跳至主要内容
临床试验/CTRI/2012/05/002676
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

ACTELION Pharmaceuticals Ltd0 个研究点目标入组 670 人开始时间: 待定最近更新:

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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