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临床试验/NCT01291667
NCT01291667已完成不适用

A Phase III Randomized Study for HER2-Overexpressed Metastatic Breast Cancer Patients Treated by Trastuzumab( Cipterbin®) Plus vinorelbinE Simultaneously or Sequencely

Shanghai CP Guojian Pharmaceutical Co., Ltd.0 个研究点目标入组 330 人开始时间: 2009年5月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
330
主要终点
progress-free survival

研究概览

简要总结

Breast cancer is the most common malignant disease and the most frequent causes of cancer mortality in females worldwide. The situation is same as the world in China. Trastuzumab has been proved valuable treatment for HER2-positive breast cancer patients. Cipterbin® is developing by Shanghai CP Guojian Pharmaceutical Co.Ltd.Now we carried on the phase III trial in order to prove Cipterbin® 's efficacy and safety.

研究设计

研究类型
Observational
时间视角
Prospective

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • signed ICF
  • pathologic diagnosis breast cancer
  • HER2+ status defined as IHC3+ Staining or in situ hybridization positive at least 1 measurable lesion as per RECIST criteria age from 18y to 70y KPS>=70

排除标准

  • More than three prior chemotherapy lines for advanced disease LVEF<50%
  • prior exposure vinorebine for breast cancer
  • prior exposure Trastuzumab for breast cancer
  • uncontrolled brain metastasis
  • breastfeeding or pregnant

结局指标

主要结局

progress-free survival

次要结局

  • overall response rate,safety

研究者

发起方
Shanghai CP Guojian Pharmaceutical Co., Ltd.
申办方类型
Industry

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