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临床试验/KCT0008883
KCT0008883尚未招募Unknown

Post-transplant therapy with hypomethylating agent in Philadelphia chromosome negative adult acute lymphoblastic leukemia

Kyungpook National University Medical Center0 个研究点目标入组 33 人开始时间: 待定最近更新:
适应症

试验速览

阶段
Unknown
状态
尚未招募
入组人数
33

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
19(Year) 至 70(Year)(—)
性别
All

入选标准

  • 1) Patients who consented to the study
  • 2) Age > 19, <70
  • 3) Patients who diagnosed Philadelphila chromosome negative acute lymphoblastic leukemia and received standard chemotherapy
  • 4) Complete remission status after allogeneic stem cell transplantation
  • 5) Bone marrow blast < 5% after allogeneic stem cell transplantation & Patients who can receive decitabine (ANC > 1,000/uL & PLT > 50,000/uL)
  • 6) Patients less than 100 days after allogeneic stem cell transplantation
  • 7) Eastern Cooperative Oncology Group (ECOG) performance status 0-2
  • 8) Patients with appropriate liver, kidney, heart function
  • 9) A person who understands the contents of the clinical trial, is cooperative with the trial progress, and is judged to be able to participate until the end of the study

排除标准

  • 1) Pregnant or lactating women, or women who may become pregnant without adequate contraception
  • 2) Previous history of hypomethylation treatment
  • 3) Patients who have developed other malignant tumors within the past 5 years, excluding basal cell carcinoma of the skin, cervical carcinoma in situ, and papillary thyroid cancer that have been completely treated with the intention of cure
  • 4) Other serious illnesses or medical conditions
  • 5) Patients 100 days after allogeneic hematopoietic stem cell transplantation
  • 6) Men who want to become pregnant or donate sperm during a clinical trial
  • 7) Co-administration of other experimental drugs in clinical trials
  • 8) Any other person deemed unsuitable by the researcher.

研究者

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