KLERTIS

This brand name is authorized in Lithuania, Poland, Romania

Active ingredients

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

1 Sunitinib
UNII V99T50803M - SUNITINIB

Sunitinib inhibits multiple RTKs that are implicated in tumour growth, neoangiogenesis, and metastatic progression of cancer.

Read about Sunitinib

Medicine classification

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

ATC code Group title Classification
L01EX01 Sunitinib L Antineoplastic and immunomodulating agents → L01 Antineoplastic agents → L01E Protein kinase inhibitors → L01EX Other protein kinase inhibitors
Discover more medicines within L01EX01

Authorization and marketing

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

Country Identification scheme Identifier(s)
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1092557, 1092558, 1092559, 1092560, 1092561, 1092562
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100430074, 100430080, 100430097
Country: RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale Identifier(s): W68008001, W68008002, W68009001, W68009002, W68010001, W68010002

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