跳至主要内容
临床试验/NCT00264134
NCT00264134终止1 期

A Phase I/II Trial: Docetaxel, Irinotecan, and Carboplatin in the Treatment of Extensive Stage Small Cell Lung Carcinoma

Kentuckiana Cancer Institute2 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2003年6月1日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
终止
发起方
入组人数
40
试验地点
2
主要终点
Primary Objective: To determine the maximum tolerated dose of docetaxel when given with Irinotecan and Carboplatin for the treatment of inoperable lung cancer.

研究概览

简要总结

Primary Objective: To determine the maximum tolerated dose of docetaxel when given with Irinotecan and Carboplatin for the treatment of inoperable lung cancer.

Secondary Objective: To evaluate the dose-related toxicities of this triple regimen in patients with inoperable lung cancer.

详细描述

A phase I/II dose escalating study to determine the maximum tolerated dose of docetaxel when given with Irinotecan and Carboplatin for the treatment of inoperable lung cancer.

研究设计

研究类型
Interventional
分配方式
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

  • 18 years or older unresectable lung cancer measurable or evaluable lesions Karnofsky PS greater than or equal to 60%

排除标准

  • untreated CNS metastases

结局指标

主要结局

Primary Objective: To determine the maximum tolerated dose of docetaxel when given with Irinotecan and Carboplatin for the treatment of inoperable lung cancer.

次要结局

  • Secondary Objective: To evaluate the dose-related toxicities of this triple regimen in patients with inoperable lung cancer.

研究者

发起方
Kentuckiana Cancer Institute
申办方类型
Other

研究点 (2)

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