跳至主要内容
临床试验/NL-OMON47707
NL-OMON47707招募中不适用

A phase I study to investigate the safety of TEG001 cell suspension for infusion in patients with relapsed/refractory Acute Myeloid Leukemia/high-risk Myelodysplastic Syndrome (IPSS-R score >4,5) relapsed/refractory or Multiple Myeloma - TEG001

niversitair Medisch Centrum Utrecht0 个研究点目标入组 18 人开始时间: 待定最近更新:

试验速览

阶段
不适用
状态
招募中
发起方
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
18 至 99(—)

入选标准

  • - Age >= 18-years
  • - Relapsed/refractory Acute Myeloid Leukemia/ high-risk Myelodysplastic
  • Syndrome (IPSS-R >4.5) or relapsed/refractory Multiple Myeloma, for which no
  • remaining standard of care or approved treatment options are available

排除标准

  • - In the investigators judgment, the subject is unlikely to complete all
  • protocol-required study visits or procedures
  • - Other concurrent malignancy requiring treatment
  • - Active endogenous retrovirus
  • - Active GVHD and/or systemic immune suppression for GVHD
  • - Uncontrolled infections
  • - Inadequate renal, hepatic, pulmonary and cardiac function
  • - Pregnant or lactating women

研究者

发起方
niversitair Medisch Centrum Utrecht

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