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临床试验/JPRN-UMIN000004084
JPRN-UMIN000004084已完成未知

Phase1 trial of weekly paclitaxel and gemcitabine in previously anthracycline-treated patients with locally advanced or metastatic breast cancer (SBCCSG-17) - Phase1 trial of weekly paclitaxel and gemcitabine

Saitama Breast Cancer Clinical Study Group(SBCCSG)0 个研究点目标入组 12 人开始时间: 2010年8月22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
12

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

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)Patient had received gemcitabine treatment in the past. 2)Patient with inflammatory carcinoma. 3)Patient apparently or possibly has pulmonary fibrosis or pneumonia. 4)Patient is class III or IV of NYHA functional classification or patient has cardiac infarction occurred within past six months. 5)Patient has body cavity fluid which needs to be treated. 6)Patient has active infection. 7)Patient has serious coexisting illness (including diabetes which is difficult to control). 8)Patient has serious drug allergy. 9)Patient has serious psychiatric illness that can make his/her decisions unstable or uncertain. 10)Patient had had bone marrow transplantation or stem cell transplantation. 11)Patient has symptomatic brain metastasis. 12)Patient receives continuous whole-body administration of steroid drugs (orally or intravenously.) 13)Patient has active double cancer. 14)Patient is apparently/possibly during pregnancy, lactation expectant, or desiring future fertility in the period from informed consent day to 3 months after final test drug administration. 15)Patient has received unapproved drugs or other investigational drugs within 30 days before the registration date. 16)Patient is judged unsuitable as object of this clinical trial by the principal investigator or the physician in charge.

研究者

发起方
Saitama Breast Cancer Clinical Study Group(SBCCSG)

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