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临床试验/JPRN-UMIN000018730
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Haploidentical transplantation with post-transplant cyclophosphamide - Haploidentical Transplantation (Kurume University PT-CY1)

Division of Hematology & Oncology, Department of Medicine, Kurume University School of Medicine0 个研究点目标入组 21 人开始时间: 2015年9月1日最近更新:

试验速览

阶段
未知
状态
已完成
发起方
入组人数
21

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
15years-old 至 70years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1. Patients who are positive for HBs antigen, HCV antibody, or HIV antibody. 2. Patients with active other malignancies. 3. Patients with active infectious disease. 4. Women who are pregnant, of childbearing potential, or lactating. 5. Patients who experienced serious hypersensitivity or anaphylaxis to cyclophosphamide, fludarabine, tacrolimus, mycophenolate mofetil. 6. Positive anti-donor HLA antibody. 7. Patients who need chemotherapy within 13 days before transplantation. 8. Patients who are not eligible for this study at the discretion of the investigator.

研究者

发起方
Division of Hematology & Oncology, Department of Medicine, Kurume University School of Medicine

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