TEPMETKO

This brand name is authorized in United States. It is also authorized in Austria, Brazil, Croatia, Estonia, Finland, Israel, Italy, Japan, Lithuania, Poland.

Active ingredients

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

1
UNII VY5YX2TQ1F - TEPOTINIB HYDROCHLORIDE
 

Tepotinib is a reversible Type I adenosine triphosphate (ATP)-competitive small molecule inhibitor of MET. Tepotinib blocked MET phosphorylation and MET-dependent downstream signalling in a dose-dependent manner. Tepotinib demonstrated pronounced anti-tumour activity in tumours with oncogenic activation of MET, such as METex14 skipping alterations.

 
Read more about Tepotinib

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 TEPMETKO Film-coated tablet MPI, EU: SmPC European Medicines Agency (EU)
 TEPMETKO Film-coated tablet MPI, US: SPL/PLR FDA, National Drug Code (US)

Medicine classification

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

ATC Group Classification
L01EX21 L Antineoplastic and immunomodulating agents → L01 Antineoplastic agents → L01E Protein kinase inhibitors → L01EX Other protein kinase inhibitors
Discover more medicines within L01EX21

Authorization and marketing

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

Country Identification scheme Identifier(s)
BR Câmara de Regulação do Mercado de Medicamentos 525421090053002
EE Ravimiamet 1876293
FI Lääkealan turvallisuus- ja kehittämiskeskus 176387
IL מִשְׂרַד הַבְּרִיאוּת 9037
IT Agenzia del Farmaco 049967019
JP 医薬品医療機器総合機構 4291065F1024
LT Valstybinė vaistų kontrolės tarnyba 1094284
PL Rejestru Produktów Leczniczych 100466998
US FDA, National Drug Code 44087-5000

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