跳至主要内容
临床试验/NCT00878930
NCT00878930已完成不适用

Non-interventional Report on Parameters of Acceptability, Efficacy and Compliance of Fulvestrant in Post-menopausal Patients With Advanced Breast Cancer HR Positive Who Progresses to One Prior Endocrine Therapy With Antiestrogens

AstraZeneca1 个研究点 分布在 1 个国家目标入组 500 人开始时间: 2009年4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
AstraZeneca
入组人数
500
试验地点
1
主要终点
To collect real life data of acceptability and compliance on the use of Faslodex in the Argentine population.

研究概览

简要总结

The objectives of this study is to obtain information of Faslodex use in the treatment of breast cancer in the clinical practice in Argentina.

详细描述

In Argentina, Faslodex is indicated for treating postmenopausal women with hormone receptor-positive locally advanced or metastatic breast cancer with recurrence during or after adjuvant anti-oestrogen therapy or disease progression during anti-oestrogen treatment. This study will provide information regarding the acceptability and compliance of Argentina patients to Faslodex and will provide information regarding the efficacy of this treatment in local population.

研究设计

研究类型
Observational
观察模型
Cohort
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 women with hormone receptor-positive locally advanced or metastatic breast cancer with recurrence during or after adjuvant anti-estrogen therapy or disease progression during anti-estrogen treatment, currently receiving Faslodex
  • Signature of the informed consent

排除标准

  • Any contraindication to Faslodex administration

结局指标

主要结局

To collect real life data of acceptability and compliance on the use of Faslodex in the Argentine population.

时间窗: monthly

To collect real life data of efficacy on the use of Faslodex in the Argentine population.

时间窗: monthly

次要结局

未报告次要终点

研究者

发起方
AstraZeneca
申办方类型
Industry

研究点 (1)

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