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临床试验/NCT00238849
NCT00238849Unknown2 期

Phase II Study of Oxaliplatin in Combination With Navelbine for the Second-Line Treatment of Advanced and Metastatic Non-Small Cell Lung Cancer

Integrated Community Oncology Network3 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2005年10月14日最近更新:
适应症
相关药物

试验速览

阶段
2 期
发起方
入组人数
40
试验地点
3
主要终点
Efficacy

研究概览

简要总结

The purpose of this study is to determine the response rate to treatment with oxaliplatin and Navelbine in patients with previously treated NSCLC. Oxaliplatin and Navelbine have not been clinically evaluated yet. However, Navelbine has been safely administered with other platinum compounds.

详细描述

This is a non-randomized trial for patients with previously treated Non-small cell lung cancer. Each patient will receive 6 cycles of chemotherapy consisting of Oxaliplatin and Navelbine. Oxaliplatin is given intravenously every 21 days and Navelbine is administered Intravenously on day 1 and day 8 every 21 days.

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

  • Locally advanced or metastatic non-small cell lung cancer that has recurred, progressed, or failed to respond to previous systemic chemo.
  • Measurable disease
  • Good performance status (ECOG 0,1 or 2)

排除标准

  • Previously treated with Oxaliplatin or Navelbine
  • Symptomatic CNS metastases

结局指标

主要结局

Efficacy

次要结局

  • Time to progression
  • Duration of response
  • Survival
  • Toxicity profile

研究者

发起方
Integrated Community Oncology Network
申办方类型
Other

研究点 (3)

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Phase II Study of Oxaliplatin and Navelbine for... | 临床试验