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临床试验/NCT01235117
NCT01235117已完成2 期

A Phase 2 Study of Azacitidine in Chronic Myelomonocytic Leukemia (CMML)

University of Leeds4 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2010年1月最近更新:
适应症
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
30
试验地点
4
主要终点
Safety and tolerability

研究概览

简要总结

RATIONALE: Drugs used in chemotherapy, such as azacitidine, work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing.

PURPOSE: This phase II trial is studying the side effects of azacitidine and to see how well it works in treating patients with chronic myelomonocytic leukemia.

详细描述

OBJECTIVES:

Primary

  • To assess the safety and tolerability of azacitidine in patients with chronic myelomonocytic leukemia (CMML).
  • To assess the overall response rate in these patients.

Secondary

  • To assess the incidence of clinical remission/complete remission or partial response in these patients.
  • To assess hematological improvement in patients treated with this drug.
  • To assess the overall survival of patients treated with this drug.
  • To assess progression-free survival of patients treated with this drug.
  • To assess the time to acute myeloid leukemia (AML) transformation of CMML.
  • To assess the time to death or AML transformation of CMML.
  • To assess the biological correlates.

研究设计

研究类型
Interventional
分配方式
Non Randomized
主要目的
Treatment

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

结局指标

主要结局

Safety and tolerability

Overall response rate

次要结局

  • Incidence of clinical remission/complete remission or partial response according to International Working Group (IWG) criteria
  • Progression-free survival
  • Time to acute myeloid leukemia (AML) transformation of CMML
  • Hematological improvement according to IWG criteria
  • Overall survival
  • Time to death or AML transformation of CMML
  • Biological correlates

研究者

申办方类型
Other

研究点 (4)

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