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临床试验/EUCTR2010-018320-10-NL
EUCTR2010-018320-10-NL进行中(未招募)不适用

An open-label extension of study AC-066A301 investigating the safety and tolerability of ACT-385781A in patients with pulmonary arterial hypertension (PAH) - EPITOME-2 Extension

ACTELION Pharmaceuticals Ltd0 个研究点目标入组 40 人开始时间: 2011年5月12日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
40

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

  • 1. Signed informed consent prior to initiation of any study mandated procedure
  • 2. Patients who completed participation in study AC 066A301
  • 3. Patients who have not obtained access (i.e. reimbursement) to commercial EFI at the time of ending participation in study AC-066A301
  • 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 36
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 4

排除标准

  • 1. Patients who prematurely discontinued study drug in study AC-066A301
  • 2. Patients for whom continued treatment with EFI is no longer considered appropriate

研究者

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