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Valoctocogene roxaparvovec

Valoctocogene roxaparvovec is a medicine in the class miscellaneous. It is used for hemophilia a.

Dernière mise à jour Sources: EMA SmPC

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L'essentiel

Classe médicamenteuse
Miscellaneous
Code ATC
B02BD15
Interactions connues
40 (Majeure: 6 · Modérée: 33 · Mineure: 1)
Noms commerciaux
1
Pays et marchés
1

Indications

Mécanisme d'action

AAV5-based gene therapy vector that expresses B-domain deleted SQ recombinant human factor VIII (hFVIII-SQ) under a liver-specific promoter, replacing the missing factor VIII. Vector DNA forms episomal transgenes that support long-term hFVIII-SQ production.

Posologie adulte habituelle (résumé de la notice)

Severe haemophilia A: 6 × 1013 vg/kg body weight, intravenous, as a single infusion. Dose volume in mL = body weight in kg multiplied by 3.

Résumé de la notice pour la première ligne de posologie uniquement ; les sections complètes sur la posologie figurent dans l'application.

Grossesse et allaitement

Grossesse
Unsafe Gene therapy for men with severe haemophilia A. No pregnancy data or animal studies; theoretical risk of vector DNA reaching fetal cells. EU label: should not be used in pregnancy; not recommended in women who could become pregnant. Partners of treated men: double-barrier contraception for 6 months.
Allaitement
Unknown Not known if the vector or factor VIII it produces passes into milk; no LactMed record. EU label: a risk to the infant cannot be excluded; should not be used while breastfeeding. It is licensed for men, so use while breastfeeding is not expected.

Effets indésirables signalés

  • ALT increased
  • AST increased
  • LDH increased
  • CPK increased
  • Nausea
  • Headache

Contre-indications

  • Hypersensitivity to the active substance or any excipient.
  • Active infections (acute or uncontrolled chronic), or known significant hepatic fibrosis or cirrhosis.

Précautions particulières

  • Only for patients demonstrated to lack anti-AAV5 antibodies by a validated assay; not indicated with a history of factor VIII inhibitors.
  • Hepatic reactions (ALT increase) occur in most patients; monitor ALT and factor VIII activity and give corticosteroids as needed.
  • Infusion-related reactions can occur; monitor during and after infusion.

Informez votre pharmacien ou votre médecin en cas de grossesse ou d'allaitement, de maladie rénale ou hépatique, d'allergies, ainsi que de tout autre médicament ou complément que vous prenez.

Principales interactions (40)

All 40 interactions, with severity and what to do

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  • Dosing by age, kidney and liver function, and further dose lines
  • Renal and hepatic dose adjustments
  • Dosing in older adults
  • How to give it
  • Pharmacokinetics
  • Patient counselling points
  • Food interactions
  • IV preparation and dilution

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Questions fréquentes

What is Valoctocogene roxaparvovec used for?

Valoctocogene roxaparvovec is a medicine in the class miscellaneous. It is used for Hemophilia a.

What side effects have been reported with Valoctocogene roxaparvovec?

ALT increased, AST increased, LDH increased, CPK increased, Nausea, Headache.

Can Valoctocogene roxaparvovec be taken in pregnancy or while breastfeeding?

Pregnancy: Unsafe. Gene therapy for men with severe haemophilia A. No pregnancy data or animal studies; theoretical risk of vector DNA reaching fetal cells. EU label: should not be used in pregnancy; not recommended in women who could become pregnant. Partners of treated men: double-barrier contraception for 6 months. Breastfeeding: Unknown. Not known if the vector or factor VIII it produces passes into milk; no LactMed record. EU label: a risk to the infant cannot be excluded; should not be used while breastfeeding. It is licensed for men, so use while breastfeeding is not expected.

What does Valoctocogene roxaparvovec interact with?

MediHelp lists 40 known interactions for Valoctocogene roxaparvovec. Major: 6 · Moderate: 33 · Minor: 1. The most serious include Dantrolene, Efavirenz, Flutamide.

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