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临床试验/EUCTR2006-001834-42-IT
EUCTR2006-001834-42-IT进行中(未招募)不适用

A Multi-Center, Open label, Repeated Dose Range Finding Study to Evaluate the Safety, Tolerability, Immunogenicity, Pharmacokinetics and Efficacy of an Anti-IL-1 946; Monoclonal Antibody ACZ885 Given Subcutaneously in Pediatric Subjects with Active Systemic Juvenile Idiopathic Arthritis SJIA - CACZ885A2203

OVARTIS PHARMA AG0 个研究点开始时间: 2007年1月9日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)

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

  • male female subjects aged 4 to 20 having passed screening exams female child bearing potential with negative pregnancy test at screening and willing to use contraception for three months afetr the end of treatment
  • 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

  • use of etanercept in the four weeks prior to the baseline visit adalimumab in the eight weeks prior to the baseline visit infliximab in the 8 w prior to baseline visit

研究者

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