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临床试验/JPRN-UMIN000027674
JPRN-UMIN000027674已完成1 期

A pharmacokinetic study of sodium phenylbutyrate in healthy adults for refractory pediatric cholestatic disease's therapy - A pharmacokinetic study of sodium phenylbutyrate in healthy adults

Juntendo University0 个研究点目标入组 20 人开始时间: 2017年6月7日最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
入组人数
20

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

年龄范围
20years-old 至 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1) Those who have hypersensitivity with phenylbutylate, its metabolites, drug additives and/or benzoate, etc. 2) Those who have experienced serious disease. 3) Those who have received medication in the previous two months. 4) Those who have received more than 200ml whole blood sampling in the previous 4 weeks, or blood component sampling in the previous 2 weeks. 5) Those who have received more than 400ml whole blood sampling in the previous 12 weeks. 6) Those who have been included in any phase 1 clinical trial for medicine containing new active ingredient in the previous 4 months. 7) Those who are less than 20 years old. 8) Drug addicts. 9) Alcoholics 10) Those who have been determined ineligible by principal investigator or sub-investigator.

研究者

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