跳至主要内容
临床试验/NCT02783651
NCT02783651已完成不适用

An Observational Study of Patients With Philadelphia Chromosome-negative Relapsed or Refractory Acute Lymphoblastic Leukemia in the US

Amgen1 个研究点 分布在 1 个国家目标入组 212 人开始时间: 2016年6月30日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
Amgen
入组人数
212
试验地点
1
主要终点
Drug utilization in patients with Ph- R/R ALL

研究概览

简要总结

A retrospective chart review study of Philadelphia chromosome-negative R/R ALL patients in the US.

研究设计

研究类型
Observational
观察模型
Other
时间视角
Retrospective

入排标准

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

Drug utilization in patients with Ph- R/R ALL

时间窗: 86 months

Treatment patterns in patients with Ph- R/R ALL

时间窗: 86 months

Healthcare resource utilization in patients with Ph- R/R ALL

时间窗: 86 months

次要结局

  • Incidence of selected adverse events including cytokine release syndrome, neurologic events, any events resulting in hospitalizations, and other serious adverse events.(86 Months)
  • RFS from time remission achieved with salvage treatment(86 Months)
  • MRD status within 12 weeks of initiation of salvage treatment(12 Weeks)
  • Overall survival from the time of initiation of salvage treatment(86 Months)
  • Receipt of allogeneic stem cell transplantation following salvage treatment(86 Months)
  • Best response to salvage treatment (chemotherapy or blinatumomab) within 8 weeks and within 12 weeks of initiation of salvage treatment.(12 Weeks)

研究者

发起方
Amgen
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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