跳至主要内容
临床试验/NCT01613053
NCT01613053No Longer Available不适用

Continuation of Drug Supply in Chinese Patients After CAMN107DBR01study Termination

Novartis Pharmaceuticals1 个研究点 分布在 1 个国家开始时间: 2012年6月6日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
No Longer Available
试验地点
1

研究概览

简要总结

Continuation of drug supply in Chinese patients after CAMN107DBR01study termination.

详细描述

Five patients who are on treatment of imatinib and deriving clinical benefit after CAMN107DBR01 study termination and written informed consent obtained will enter the trial, all five patients will receive Glivec (8oomg per day) treatment until tumor progression [by RECIST guidelines, version 1.0], unacceptable toxicity, death or withdrawal of consent.

研究设计

研究类型
Expanded Access

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

  • Five patients who are on treatment of imatinib and deriving clinical benefit after CAMN107DBR01 study termination and written informed consent obtained.

排除标准

  • 未提供

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验

Continuation of Drug Supply in Chinese Patients... | 临床试验