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
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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