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临床试验/EUCTR2013-005614-35-BE
EUCTR2013-005614-35-BE进行中(未招募)1 期

A 52-Week, Multicentre, Randomized, Double-Blind, Parallel Group, Placebo Controlled, Phase 3 Study to Evaluate the Efficacy and Safety of Tralokinumab in Adults and Adolescents with Asthma Inadequately Controlled on Inhaled Corticosteroid Plus Long-Acting ß2-Agonist

AstraZeneca AB0 个研究点目标入组 1,140 人开始时间: 2014年10月24日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
1,140

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. Age 12 -75
  • 2. Documented physician-diagnosed asthma.
  • 3. Documented treatment with ICS at a total daily dose corresponding to =500µg fluticasone propionate dry powder formulation equivalents) and a LABA
  • 4. Morning pre-BD FEV1 value of =40 and <80% value (<90% for patients 12 to 17 years of age) of their PNV.
  • 5. Post-BD reversibility of =12% and =200 mL in FEV1
  • 6. ACQ-6 score =1.5
  • Are the trial subjects under 18? yes
  • Number of subjects for this age range: 100
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 960
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 60

排除标准

  • 1. Pulmonary disease other than asthma
  • 2. History of anaphylaxis following any biologic therapy
  • 3. Hepatitis B, C or HIV
  • 4. Pregnant or breastfeeding
  • 5. History of cancer
  • 6. Current tobacco smoking or a history of tobacco smoking for = 10 pack-years
  • 7. Previous receipt of tralokinumab

研究者

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