KISPLYX

This brand name is authorized in Austria, Croatia, Estonia, Finland, Ireland, Italy, Lithuania, Netherlands, Poland, Romania, Spain, UK.

Active ingredients

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

1	Lenvatinib UNII 3J78384F61 - LENVATINIB MESYLATE
	Lenvatinib is a receptor tyrosine kinase (RTK) inhibitor that selectively inhibits the kinase activities of vascular endothelial growth factor (VEGF) receptors VEGFR1 (FLT1), VEGFR2 (KDR), and VEGFR3 (FLT4), in addition to other proangiogenic and oncogenic pathway-related RTKs including fibroblast growth factor (FGF) receptors FGFR1, 2, 3, and 4, the platelet derived growth factor (PDGF) receptor PDGFRα, KIT, and RET.
	Read more about Lenvatinib

Medication package inserts

Below package inserts are available for further reading:

Document	Type	Information Source
KISPLYX Hard capsule	MPI, EU: SmPC	Medicines & Healthcare Products Regulatory Agency (GB)

Medicine classification

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

ATC Group		Classification
L01EX08		L Antineoplastic and immunomodulating agents → L01 Antineoplastic agents → L01E Protein kinase inhibitors → L01EX Other protein kinase inhibitors
Discover more medicines within L01EX08

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	1728378, 1728389, 1821787, 1821798, 1821800, 1821811
ES	Centro de información online de medicamentos de la AEMPS	1161128001, 1161128002
FI	Lääkealan turvallisuus- ja kehittämiskeskus	453579, 467073
GB	Medicines & Healthcare Products Regulatory Agency	335615, 335617
IT	Agenzia del Farmaco	045060011, 045060023, 045060035, 045060047, 045060050, 045060062
LT	Valstybinė vaistų kontrolės tarnyba	1080867, 1080868, 1088910, 1088911, 1088912, 1088913
NL	Z-Index G-Standaard, PRK	133256, 133299
PL	Rejestru Produktów Leczniczych	100377486, 100377492
RO	Agenția Națională a Medicamentului și a Dispozitivelor Medicale	W68099001, W68099002, W68099003, W68100001, W68100002, W68100003