Midostaurin: First Global Approval

Drugs. 2017 Jul;77(11):1251-1259. doi: 10.1007/s40265-017-0779-0.

Abstract

Midostaurin (Rydapt®) is a multikinase inhibitor being developed by Novartis Pharmaceuticals. In April 2017, midostaurin was approved in the USA for the treatment of adult patients with newly diagnosed, FMS-like tyrosine kinase 3 (FLT3) mutation-positive acute myeloid leukaemia (AML) [in combination with standard cytarabine and daunorubicin induction, and cytarabine consolidation], or aggressive systemic mastocytosis (ASM), systemic mastocytosis with associated haematological neoplasm (SM-AHN) or mast cell leukaemia (MCL) [collectively known as advanced SM]. The article summarizes the milestones in the development of midostaurin leading to this first global approval.

Publication types

  • Review

MeSH terms

  • Adolescent
  • Adult
  • Clinical Trials as Topic
  • Drug Approval
  • Humans
  • Leukemia, Mast-Cell / drug therapy*
  • Leukemia, Myeloid, Acute / drug therapy*
  • Mastocytosis, Systemic / drug therapy*
  • Middle Aged
  • Protein Kinase Inhibitors / therapeutic use*
  • Staurosporine / administration & dosage
  • Staurosporine / adverse effects
  • Staurosporine / analogs & derivatives*
  • Staurosporine / pharmacokinetics
  • Staurosporine / therapeutic use
  • United States
  • United States Food and Drug Administration
  • Young Adult

Substances

  • Protein Kinase Inhibitors
  • Staurosporine
  • midostaurin