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Recruiting NCT07774455

Pacritinib Effectiveness in Real-world Settings

Conditions: Myelofibrosis (MF)

Sex: All
Ages: 18 Years – N/A
Healthy volunteers: No
Enrollment: 60
Sponsor: Swedish Orphan Biovitrum

Location: Yale School of Medicine New Haven Connecticut

Summary

This study aims to evaluate real-world treatment patterns and effectiveness of pacritinib, including hematologic and clinical outcomes, and survival through a site-based retrospective chart review of medical records of patients with MF.

Eligibility Criteria

Inclusion Criteria: * Adult patients must be ≥18 years of age at the index date * Patients diagnosed with MF with platelet counts ≥50 x 109/L at the time of treatment initiation with pacritinib. If multiple values are available within 30 days prior to initiating treatment with pacritinib will use the value closest to index date * Patients will be required to have ≥1 month of treatment with pacritinib and ≥6 months of observation from the start of pacritinib unless the patient died within 6 months of starting pacritinib * If peripheral blasts were evaluated prior to index, they must be \

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View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT07774455). StuddyBuddy aggregates publicly available trial information.