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临床试验/KCT0006222
KCT0006222尚未招募未知

Intensity-adjusted SAlvage chemotheraPy Plus FLT3-inHibitor Gilteritinib In RElapsed/refractory acute myeloid leukemia with mutated FLT3-ITD/TKD

Gachon University Gil Medical Center0 个研究点目标入组 26 人开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
尚未招募
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 Study

入排标准

年龄范围
19?(Year) 至 o Limit(—)
性别
All

入选标准

  • Relapsed or refractory mutated FLT3-ITD/TKD AML
  • No prior exposure to Gilteritinib (prior exposure of other FLT3-inhibitors is permitted including quizartinib or midostaurin)
  • Mean QTcF interval of ECG readings is 480 ms or shorter
  • Written informed consent must be given.
  • Patients must be 19 years of age or older.

排除标准

  • prior exposure to gilteritinib
  • Patients who are not able to receive FLAG-Ida or LoDAC
  • Acute promyelocytic leukemia with t(15;17) or PML/RARa rearrangement
  • Patients with CNS involvement of leukemic blasts will not be excluded.
  • Patients with extramedullary relapse(s) only will be excluded.
  • Uncontrolled active infection
  • Uncontrolled bleeding
  • Patients who are pregnant or lactating.
  • Patients having a psychiatric disorder or mental deficiency severe as to make compliance with the treatment unlike, and making informed consent impossible.

研究者

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