跳至主要内容
临床试验/NCT05833022
NCT05833022已完成不适用

Patient Characteristics and Treatment Patterns From Early Crizanlizumab Use in Real-world Setting: Preliminary Analysis From Select Sickle Cell Centers

Novartis Pharmaceuticals11 个研究点 分布在 1 个国家目标入组 297 人开始时间: 2021年7月30日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
297
试验地点
11
主要终点
Percentage of patients who received sickle cell disease treatment (use of hydroxyurea, l-glutamine, chronic transfusion therapy, and voxelotor) during treatment with crizanlizumab

研究概览

简要总结

This was a retrospective cohort study using secondary data from member sites of the National Alliance of Sickle Cell Centers (NASCC) with at least five patients who initiated crizanlizumab. Patients who were prescribed crizanlizumab were included in the cohort.

研究设计

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

入排标准

年龄范围
16 Years 至 —(Child, 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

Percentage of patients who received sickle cell disease treatment (use of hydroxyurea, l-glutamine, chronic transfusion therapy, and voxelotor) during treatment with crizanlizumab

时间窗: Up to 12 months

Percentage of patients who received sickle cell disease treatment (use of hydroxyurea, l-glutamine, chronic transfusion therapy, and voxelotor) prior to treatment with crizanlizumab

时间窗: Up to 12 months

次要结局

  • Number of doses of crizanlizumab for patients who discontinued treatment with crizanlizumab(Up to 24 months)
  • Number of sickle cell disease (SCD)-related hospitalizations(Up to 24 months)
  • Number of patients who discontinued treatment with crizanlizumab(Up to 24 months)
  • Reasons for early discontinuation of crizanlizumab treatment(Up to 24 months)
  • Number of SCD-related emergency department (ED) visits(Up to 24 months)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (11)

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