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A Study to Explore Treatment Patterns, Treatment Outcomes, Healthcare Resource Utilization in Adult Participants With Myelofibrosis Through Chart Review

Completed
Conditions
Myelofibrosis
Registration Number
NCT05444972
Lead Sponsor
AbbVie
Brief Summary

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.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
998
Inclusion Criteria
  • 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.
Exclusion Criteria
  • Having received MF treatment in a clinical trial setting.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Time from Diagnosis of Myelofibrosis (MF) to Initial TreatmentUp to Week 156

Time from diagnosis of MF to initial treatment.

Duration of Second TreatmentUp to Week 156

Duration of second treatment.

Duration of Initial TreatmentUp to Week 156

Duration of initial treatment.

Duration of Subsequent TreatmentsUp to Week 156

Duration of subsequent treatments.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (66)

UAB Comprehensive Cancer Center /ID# 252767

🇺🇸

Birmingham, Alabama, United States

Wellness Oncology & Hematology /ID# 255591

🇺🇸

West Hills, California, United States

Brigham & Women's Hospital /ID# 254312

🇺🇸

Boston, Massachusetts, United States

Gabrail Cancer Center Research /ID# 252768

🇺🇸

Canton, Ohio, United States

Instituto FIDES /ID# 245526

🇦🇷

La Plata, Buenos Aires, Argentina

Hospital Italiano de Buenos Aires /ID# 244373

🇦🇷

Ciudad Autonoma Buenos Aires, Ciuadad Autonoma De Buenos Aires, Argentina

Fundaleu /Id# 244371

🇦🇷

Ciudad Autonoma de Buenos Aire, Ciuadad Autonoma De Buenos Aires, Argentina

Townsville University Hospital /ID# 246585

🇦🇺

Douglas, Queensland, Australia

Royal Adelaide Hospital /ID# 246583

🇦🇺

Adelaide, South Australia, Australia

Fiona Stanley Hospital /ID# 246584

🇦🇺

Murdoch, Western Australia, Australia

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UAB Comprehensive Cancer Center /ID# 252767
🇺🇸Birmingham, Alabama, United States

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