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临床试验/NL-OMON44473
NL-OMON44473已完成4 期

Therapeutic drug monitoring of asparaginase and methotrexate metabolism in childhood acute lymphoblastic leukemia. - Asparaginase and methotrexate in childhood acute lymphoblastic leukemia.

Erasmus MC, Universitair Medisch Centrum Rotterdam0 个研究点目标入组 70 人开始时间: 待定最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
入组人数
70

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
2 至 99(—)

入选标准

  • - Patients who are treated according to the DCOG ALL11 protocol.
  • - Informed consent have to be signed by parents/guardians and patient of 12 years or older.

排除标准

  • - Patients who have a contraindication for asparaginase.
  • - Patients with hypersensitivity reactions to PEGasparaginase will switch to Erwinia asparaginase. These patients will be included in the population pharmacokinetic analysis up to the point a hypersensitivity reaction occurs. They will still remain included in the 3 other studies.
  • - Patients who are stratified as high risk will be excluded from the methotrexate study.

研究者

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