跳至主要内容
临床试验/PER-010-10
PER-010-10未知未知

AN OPEN-LABEL RANDOMIZED, PARALLEL, TWO-ARM PHASE II STUDY COMPARING BMS-690514 + LETROZOLE WITH LAPATINIB + LETROZOLE IN RECURRENT AND METASTATIC BREAST CANCER PATIENTS WHO ARE HORMONE RECEPTOR POSITIVE DESPITE HER2 STATUS AND WHO RELAPSED WHILE RECEIVING OR AFTER COMPLETING ADJUVANT ANTIENDOCRINE THERAPY

BRISTOL MYERS SQUIBB COMPANY,0 个研究点目标入组 0 人开始时间: 2010年5月21日最近更新:

试验速览

阶段
未知

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
18 至 100(—)
性别
Female

入选标准

  • 1) Informed written consent approved by the IRB / IEC voluntarily signed and dated form in accordance with the guidelines.
  • 2) Invasive breast cancer documented histologically positive for ER + and / or PgR + in 10% of tumor cells or more, with tumor tissue from previous surgery available for analysis of ER / PR, EGFR, PTEN and PIK3CA.
  • 3) Patients must have previously received adjuvant therapy for breast cancer with tamoxifen or exemestane anastraozol. the sequential use of antihormonal agents are allowed.
  • 4) Patients receiving cytotoxic chemotherapy (adjuvant setting in metastatic, or neoadjuvant) therapy must have completed at least 4 weeks before the first dose of randomized study medication.

排除标准

  • 1) Patients who have received prior hormonal therapy for metastatic disease.
  • 2) Patients who have received prior hormonal therapy for metastatic disease.
  • 3) Symptomatic patients with brain metastases.
  • 4) Patients with signs or symptoms suggestive of understanding

研究者

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