JPRN-UMIN000009582已完成2 期
Weekly paclitaxel in combination with bevacizumab in patient with HER2 nagative breast cancer who were previously treated with taxane - PhaseII - - SBP-05: CARP trial Clinical evaluation of avastin to patients relapsed after taxane
Setouchi Breast Project Comprehensive Support Organization0 个研究点目标入组 33 人开始时间: 2012年12月19日最近更新:
适应症
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 33
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 ot applicable(—)
- 性别
- Female
入选标准
- 未提供
排除标准
- •1) Prior therapy with bevacizumab 2) Hypersensitivity to paclitaxel or drugs using the vehicle Cremophor, Chinese hamster ovary cell derived products or other recombinant humanized antibodies 3) Symptomatic brain metastasis 4) Women who is pregnant, lactating or declined contraception 5) Patients with a non-healing wound or fracture 6) Uncontrolled hypertension (SBP>150 mmHg, DBP>100 mmHg) 7) Patients receiving anticoagulant therapy within 10 days prior to registration (aspirin <=325 mg/day is allowed.), or patients need anticoagulant therapy during study 8) Symptomatic congestive heart failure, unstable angina, uncontrolled arrhythmia, myocardial infarction within 12 months prior to study entry 9) Idiopathic pulmonary fibrosis, interstitial lung disease 10) Baseline left ventricular ejection fraction (LVEF) > 50% measured by echocardiography 11) Current or previous history (within 12 months) of symptomatic cerebrovascular disease 12) Current or previous history (within 12 months) of deep vein thrombosis or pulmonary embolism 13) Current or previous history (within 12 months) of GI perforation 14) Synchronous or metachronous tumors with <5 years disease-free period 15) Patients ineligible to the study based on decision of attending physician or site principal investigators
研究者
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