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临床试验/JPRN-UMIN000007281
JPRN-UMIN000007281招募中未知

Safety and efficacy of reduced intensity myeloablative conditioning regimen with fludarabine, cytarabine arabinoside, and cyclophosphamide for hematological malignancies - GHSG-SCT1101

Gifu University Hospital0 个研究点目标入组 36 人开始时间: 2012年2月13日最近更新:
适应症

试验速览

阶段
未知
状态
招募中
发起方
入组人数
36

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
All

入选标准

  • 未提供

排除标准

  • 1) Patients with HIV 2) Patients who received gemtuzumab ozogamicin within 3 months 3) Patients with another active malignancy 4) Patients with severe mental disease 5) Patients with severe central nervous system (CNS) lesions (except for CNS lesions of the underlying disease) 6) Patients with active infection 7) Patients who have history of chemotherapy within 21 days before transplantation (except hydroxyurea, cytarabine, or etoposide therapy for blast control) 8) Patients who have hypersensitivity to drugs included in this protocol 9) Patients who are judged inappropriate for the entry into the study by the principle doctor.

研究者

发起方
Gifu University Hospital

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