跳至主要内容
临床试验/JPRN-jRCT2080221626
JPRN-jRCT2080221626未知2 期

An exploratory study to assess the efficacy and safety of NS-304 in patients with chronic thromboembolic pulmonary hypertension (CTEPH)

IPPON SHINYAKU CO., LTD. / Actelion Pharmaceuticals Japan Ltd.0 个研究点目标入组 32 人开始时间: 2011年10月18日最近更新:
适应症

试验速览

阶段
2 期
发起方
入组人数
32

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
>= 20age old 至 <= 75age old(—)
性别
All

入选标准

  • CTEPH patient as demonstrated the deficit of lung perfusion by ventilation/perfusion lung scanning and pulmonary angiography

排除标准

  • 未提供

研究者

发起方
IPPON SHINYAKU CO., LTD. / Actelion Pharmaceuticals Japan Ltd.

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