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临床试验/JPRN-jRCT2031220084
JPRN-jRCT2031220084进行中(未招募)3 期

Phase 3, randomized, double-blind study of the efficacy of TM5614 in combination with tyrosine kinase inhibitors in chronic phase chronic myelogenous leukemia patients

Harigae Hideo0 个研究点目标入组 60 人开始时间: 2022年5月25日最近更新:
适应症

试验速览

阶段
3 期
状态
进行中(未招募)
发起方
入组人数
60

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
>= 18age old 至 ot applicable(—)
性别
All

入选标准

  • (1) Patient aged 18y or older
  • (2) Signed informed consent
  • (3) Patient with Philadelphia chromosome positive chronic phase CML and Major BCR-ABL1 transcript positivity
  • (4) Treatment with imatinib, nilotinib, dasatinib or bosutinib for more than 3 years and less than 6 years
  • (5) No switch between TKIs within the last 12 weeks
  • (6) No dose modification of TKI within the last 12 weeks
  • (7) BCR-ABL(IS) <= 0.1%
  • (8) BCR-ABL(IS) > 0.0032%
  • (9) ECOG PS grade 0 to 2
  • (10) AST and ALT <= 2.5 times the upper limit of the reference value
  • (11) Bilirubin in serum <= 2.5 times the upper limit of the reference value
  • (12) Men and Women of childbearing potential must be using an adequate method of contraception

排除标准

  • (1) Pregnant or lactating women
  • (2) Participation in another clinical trial with any investigative drug within 30 days prior to study enrolment,
  • (3) Prior history of hematopoietic stem cell transplantation (autologous or allogenic)
  • (4) Cardiovascular disease:
  • - Stage II to IV congestive heart failure as determined by the NYHA classification system for heart failure
  • - Myocardial infarction within the previous 6 months
  • - Symptomatic arrhythmias that need treatment
  • (5) Known T315I BCR-ABL kinase domain mutation
  • (6) CML patient not in chronic phase at diagnosis
  • (7) Patients with an active malignancy
  • (8) Known HIV-positivity
  • (9) Patients with bleeding tendency
  • (10) Other patients whom a lead investigator or the patient's primary physician deems are not appropriate for this study

研究者

发起方
Harigae Hideo

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