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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 人待定

概览

阶段
未知
干预措施
未指定
疾病 / 适应症
Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
发起方
Gachon University Gil Medical Center
入组人数
26
状态
尚未招募
最后更新
4年前

概览

简要总结

暂无简介。

注册库
who.int
开始日期
待定
结束日期
待定
最后更新
4年前
研究类型
Interventional Study
性别
All

研究者

入排标准

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.

结局指标

主要结局

未指定

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