跳至主要内容
临床试验/EUCTR2013-001089-40-BG
EUCTR2013-001089-40-BG进行中(未招募)1 期

An extension study to evaluate the sustainability of clinical benefits, safety and tolerability of secukinumab in patients with active Ankylosing Spondylitis

ovartis Pharma Services AG0 个研究点目标入组 274 人开始时间: 2013年11月21日最近更新:
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
274

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

  • - Patients having completed the core study CAIN457F2305.
  • - Indication for treatment extension
  • Other protocol-defined inclusion criteria may apply.
  • 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 261
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 13

排除标准

  • - History of hypersensitivity to secukinumab or to any drug of similar chemical classes.
  • - Use of any investigational drug other than secukinumab during the core study CAIN457F2305.
  • Other protocol-defined exclusion criteria may apply.

研究者

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