EBGLYSS

This brand name is authorized in United States. It is also authorized in Austria, Croatia, Estonia, France, Ireland, Italy, Lithuania, Spain, UK.

Active ingredients

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

1
UNII U9JLP7V031 - LEBRIKIZUMAB
 

Lebrikizumab is an immunoglobulin (IgG4) monoclonal antibody that binds with high affinity to interleukin (IL)-13 and selectively inhibits IL-13 signalling through the IL-4 receptor alpha (IL-4Rα)/ IL-13 receptor alpha 1 (IL-13Rα1) heterodimer, thereby inhibiting the downstream effects of IL-13. Inhibition of IL-13 signalling is expected to be of benefit in diseases in which IL-13 is a key contributor to the disease pathogenesis. Lebrikizumab does not prevent the binding of IL-13 to the IL-13 receptor alpha 2 (IL-13Rα2 or decoy receptor), which allows the internalisation of IL-13 into the cell.

 
Read more about Lebrikizumab

Medication package inserts

Below package inserts are available for further reading:

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

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 3055980, 3055991, 3056004, 3056015, 3056026, 3056037, 3056048, 3056059, 3056060, 3056071, 3056082, 3056093
ES Centro de información online de medicamentos de la AEMPS 1231765001, 1231765007
FR Base de données publique des médicaments 63696560, 65119162
IT Agenzia del Farmaco 050964016, 050964028, 050964030, 050964042, 050964079, 050964081, 050964093, 050964105, 050964117, 050964129
LT Valstybinė vaistų kontrolės tarnyba 1098146, 1098147, 1098148, 1098149, 1098150, 1098151, 1098152, 1098153, 1098154, 1098155, 1098156, 1098157
US FDA, National Drug Code 0002-7772, 0002-7797

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