跳至主要内容
临床试验/EUCTR2007-002133-36-IT
EUCTR2007-002133-36-IT进行中(未招募)不适用

A multicenter, randomised, double-blind clinical study to examine the efficacy and safety of ZARZENDA in comparison to Elidel in the management of mild to moderate Atopic Dermatitis in children and adolescents. - ND

INTENDIS GMBH0 个研究点目标入组 60 人开始时间: 2009年1月27日最近更新:
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
INTENDIS GMBH
入组人数
60

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

  • ICf signed by legal resp and assent oof subject mild to moderate AD (IGA 3 or 4) AD history for at least one year 2-17 years of age at baseline
  • 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

  • Pregnancy, breast feeding Indication for systemic therapy of AD Sinsitivity to Zarzenda or to Butyrospermum Parkii

研究者

发起方
INTENDIS GMBH

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