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临床试验/DRKS00010928
DRKS00010928已完成不适用

Incidence and Resolution of Eribulin-induced peripheral Neuropathy (IRENE)

Eisai GmbH0 个研究点目标入组 341 人开始时间: 2016年8月19日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
Eisai GmbH
入组人数
341

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 Years 至 one(—)
性别
All

入选标准

  • Locally advanced or metastatic breast cancer with progression after at least one chemotherapeutic regimen for advanced disease eligible for treatment with eribulin according to Fachinformation. Prior therapy should have included an anthracycline and a taxane in either the adjuvant or metastatic setting unless patients were not suitable for these treatments. (Update Protocol V1.1 13Jun17)
  • - Maximum of two prior chemotherapeutic regimens for advanced disease.
  • - Age =18 years at the time of Informed Consent.
  • - Ability to understand and willingness to respond to questions related to their health.
  • - Decision for the patient to start treatment with eribulin has been made prior to inclusion in this study.
  • - Signed written Informed Consent.

排除标准

  • - Previous treatment with eribulin in any line of treatment.
  • - Contraindication according to the Fachinformation of eribulin.
  • - Pregnancy or lactation.
  • - Participation in an interventional clinical trial at the same time

研究者

发起方
Eisai GmbH

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