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临床试验/EUCTR2008-006161-84-GB
EUCTR2008-006161-84-GB进行中(未招募)不适用

ARTiST - Aromasin Randomised Trial +/- Sutent as neoadjuvant Therapy for post-menopausal women with breast cancer. - ARTiST

Cambridge University Hospitals NHS Foundation Trust0 个研究点目标入组 100 人开始时间: 2009年4月16日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
100

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

  • Key Inclusion criteria
  • -Ultrasound Size: greater than 1 cm.
  • -Diagnosis of invasive breast cancer on core biopsy.
  • -Patients with localised or locally advanced invasive breast cancer.
  • -Histological grade : G1-3.
  • -ER positive (Allred = 4).
  • 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

  • - Previous history of cancer, excluding basal cell carcinoma or cervical carcinoma in-situ.
  • - Previous deep vein thrombosis or pulmonary embolism.
  • - Uncontrolled hypertension.
  • -Any of the following within the 12 months prior to study drug administration: myocardial infarction, severe/unstable angina, coronary/peripheral artery bypass graft, symptomatic congestive heart failure, cerebrovascular accident or transient ischemic attack.
  • -Pre-existing thyroid abnormality with thyroid function that cannot be maintained in the normal range with medication.
  • -Ongoing cardiac dysrhythmias of = grade 2 (NCI CTCAE grading version 3.0), atrial fibrillation of any grade, or prolongation of the QTc interval >470 msec.
  • -Treatment with terfenadine, quinidine, procainamide, disopyramide, sotalol, probucol, bepridil, haloperidol, risperidone, ketoconazole or indapamide
  • - Known human immunodeficiency virus (HIV) positive, or acquired immunodeficiency syndrome (AIDS) related illness.
  • - Osteoporosis

研究者

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