ZYKADIA

This brand name is authorized in United States. It is also authorized in Australia, Austria, Canada, Estonia, France, Hong Kong SAR China, Ireland, Japan, Lithuania, Netherlands, Poland, Romania, Singapore, Spain, Turkey, UK.

Active ingredients

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

1
UNII K418KG2GET - CERITINIB
 

Ceritinib is an orally highly selective and potent ALK inhibitor. Ceritinib inhibits autophosphorylation of ALK, ALK-mediated phosphorylation of downstream signalling proteins and proliferation of ALK-dependent cancer cells both in vitro and in vivo.

 
Read more about Ceritinib

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 ZYKADIA Hard capsule 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
L01ED02 L Antineoplastic and immunomodulating agents → L01 Antineoplastic agents → L01E Protein kinase inhibitors → L01ED Anaplastic lymphoma kinase (ALK) inhibitors
Discover more medicines within L01ED02

Authorization and marketing

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

Country Identification scheme Identifier(s)
AU Pharmaceutical Benefits Scheme 11056X
CA Health Products and Food Branch 02436779
EE Ravimiamet 1684560, 1697115, 1766088, 1792559
ES Centro de información online de medicamentos de la AEMPS 115999001
FR Base de données publique des médicaments 66958808
GB Medicines & Healthcare Products Regulatory Agency 379924
HK Department of Health Drug Office 64236
IE Health Products Regulatory Authority 88742
JP 医薬品医療機器総合機構 4291044F1022
LT Valstybinė vaistų kontrolės tarnyba 1076640, 1078234, 1084938, 1087492
NL Z-Index G-Standaard, PRK 125938, 199608
PL Rejestru Produktów Leczniczych 100342909, 100433606
RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale W64628001, W64628002
SG Health Sciences Authority 14776P
TR İlaç ve Tıbbi Cihaz Kurumu 8699504152050
US FDA, National Drug Code 0078-0694

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