跳至主要内容
临床试验/NCT05444972
NCT05444972已完成不适用

A Multi-Country, Real-World Study to Explore Treatment Patterns, Effectiveness and Healthcare Resource Utilization for Patients Diagnosed With Myelofibrosis Through Chart Review

AbbVie66 个研究点 分布在 10 个国家目标入组 998 人开始时间: 2022年8月23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
入组人数
998
试验地点
66
主要终点
Time from Diagnosis of Myelofibrosis (MF) to Initial Treatment

研究概览

简要总结

Myelofibrosis (MF) is a rare blood cancer, characterized by extensive fibrosis (scarring) of the bone marrow. It is one of a group of cancers known as myeloproliferative neoplasms (MPNs) in which bone marrow cells that produce blood cells develop and function abnormally. This study will evaluate treatment patterns, treatment outcomes, healthcare resource utilization in adult participants with Myelofibrosis.

Data from approximately 1000 participants will be collected. No participants will be enrolled in this study.

Participants' charts will be reviewed. No drug will be administered as a part of this study. The duration of the observation period is up to 156 weeks.

There is no additional burden for participants in this trial. All visits must be completed prior to data extraction and participants will be followed for up to 156 weeks.

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

入选标准

  • Treated for myelofibrosis (MF) [primary myelofibrosis (PMF) and secondary myelofibrosis (SMF)].
  • Must have initiated their first treatment on or after the first date when ruxolitinib was approved in their country of residence and no later than 31 December 2021.

排除标准

  • Having received MF treatment in a clinical trial setting.

结局指标

主要结局

Time from Diagnosis of Myelofibrosis (MF) to Initial Treatment

时间窗: Up to Week 156

Time from diagnosis of MF to initial treatment.

Duration of Second Treatment

时间窗: Up to Week 156

Duration of second treatment.

Duration of Initial Treatment

时间窗: Up to Week 156

Duration of initial treatment.

Duration of Subsequent Treatments

时间窗: Up to Week 156

Duration of subsequent treatments.

次要结局

未报告次要终点

研究者

发起方
AbbVie
申办方类型
Industry
责任方
Sponsor

研究点 (66)

Loading locations...

相似试验