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About VORANIGO®

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A new treatment option for your patients with IDH1/2-mutant glioma

The FIRST and ONLY oral IDH inhibitor indicated in the treatment of Grade 2 astrocytoma or oligodendroglioma with a susceptible IDH1/2 mutation*,1–3

VORANIGO® (vorasidenib tablets) is indicated for the treatment of Grade 2a astrocytoma or oligodendroglioma with a susceptible isocitrate dehydrogenase-1 (IDH1) mutation or isocitrate dehydrogenase-2 (IDH2) mutation in adults and pediatric patients aged 12 years and older following surgical intervention.

Treatment with VORANIGO® should be initiated following confirmation of an IDH1 or IDH2 mutation through a validated test.

a WHO 2016, 2021 grading system.

Mechanism of action: An inhibitor of IDH1 and IDH2 enzymes†,1

VORANIGO®:

  • Inhibited IDH1 and IDH2 wild type and variants in vitro and in vivo tumour models expressing IDH1 or IDH2 proteins
  • Decreased 2-HG production and may restore cellular differentiation

VORANIGO® decreases 2-HG tumour concentrations in patients with IDH1 or IDH2 mutated glioma.

Graph presenting Voranigo mechanism of action

Adapted from the VORANIGO® Product Monograph.

VORANIGO® resources

VORANIGO® information leaflet

An overview of VORANIGO® in the treatment of IDH1/2-mutant glioma, including efficacy and safety data, as well as dosing and administration information.

WHO: World Health Organization; mIDH1/2: mutant IDH1/2; 2H-G: 2-hydroxyglutarate

*Comparative clinical significance has not been established.

†Clinical significance is unknown.

References:

  1. VORANIGO® Product Monograph. Servier Canada. August 27, 2024.
  2. Mellinghoff IK et al. Vorasidenib in IDH1- or IDH2-mutant low-grade glioma. N Engl J Med. 2023;389(7):589–601.
  3. Data on file. Servier Canada Inc.

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