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临床试验/JPRN-jRCT2080223611
JPRN-jRCT2080223611已完成3 期

A Phase 3, Double-Blind, Placebo-controlled Study of Quizartinib Administered in Combination with Induction and Consolidation Chemotherapy, and Administered as Continuation Therapy in Subjects with Newly Diagnosed FLT3 ITD (+) Acute Myeloid Leukemia

DAIICHI SANKYO CO., LTD.0 个研究点目标入组 35 人开始时间: 2017年8月8日最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
入组人数
35

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.Newly diagnosed, morphologically documented primary AML or AML secondary to myelodysplastic syndrome or a myeloproliferative neoplasm (at Screening)
  • 2.Eastern Cooperative Oncology Group performance status 0-2 (at Screening)

排除标准

  • 1.Diagnosis of acute promyelocytic leukemia (APL), chronic myelogenous leukemia in blast crisis
  • 2.Active acute or chronic systemic fungal, bacterial, or viral infection not well controlled by antifungal, antibacterial or antiviral therapy

研究者

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