KYNTHEUM

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

Active ingredients

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

1 Brodalumab
UNII 6ZA31Y954Z - BRODALUMAB

Brodalumab is a recombinant fully human monoclonal immunoglobulin IgG2 antibody that binds with high affinity to human IL-17RA and blocks the biological activities of the pro-inflammatory cytokines IL-17A, IL-17F, IL-17A/F heterodimer and IL-25, resulting in inhibition of the inflammation and clinical symptoms associated with psoriasis.

Read about Brodalumab

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
KYNTHEUM 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
L04AC12 L Antineoplastic and immunomodulating agents → L04 Immunosuppressants → L04A Immunosuppressants → L04AC Interleukin inhibitors
Discover more medicines within L04AC12

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): 1750205, 1777956
Country: ES Centro de información online de medicamentos de la AEMPS Identifier(s): 1161155001
Country: FI Lääkealan turvallisuus- ja kehittämiskeskus Identifier(s): 568224
Country: FR Base de données publique des médicaments Identifier(s): 65620419
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 346264
Country: IE Health Products Regulatory Authority Identifier(s): 88881
Country: IT Agenzia del Farmaco Identifier(s): 045484019, 045484021
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1083403, 1084580
Country: NL Z-Index G-Standaard, PRK Identifier(s): 146757
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100417955

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