跳至主要内容
临床试验/JPRN-jRCT2080222108
JPRN-jRCT2080222108未知3 期

Open-label, multicenter study to assess the efficacy, safety, tolerability, and pharmacokinetics of bosentan in Japanese children with pulmonary arterial hypertension

Actelion Pharmaceuticals Japan Ltd.0 个研究点目标入组 5 人开始时间: 2013年6月11日最近更新:
适应症

试验速览

阶段
3 期
发起方
入组人数
5

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
ot applicable 至 <= 14age old(—)
性别
All

入选标准

  • Idiopathic PAH, Heritable PAH, PAH associated with CHD

排除标准

  • Co-exisiting hepatic impairment etc.

研究者

发起方
Actelion Pharmaceuticals Japan Ltd.

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