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临床试验/JPRN-jRCT2080220373
JPRN-jRCT2080220373未知2 期

Phase II Study to Evaluate the Efficacy and Tolerability of Fulvestrant 250mg, 250mg (Plus 250mg Loading Regimen) and 500mg in Postmenopausal Women With ER +ve Advanced Breast Cancer Progressing or Relapsing After Previous Endocrine Therapy

AstraZeneca0 个研究点开始时间: 2007年4月10日最近更新:
适应症

试验速览

阶段
2 期
发起方
AstraZeneca

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

年龄范围
ot applicable 至 ot applicable(—)
性别
Female

入选标准

  • Genders Eligible for Study: Female
  • Inclusion Criteria:
  • - Breast Cancer has continued to grow after having received treatment with an anti-estrogen hormonal treatment such as tamoxifen or an aromatase inhibitor
  • - Requiring hormonal treatment
  • - Postmenopausal women defined as a woman who has stopped having menstrual periods

排除标准

  • - Treatment with more than one previous regimen of systemic anticancer therapy other than endocrine therapy for advanced breast cancer
  • - Treatment with more than one previous regimen of endocrine therapy for advanced breast cancer
  • - An existing serious disease, illness, or condition that will prevent participation or compliance with study procedures

研究者

发起方
AstraZeneca

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Phase II Study to Evaluate the Efficacy and... | 临床试验