EUCTR2008-006833-29-IE进行中（未招募）不适用
An Open-Label Extension of BPS-MR-PAH-201 in Pulmonary Arterial Hypertension (PAH) Patients
ung LLC0 个研究点目标入组 19 人开始时间: 2008年12月11日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 19
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •Patients who remained on study drug and completed all assessements during the treatment phase of study BPS-MR-PAH-201 are eligible for this study.
- •Female Patients must either be physiologically incapable of childbearing or be practicing acceptable method of birth control (e.g approved hormonal contraceptive, barrier method, such as condom or diaphragm, used with a spemicide, or an intrauterine device
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 19
排除标准
- •Patients who discontinued study drug during the previous study (BPS-MR-PAH-201) for any reason (e.g. treatment related adverse event) are not eligible for entry into this study
- •Patients who are pregnant or lactating are excluded from participation in the open-label extension
研究者
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