IMLYGIC

This brand name is authorized in Austria, Estonia, Finland, France, Croatia, Ireland, Israel, Italy, Lithuania, Netherlands, Poland, United Kingdom, United States

Active ingredients

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

1 Talimogene laherparepvec
UNII 07730V90L6 - TALIMOGENE LAHERPAREPVEC

Talimogene laherparepvec is an oncolytic immunotherapy that is derived from HSV-1. Talimogene laherparepvec has been modified to replicate within tumours and to produce the immune stimulatory protein human GM-CSF. Talimogene laherparepvec causes the death of tumour cells and the release of tumour-derived antigens.

Read about Talimogene laherparepvec

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
IMLYGIC Solution for injection European Medicines Agency (EU) MPI, EU: SmPC

Medicine classification

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

ATC code Group title Classification
L01XL02 L Antineoplastic and immunomodulating agents → L01 Antineoplastic agents → L01X Other antineoplastic agents → L01XL Antineoplastic cell and gene therapy
Discover more medicines within L01XL02

Authorization and marketing

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

Country Identification scheme Identifier(s)
Country: EE Ravimiamet Identifier(s): 1708590, 1708602
Country: FI Lääkealan turvallisuus- ja kehittämiskeskus Identifier(s): 050826, 475527
Country: FR Base de données publique des médicaments Identifier(s): 65763328, 67792809
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 348715, 348717
Country: IL מִשְׂרַד הַבְּרִיאוּת Identifier(s): 8509, 8510
Country: IT Agenzia del Farmaco Identifier(s): 044653018, 044653020
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1079249, 1079250
Country: NL Z-Index G-Standaard, PRK Identifier(s): 130346, 130354
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100362830, 100362846
Country: US FDA, National Drug Code Identifier(s): 55513-078, 55513-079

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