AYVAKYT

This brand name is authorized in Austria, Croatia, Estonia, France, Ireland, Lithuania, Poland, Romania, UK.

Active ingredients

The drug AYVAKYT contains one active pharmaceutical ingredient (API):

1
UNII 513P80B4YJ - AVAPRITINIB
 

Avapritinib is a Type 1 kinase inhibitor that has demonstrated biochemical in vitro activity on the PDGFRA D842V and KIT D816V mutants associated with resistance to imatinib, sunitinib and regorafenib with half maximal inhibitory concentrations (IC50) of 0.24 nM and 0.27 nM, respectively, and greater potency against clinically relevant KIT exon 11, KIT exon 11/17 and KIT exon 17 mutants than against the KIT wild-type enzyme.

 
Read more about Avapritinib

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 AYVAKYT Film-coated tablet MPI, EU: SmPC European Medicines Agency (EU)

Medicine classification

This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:

ATC Group Classification
L01EX18 L Antineoplastic and immunomodulating agents → L01 Antineoplastic agents → L01E Protein kinase inhibitors → L01EX Other protein kinase inhibitors
Discover more medicines within L01EX18

Authorization and marketing

This drug has been assigned below unique identifiers within the countries it is being marketed:

Country Identification scheme Identifier(s)
EE Ravimiamet 1828201, 1828212, 1828223, 1878509, 1878510
FR Base de données publique des médicaments 63189920, 64069767, 65304816
GB Medicines & Healthcare Products Regulatory Agency 390640, 390643, 390648
LT Valstybinė vaistų kontrolės tarnyba 1091244, 1091245, 1091246
PL Rejestru Produktów Leczniczych 100441847, 100441853, 100441860
RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale W69470001, W69471001, W69472001, W69473001, W69474001

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