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临床试验/EUCTR2012-002298-69-PT
EUCTR2012-002298-69-PT进行中(未招募)不适用

A Multi-Center, Randomized, Double Blind, Placebo and Active-Controlled study with exploratory dose-ranging, to investigate the efficacy and safety of 16 weeks treatment with subcutaneous QGE031 in asthma patients not adequately controlled with high-dose inhaled corticosteroids and long acting ß2-agonists

ovartis Pharma Services AG0 个研究点目标入组 457 人开始时间: 2012年11月28日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
457

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

  • -A diagnosis of allergic asthma, uncontrolled on current medication
  • -History of at least 1 asthma exacerbation(s) during the last 1 year
  • - Forced Expiratory Volume in one second (FEV1) of = 40% and =80% of the predicted normal value;
  • - Reversibility following administration of bronchodilator must also be demonstrated (historical positive reversibility or bronchoprovocation result can be used)
  • Other inclusion criteria are listed in the clinical study protocol
  • 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 366
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 91

排除标准

  • -Baseline IgE levels or body weight outside the omalizumab dosing table
  • -Use of tobacco products within the previous 6 months
  • -Recent asthma attack/exacerbation or asthma worsening/respiratory infection
  • Other exclusion criteria are listed in the clinical study protocol.

研究者

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