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临床试验/NCT00241462
NCT00241462终止不适用

Faslodex Observations During Regular Use by Advanced Mammacarcinoma Patients

AstraZeneca1 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2005年6月最近更新:
适应症

试验速览

阶段
不适用
状态
终止
发起方
AstraZeneca
入组人数
150
试验地点
1

研究概览

简要总结

The purpose of this study is to identify which patients, receiving Faslodex within the approved label, benefit most from Faslodex treatment.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Prospective

入排标准

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

入选标准

  • Postmenopausal
  • Locally advanced or metastatic hormone sensitive breast cancer with known estrogen receptor (ER) and progesterone receptor (PR) status
  • Patient had a recurrence during or after adjuvant anti-oestrogen treatment or progression of the disease during anti-oestrogen treatment

排除标准

  • Life threatening metastases

研究者

发起方
AstraZeneca
申办方类型
Industry

研究点 (1)

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