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临床试验/JPRN-UMIN000007121
JPRN-UMIN000007121已完成未知

Evaluation of safety and efficacy of eribulin for patients advanced or recurrent HER2 negative breast cancer who have been treated with anthracyclines and taxanes - KBC-SG1105

Kyushu Breast Cancer Study Group0 个研究点目标入组 50 人开始时间: 2012年1月24日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
50

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
20years-old 至 75years-old(—)
性别
Female

入选标准

  • 未提供

排除标准

  • 1 ineligible patients complicated with infectious diseases or who suspected infectious diseases with fever 2. diarrheal , ileus 3. GI bleeding 4.severe drug allergy 5. severe renal and/ or liver dysfunction 6.significant interstitial pneumonia or pulmonary fibrosis by chest radiograph 7.pleural effusion, peritoneal effusion 8.poorly controlled hypertension or diabetes mellitus 9.maintenance therapy with systemic corticosteroids 10.pregnant women or women with suspected pregnancy 11.patients who received blood transfusion, blood products or G-CSF within 7 days prior to this study 12.presence of the active other malignancies 13.severe psychiatric disorder 14 brain metastases 15.patients judged by the investigator to be unfit for the study

研究者

发起方
Kyushu Breast Cancer Study Group

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