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
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