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临床试验/NCT00298688
NCT00298688已完成2 期

Phase II Study of Iressa in Relapsed and Refractory Small Cell Lung Cancer

AstraZeneca3 个研究点 分布在 2 个国家目标入组 56 人开始时间: 2004年9月最近更新:
适应症
相关药物

试验速览

阶段
2 期
状态
已完成
发起方
AstraZeneca
入组人数
56
试验地点
3
主要终点
To determine the disease control rate in these patients

研究概览

简要总结

The purpose of this study is to determine the disease control rate at trial closure and after the first stage of the study in patients with relapsed or refractory SCLC and measurable disease treated with gefitinib

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Provision of written informed consent
  • Histologically confirmed, relapsed or refractory SCLCr
  • Aged 18 or over and a life expectancy of more than 2 months

排除标准

  • Any evidence of clinically active interstitial lung disease
  • Other co-existing malignancies or malignancies diagnosed within the last 5 years, with the exception of basal cell carcinoma or cervical cancer in situ.

结局指标

主要结局

To determine the disease control rate in these patients

次要结局

  • To determine the objective response rate at trail closure in these patients
  • To determine the time to progression-or-death in these patients
  • To determine overall survival in these patients

研究者

发起方
AstraZeneca
申办方类型
Industry

研究点 (3)

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