跳至主要内容
临床试验/NL-OMON39075
NL-OMON39075已完成3 期

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 Pharmaceuticals0 个研究点目标入组 5 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
5

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

年龄范围
18 至 99(—)

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

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

发起方
Actelion Pharmaceuticals

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