跳至主要内容
临床试验/jRCT2080220095
jRCT2080220095未知N/a

A confirmatory study of APTA-2217 in patients with chronic obstructive pulmonary disease (A placebo-controlled double-blind, parallel group study)

Mitsubishi Tanabe Pharma was the original trial sponsor; however Astra Zeneca is now the Responsible Party0 个研究点开始时间: 待定

试验速览

阶段
N/a
发起方
主要终点
-

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
干预模型
Double-blind, parallel-group comparative clinical study

入排标准

年龄范围
40age old over 至 No limit(—)
性别
All

入选标准

  • [Inclusion criteria]
  • Patients with chronic obstructive pulmonary disease who are 40 years old or more, current smoker or ex-smoker, 30 to 80 % of predicted FEV1 after inhalation of short acting beta stimulant.
  • [Exclusion criteria]
  • Patients with poorly controlled COPD, patients who need for long-term oxygen therapy, patients who have concurrent respiratory diseases such as asthma, diffuse panbronchiolitis, congenital sinobronchial syndrome, bronchiolitis obliterans, bronchiectasis, active tuberculosis, pneumoconiosis, pulmonary lymph vascular myaoma), which are considered to affect the evaluation.

排除标准

  • 未提供

结局指标

主要结局

-

Efficacy (pulmonary function test), safety and pharmacokinetics

次要结局

未报告次要终点

研究者

发起方
Mitsubishi Tanabe Pharma was the original trial sponsor; however Astra Zeneca is now the Responsible Party

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