跳至主要内容
临床试验/EUCTR2009-018267-27-ES
EUCTR2009-018267-27-ES进行中(未招募)不适用

A 5-Year, Extension, Follow-up, Blinded-Outcomes Trial of Subjects Having Received Stannsoporfin or Placebo in Clinical Trial 64,185-202Un estudio ciego de seguimiento y ampliación de 5 años de duración de pacientes que recibieron estansoporfina o placebo en el ensayo clínico 64.185-202

InfaCare Pharmaceutical Corporation0 个研究点目标入组 72 人开始时间: 2010年1月22日最近更新:

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
72

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

  • - Sujetos que hayan recibido el PEI en el ensayo clínico 64.185-202
  • - Consentimiento informado escrito
  • Are the trial subjects under 18? yes
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) no
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • 未提供

研究者

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