跳至主要内容
临床试验/CTRI/2009/091/000183
CTRI/2009/091/000183Other3 期

A Phase 3, Multi-Center, Open Label Study To Evaluate The Long-Term Safety Of Monotherapy Sitaxsentan Sodium And Combination Therapy With Sitaxsentan Sodium And Sildenafil Citrate In Subjects With Pulmonary Arterial Hypertension. - Not applicable

Pfizer Limited0 个研究点目标入组 180 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
Other
入组人数
180

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

入选标准

  • Ages Eligible for Study: 16 Years to 80 Years
  • Genders Eligible for Study: Both
  • Accepts Healthy Volunteers: No
  • Previously enrolled in B1321001 for at least 4 weeks.
  • Previously enrolled in B1321003, discontinued from the study.
  • Completed the B1321003 study as planned.

排除标准

  • Treated with an investigational drug (other than sitaxsentan or sildenafil in either B1321001 or B1321003) or device that has not received regulatory approval within the 30 days prior to Baseline/Day 1 or during the study.

研究者

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