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临床试验/JPRN-jRCT2080221799
JPRN-jRCT2080221799未知1 期

A Phase 1 Study of MLN8237 in Japanese Patients with Relapsed and/or Refractory Non-Hodgkin's lymphoma

Takeda Pharmaceutical Company Limited0 个研究点目标入组 24 人开始时间: 2012年5月25日最近更新:
适应症

试验速览

阶段
1 期
入组人数
24

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
>= 20age old 至 <= 75age old(—)
性别
All

入选标准

  • 1) Patients with relapsed and/or refractory Non-Hodgkin's Lymphoma that is diagnosed hisologically or cytologically
  • 2) Patients with radiologically or clinically measurable diseases
  • 3) Eastern Cooperative Oncology Group (ECOG) Performance Status (PS) of 0 to 1

排除标准

  • 1) Prior treatment with Aurora kinase inhibitors
  • 2) Prior treatment of allogeneic hematopoietic stem cells transplant, or organ transplant
  • 3) Patients with brain or cerebrospinal invasion
  • 4) Major surgery within 14 days prior to enrollment
  • 5) Serious infection or infection that requires intravenous antibiotics within 14 days prior to enrollment.
  • 6) Simultaneously diagnosed with or treated for another malignancy, or having a clinical history of primary malignancy in another organ(s)

研究者

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