跳至主要内容
临床试验/EUCTR2007-003627-20-GB
EUCTR2007-003627-20-GB进行中(未招募)1 期

Comparative Relative Lung Bioavailability of HFA-Seretide via spacer devices in healthy volunteers - Lung Bioavailability of HFA-Seretide via spacers

niversity of Dundee, Research & Innovation Services0 个研究点目标入组 20 人开始时间: 2008年12月16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)
发起方
入组人数
20

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

  • 1.Healthy Volunteers
  • 2.Male or female 18-65
  • 3.Informed Consent
  • 4.Ability to comply with the requirements of the 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
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • 1.No respiratory disease
  • 3.Recent respiratory tract infection (2 months).
  • 4.Any other clinically significant medical condition such as unstable angina, acute myocardial infarction in the preceding 3 months, recent TIA/ CVA,that may endanger the health or safety of the participant, or jeopardise the protocol.
  • 5.Any significant abnormal laboratory result as deemed by the investigators
  • 6.Pregnancy, planned pregnancy or lactation
  • 7.Known or suspected contra-indication to any of the IMP’s
  • 8.Concomitant use of medicines (prescribed, over the counter or herbal) that may interfere with the trial

研究者

发起方
niversity of Dundee, Research & Innovation Services

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