跳至主要内容
临床试验/JPRN-jRCT2080221333
JPRN-jRCT2080221333未知3 期

A Phase 3, Multi-Center, Open Label Study To Evaluate The Long-Term Safety Of Sitaxentan Sodium In Japanese Subjects With Pulmonary Arterial Hypertension

Pfizer Japan Inc.0 个研究点目标入组 35 人开始时间: 2010年12月9日最近更新:
适应症

试验速览

阶段
3 期
入组人数
35

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
>= 16age old 至 <= 80age old(—)
性别
All

入选标准

  • Subject who completed the B1321052 study as planned

排除标准

  • 1.Has uncontrolled systemic hypertension as evidenced by sitting systolic blood pressure >160 mm Hg or sitting diastolic blood pressure >100 mm Hg at Screening
  • 2.Has hypotension defined as systolic arterial pressure <90 mm Hg after sitting for 5 minutes at Screening.

研究者

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