Bosutinib: Pediatric First Approval

Paediatr Drugs. 2024 Mar;26(2):209-214. doi: 10.1007/s40272-023-00608-4.

Abstract

Bosutinib (BOSULIF®), an orally administered BCR-ABL tyrosine kinase inhibitor (TKI) developed by Pfizer Inc., is well established in the EU and the USA as a treatment for adults with newly diagnosed (ND) chronic phase (CP) Philadelphia chromosome-positive (Ph+) chronic myelogenous leukemia (CML), and for CP, accelerated phase and blast phase Ph+ CML that is resistant or intolerant (R/I) to prior therapy. In September 2023, based on clinical data from patients aged ≥ 1 to < 18 years, bosutinib was approved in the USA for the treatment of pediatric patients aged ≥ 1 year with CP Ph+ CML that is ND or R/I to prior therapy. This article summarizes the milestones in the development of bosutinib leading to this first pediatric approval.

Publication types

  • Review

MeSH terms

  • Adult
  • Aniline Compounds* / adverse effects
  • Child
  • Humans
  • Nitriles / adverse effects
  • Protein Kinase Inhibitors / adverse effects
  • Quinolines* / adverse effects

Substances

  • bosutinib
  • Aniline Compounds
  • Nitriles
  • Quinolines
  • Protein Kinase Inhibitors