跳至主要内容
临床试验/EUCTR2017-001678-40-Outside-EU/EEA
EUCTR2017-001678-40-Outside-EU/EEA进行中(未招募)1 期

An extension study of safety of canakinumab in Japanese patients with periodic fever syndromes

ovartis pharma AG0 个研究点目标入组 4 人开始时间: 2017年5月15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
4

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

  • Key Completed Epoch 4 of the CACZ885N2301 study in Japan before the approval of canakinumab in Japan. Written informed consent. Parent or legal guardian's written informed consent and child's assent, if appropriate, are required before any assessment is performed for patients < 20 years of age
  • Are the trial subjects under 18? yes
  • Number of subjects for this age range: 1
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 3
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Key Any conditions or significant medical problems in which the investigator judges the patient should not enter this extension study

研究者

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