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临床试验/EUCTR2006-001907-13-ES
EUCTR2006-001907-13-ES进行中(未招募)1 期

etrozol frente a Letrozol más Lapatinib (GW572016) en cáncer de mama hormosensible y operable, con HER-2 negativo. Estudio en Fase II aleatorizado y doble ciego con evaluación de biomarcadores. (Letrozole versus Letrozole plus lapatinib (GW572016) in hormone-sensitive, HER-2 negative operable breast cancer. A double blind randomized phase II study with biomarker evaluation) - LETLOB

GlaxoSmithKline Research and Development Limited0 个研究点目标入组 0 人开始时间: 2007年7月2日最近更新:
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试验速览

阶段
1 期
状态
进行中(未招募)
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
Female

入选标准

  • Histologically confirmed infiltrating primary breast cancer of > 2.0 cm in size in largest clinical diameter; ER and/or PgR positive cancer (> 10% of positive cancer cell assessed by IHC); postmenopausal status; HER2 negative tumors (IHC 0-2+, or FISH negative); availability of tumor tissue suitable for biological and molecular examination before starting primary treatment; age over 18; ECOG PS 0-1; normal organ and marrow function; cardiac ejection fraction within the institutional range of normal as measured by echocardiogram or MUGA scan; ability to understand and the willingness to sign a written informed consent document; ability to swallow and retain oral medication.
  • 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
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Stage IIIB, IIIC and inflammatory breast cancer; Stage IV breast cancer; contraindication to the treament with letrozole; prior treatment with chemotherapy, endocrine therapy and radiotherapy. Prior treatment with EGF targeting therapies; Treatment with any other investigational agents, or with all herbal (alternative) medicines; history of allergic reactions attributed to compounds of similar chemical or biological composition to lapatinib; uncontrolled inter-current illnesses; HIV-positive patients receiving combination anti-retroviral therapy; GI tract disease resulting in the inability to take oral medication; concomitant requirement for medication classified as CYP3A4 inducers or inhibitors

研究者

发起方
GlaxoSmithKline Research and Development Limited

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