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临床试验/EUCTR2011-000198-29-GB
EUCTR2011-000198-29-GB
进行中(未招募)
不适用

A Phase 1b/2 Randomized Study of MEDI-573 in Combination with an Aromatase Inhibitor (AI) Versus AI Alone in Women with Metastatic Breast Cancer (MBC)

MedImmune, LLC0 个研究点目标入组 178 人2011年8月12日

概览

阶段
不适用
干预措施
未指定
疾病 / 适应症
未指定
发起方
MedImmune, LLC
入组人数
178
状态
进行中(未招募)
最后更新
13年前

概览

简要总结

暂无简介。

注册库
who.int
开始日期
2011年8月12日
结束日期
待定
最后更新
13年前
研究类型
Interventional clinical trial of medicinal product
性别
Female

研究者

入排标准

入选标准

  • Histologically\-confirmed MBC not deemed amenable to curative surgery or curative radiation therapy
  • Tumors are positive for ER, PgR, or both
  • Tumors must be negative for HER2 (by FISH or CISH)
  • Female gender and age \= 18 years at time of study entry Postmenopausal
  • Karnofsky Performance Status \= 70
  • Life expectancy of \= 6 months
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1\.2 Adults (18\-64 years) yes
  • F.1\.2\.1 Number of subjects for this age range 160

排除标准

  • Subjects who received prior chemotherapy, hormonal therapy, immunotherapy or biologic therapy for advanced or metastatic disease with the following exceptions:
  • Prior adjuvant therapy with an AI or tamoxifen is allowed, provided treatment ended at least 2 weeks prior to the first dose of MEDI\-573
  • Prior neoadjuvant and/or adjuvant chemotherapy for breast cancer is allowed
  • Extensive symptomatic visceral disease including hepatic involvement and pulmonary lymphangitic spread of tumor, or disease that is considered by the investigator to be rapidly progressing or life threatening (eg, subjects who are intended for chemotherapy)
  • Active brain metastases with the exception of subject has been treated and are asymptomatic and there has been no evidence of CNS progression for at least 4 weeks of first dose of MEDI\-573 Evidence of ongoing spinal cord compression or leptomeningeal carcinomatosis
  • Unresolved toxicities from prior therapy with the exception of alopecia that have not resolved to \= Grade 1 at the time of starting study treatment
  • Previous treatment with agents that target the IGF receptor History of allergy or reaction attributed to compounds of chemical or biologic composition similar to those of MEDI\-573 or AI
  • History of another invasive malignancy within 5 years except for curatively resected nonmelanoma skin cancer or carcinoma in situ of the cervix
  • Poorly controlled diabetes mellitus

结局指标

主要结局

未指定

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