跳至主要内容
临床试验/EUCTR2012-004411-31-GR
EUCTR2012-004411-31-GR进行中(未招募)1 期

ong term, single-arm, open-label extension study of protocol AC-055-305 to assess the safety, tolerability and efficacy of macitentan in subjects with Eisenmenger Syndrome - MAESTRO-OL: MAcitentan in Eisenmenger Syndrome To RestOre exercise capacity (Open-Label)

Actelion Pharmaceuticals Ltd.0 个研究点目标入组 220 人开始时间: 2015年4月29日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
220

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

  • Subjects with ES (including those with Down Syndrome [DS]) having completed the double-blind AC-055-305 / MAESTRO study as scheduled, i.e., who remained in the double-blind study up to Week 16 (whether or not they were still taking study drug at the end of this period).
  • Are the trial subjects under 18? yes
  • Number of subjects for this age range: 15
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 190
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 15

排除标准

  • Subjects who prematurely discontinue double-blind study drug during the AC-055-305 / MAESTRO study due to:
  • - an adverse event (AE) assessed as related to the use of study drug, or
  • - elevated liver tests (LTs; related or unrelated to study drug)

研究者

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