ILUMETRI

This brand name is authorized in Austria, Estonia, Spain, France, Ireland, Lithuania, Netherlands, Poland, Romania, United Kingdom

Active ingredients

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

1 Tildrakizumab
UNII DEW6X41BEK - TILDRAKIZUMAB

Tildrakizumab is a humanized IgG1/k monoclonal antibody that specifically binds to the p19 protein subunit of the interleukin-23 (IL-23) cytokine without binding to IL-12 and inhibits its interaction with the IL-23 receptor. Tildrakizumab inhibits the release of proinflammatory cytokines and chemokines.

Read about Tildrakizumab

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
ILUMETRI 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
L04AC17 L Antineoplastic and immunomodulating agents → L04 Immunosuppressants → L04A Immunosuppressants → L04AC Interleukin inhibitors
Discover more medicines within L04AC17

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): 1780130, 1780488
Country: ES Centro de información online de medicamentos de la AEMPS Identifier(s): 1181323001
Country: FR Base de données publique des médicaments Identifier(s): 69596271
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 364267, 367558
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1086234, 1086387
Country: NL Z-Index G-Standaard, PRK Identifier(s): 198293
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100411378
Country: RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale Identifier(s): W66238001, W66238002

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