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临床试验/EUCTR2014-002195-90-GB
EUCTR2014-002195-90-GB进行中(未招募)1 期

Adults with acute myeloid leukaemia or high-risk myelodysplastic syndrome (AML19) - AML19

Cardiff University0 个研究点目标入组 250 人开始时间: 2015年6月10日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
250

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • They have one of the forms of CD33 positive (any level) favourable, standard risk or unknown cytogenetics, de novo AML as defined by the WHO Classification
  • WHO performance status 0-2.
  • They are considered suitable for intensive chemotherapy.
  • Age 16 to 60 years of age, with the following caveats: o Patients over 60 are eligible if intensive therapy is considered a suitable option o Patients must be =18 to be eligible to receive Midostaurin
  • A negative pregnancy test within 2 weeks prior to trial entry in WOCBP to be repeated throughout the trial prior to each course of protocol treatment.
  • Sexually mature males and females must agree to use an adequate and medically accepted method of contraception throughout the study and for 6 months following treatment (unless patient is female and received Mylotarg- in which case it should be 7 months) if they or their sexual partners are women of childbearing potential (WOCBP).
  • Written informed consent. · Patients must have Serum Alanine Aminotransferase (ALT) and Aspartate Aminotransferase (AST) =2.5 ×ULN and bilirubin =2×ULN · For Midostaurin: Patients must have a FLT3 TKD or ITD mutation detected by the central laboratory in Cardiff
  • Are the trial subjects under 18? yes
  • Number of subjects for this age range: 0
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 240
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range 0

排除标准

  • Patients with APL, secondary AML, therapy-related AML, high risk myelodysplastic syndrome with <20% bone marrow blasts, or de novo AML with known adverse risk cytogenetics.
  • Concurrent active malignancy requiring treatment.
  • Patients who are pregnant or lactating.
  • Known infection with Human Immunodeficiency Virus (HIV).
  • Previous cytotoxic chemotherapy for AML. Note: Hydroxycarbamide, or similar low-dose therapy, to control the white count prior to initiation of intensive therapy is not an exclusion
  • Blast transformation of chronic myeloid leukaemia (CML).
  • The physician and patient consider that intensive therapy is not an appropriate treatment option.

研究者

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