跳至主要内容
临床试验/JPRN-jRCT2080221337
JPRN-jRCT2080221337终止1 期

A Phase I/II Study of WT4869 in Patients with Myelodysplastic Syndromes (MDS)

Sumitomo Dainippon Pharma Co., Ltd.0 个研究点目标入组 26 人开始时间: 2010年12月22日最近更新:
适应症

试验速览

阶段
1 期
状态
终止
入组人数
26

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
>= 18age old 至 ot applicable(—)
性别
All

入选标准

  • Phase I: histologically and/or cytologically confirmed WHO-defined MDS
  • - Phase II: histologically and/or cytologically confirmed MDS (WHO-defined) or refractory anemia with excess blasts in transformation (RAEB-t, FAB-defined)
  • - 18 years or older
  • - Eastern Cooperative Oncology Group (ECOG) performance status of 0-2
  • - HLA-A*2402

排除标准

  • - Patients with concomitant infectious disease that requiring systemic antibiotics, systemic antiviral drugs or other treatment
  • - Pregnant or lactating females
  • - Anti-HIV antibody, HBs antigen or anti-HCV antibody positivity in the last 3 months prior to enrollment

研究者

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