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临床试验/JPRN-UMIN000022494
JPRN-UMIN000022494已完成1 期

Investigator-Initiated Clinical Trials to assess the safety of SK-818 in patients with operable breast cancer - Investigator-Initiated Clinical Trials to assess the safety of SK-818 in patients with operable breast cancer

Kyushu University0 个研究点目标入组 18 人开始时间: 2016年6月1日最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
入组人数
18

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 70years-old(—)
性别
Female

入选标准

  • 未提供

排除标准

  • 1) Male 2) Multiple malignancies 3) Jaundice or cirrhosis 4) HBs antigen:positive (HBV testing for HBs antigen, HBs antibody and HBc antibody and HCV testing for HCV antibody should be performed within 3 months before operation) 5) Severe heart disease such as poorly controlled ischemic heart disease, heart failure and arrhythmia 6) Interstitial pneumonitis or pulmonary fibrosis 7) Blood disorders with disturbance of hematopoiesis such as Aplastic anemia or myelodysplastic syndromes 8) Active infection. 9) Severe drug allergy 10) Severe mental illness 11) Women during pregnancy or lactation and women who don't agree with contraception during the clinical trial 12) Participants in other clinical research within 30 days before giving informed consent 13) Patients as deemed appropriate for participation in this trial by medical doctors

研究者

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