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临床试验/JPRN-jRCT1080220402
JPRN-jRCT1080220402未知3 期

A Multicentre, Randomised, Open-Label, Parallel-Group, Phase III Post-Marketing Clinical Study to Compare the Overall Survival Between Gefitinib and Docetaxel in Patients With Advanced or Metastatic (Stage IIIB/IV), or Recurrent Non-Small Cell Lung Cancer, Who Have Failed One or Two Chemotherapy Regimens

AstraZeneca0 个研究点开始时间: 2007年6月12日最近更新:
适应症

试验速览

阶段
3 期
发起方
AstraZeneca

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
>= 20age old 至 ot applicable(—)
性别
All

入选标准

  • Ages Eligible for Study: 20 Years and above,
  • Genders Eligible for Study: Both
  • Inclusion Criteria:
  • - You are histologically or cytologically confirmed to have recurrent or metastatic NSCLC
  • - You have been treated with chemotherapy including platinums for NSCLC.

排除标准

  • - You have received treatment for non-small lung cancer within 4 weeks before your participation in this study (except for specific therapies)
  • - You have or had any disease of acute lung injury, idiopathic pulmonary fibrosis, pulmonary pneumonia, or pneumoconiosis evident on the X-ray
  • - You have or had any disease of radiation pneumonia or drug-induced pneumonia, which requires treatment with corticosteroids

研究者

发起方
AstraZeneca

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A Multicentre, Randomised, Open-Label,... | 临床试验