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临床试验/CTRI/2009/091/000607
CTRI/2009/091/000607已完成3 期

A phase III trial of vinflunine plus capecitabine versus capecitabine alone in patients with advanced breast cancer previously treated with or resistant to an anthracycline and who are taxane resistant - L00070 IN 305 B0

Institut de Recherche Pierre Fabre0 个研究点目标入组 764 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
已完成
入组人数
764

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • 1. Patients must give written informed consent
  • 2. Women with confirmed carcinoma of the breast.
  • 3. Patients must have received a minimum cumulative dose of anthracycline or be resistant to an anthracycline
  • 4. Patients must be resistant to taxane therapy

排除标准

  • 1.Patients having received > 3 regimens of chemotherapy
  • 2.Prior therapy with capecitabine and/or vinca alkaloids (including vinflunine).

研究者

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