Pacritinib

(Vonjo®)

Vonjo®

Drug updated on 11/5/2024

Dosage FormCapsule (oral; 100 mg)
Drug ClassKinase inhibitors
Ongoing and
Completed Studies
ClinicalTrials.gov

Indication

  • Indicated for the treatment of adults with intermediate or highrisk primary or secondary (post-polycythemia vera or post-essential thrombocythemia) myelofibrosis with a platelet count below 50 109 /L

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Summary
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  • This summary is based on the review of one systematic review(s)/meta-analysis(es). [1]
  • Pacritinib is less effective than ruxolitinib as a first-line treatment for reducing spleen volume, but it shows effectiveness in second-line treatment after ruxolitinib exposure.
  • Fedratinib and momelotinib have comparable efficacy to ruxolitinib for spleen volume reduction in first-line therapy.
  • Pacritinib is noted for its second-line effectiveness after ruxolitinib, while no second-line data is provided for fedratinib or momelotinib.
  • There is no safety information available in the reviewed documents.
  • There is no population types or subgroups information available in the reviewed documents.

Product Monograph / Prescribing Information

Document TitleYearSource
Vonjo (pacritinib) Prescribing Information.2023CTI BioPharma Corp., Seattle WA

Systematic Reviews / Meta-Analyses

Clinical Practice Guidelines

Document TitleYearSource
Myeloproliferative Neoplasms, Version 3.2022, NCCN Clinical Practice Guidelines in Oncology.2022Journal of the National Comprehensive Cancer Network