated by a ARV combination including ddI

详细描述

The didanosine is one of the reverse transcriptase inhibitors. This drug is efficient against the viral replication of the HIV. Licensing for the children was obtained in June, 1992. The main problem of the didanosine is its poor bioavailability: although gastro-resistant capsules were developed, its bioavailability remains dependent on alimentation. Taking a meal 1-2 hours before the administration of ddI leads to a reduction of 50% of its bioavailability as well for the child as for the adult. It is therefore recommended to take ddI during fasting period. This regimen in some cases can decrease therapeutic observance. A pharmacokinetic study of ddI will be conducted during the meal with 240 mg/m2/day during fasting period compare to 400 mg/m2/day during the meal. 26 patients, aged more than 6 years old, will be included and randomised in 2 groups. The first group will take the standard dose of ddI during 28 days during fasting period (phase A), then the high dose during the meal during 28 days (phase B). The second group will take first the phase B and secondly the phase A. Patients will be sequentially evaluated both after the first and the second period of treatment for pharmacokinetics and biological analysis.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
6 Years 至 15 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Children treated by the didanosine capsules more than 3 months
  • viral load < 50 copies/ml
  • written informed consent
  • Normal renal function

排除标准

  • Lack of observance
  • Any treatments which can interact with ddI
  • No written informed consent
  • Weight > 60 kg

研究组 & 干预措施

1

Experimental

干预措施: didanosine (Drug)

2

Active Comparator

干预措施: didanosine (Drug)

结局指标

主要结局

PK parameters

时间窗: 28 days

次要结局

  • Biological analysis(28 days)
  • Quality of life(28 days)

研究者

申办方类型
Other

研究点 (1)

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