CTRI/2012/05/002676招募中3 期
ong-term single-arm open-label study, to assess the safety and tolerability of ACT-293987 in patients with pulmonary arterial hypertension - GRIPHON O
试验速览
- 阶段
- 3 期
- 状态
- 招募中
- 入组人数
- 670
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
- •Patients who have completed the double-blind study AC-065A302 as scheduled per protocol (i.e., treated until unblinding of the study), or who have experienced a clinical worsening of PAH (adjudicated by the CEC) during study AC-065A302.
- •Signed informed consent
排除标准
- •Any major violation of protocol AC-065A302.
- •Females who plan to become pregnant during the study, or are breastfeeding.
- •Any known factor or disease that might interfere with treatment compliance, study conduct or interpretation of the results, such as drug or alcohol dependence, or psychiatric disease.
- •Known hypersensitivity to ACT-293987 or any of the excipients.
研究者
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