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临床试验/JPRN-jRCT2080221070
JPRN-jRCT2080221070未知3 期

An Open Label, Randomised, Parallel Group, Multicentre Study to Compare ZOLADEX 10.8 mg Given Every 12 Weeks With ZOLADEX 3.6 mg Given Every 4 Weeks in Pre-menopausal Women With Oestrogen Receptor Positive Advanced Breast Cancer

AstraZeneca0 个研究点开始时间: 2010年4月14日最近更新:
适应症

试验速览

阶段
3 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
>= 20age old 至 ot applicable(—)
性别
Female

入选标准

  • Female 20 years or older and pre-menopausal.
  • Pre-menopausal defined as
  • 1) last menses within 1 year of randomisation, and
  • 2) E2 10 pg/mL or more, and FSH 30 mIU/mL or less within 4 weeks of randomisation.
  • For patients who have had a hysterectomy, it is acceptable to meet only 2)
  • - Hormone sensitivity (ER positive) of primary or secondary tumour tissue.
  • - Histological/cytological confirmation of breast cancer and are candidates to receive hormonal therapy as therapy for advanced breast cancer.

排除标准

  • - Patients who have received tamoxifen or other hormonal therapies as adjuvant therapy for breast cancer within 24 weeks before randomisation and/or who have received prior treatment with hormonal therapies for advanced breast cancer
  • - Patients who have received LHRHa as adjuvant therapy for breast cancer within 48 weeks before randomisation
  • - Patients who have relapsed during adjuvant hormonal therapy or within 48 weeks after completion of adjuvant hormonal therapy and/or patients who have relapsed during adjuvant chemotherapy or within 24 weeks after completion of adjuvant chemotherapy.

研究者

发起方
AstraZeneca

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