BAVENCIO

This brand name is authorized in United States. It is also authorized in Australia, Austria, Brazil, Canada, Croatia, Estonia, Finland, France, Hong Kong SAR China, Ireland, Israel, Japan, Lithuania, Netherlands, Poland, Romania, Singapore, Spain, Turkey, UK.

Active ingredients

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

1
UNII KXG2PJ551I - AVELUMAB
 

Avelumab is a human immunoglobulin G1 (IgG1) monoclonal antibody directed against programmed death ligand 1 (PD-L1). Avelumab binds PD-L1 and blocks the interaction between PD-L1 and the programmed death 1 (PD-1) and B7.1 receptors. This removes the suppressive effects of PD-L1 on cytotoxic CD8+ T-cells, resulting in the restoration of anti-tumour T-cell responses.

 
Read more about Avelumab

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 BAVENCIO Concentrate for solution for infusion MPI, EU: SmPC European Medicines Agency (EU)

Medicine classification

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

ATC Group Classification
L01FF04 Avelumab L Antineoplastic and immunomodulating agents → L01 Antineoplastic agents → L01F Monoclonal antibodies and antibody drug conjugates → L01FF PD-1/PDL-1 (Programmed cell death protein 1/death ligand 1) inhibitors
Discover more medicines within L01FF04

Authorization and marketing

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

Country Identification scheme Identifier(s)
AU Pharmaceutical Benefits Scheme 11671G, 11679Q, 11685B, 11695M
BR Câmara de Regulação do Mercado de Medicamentos 525418100050401
CA Health Products and Food Branch 02469723
EE Ravimiamet 1753275
ES Centro de información online de medicamentos de la AEMPS 1171214001
FI Lääkealan turvallisuus- ja kehittämiskeskus 480316
FR Base de données publique des médicaments 60199966
GB Medicines & Healthcare Products Regulatory Agency 348648
HK Department of Health Drug Office 65956
IL מִשְׂרַד הַבְּרִיאוּת 8147
JP 医薬品医療機器総合機構 4291438A1022
LT Valstybinė vaistų kontrolės tarnyba 1083944
NL Z-Index G-Standaard, PRK 148008
PL Rejestru Produktów Leczniczych 100400386
RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale W65131001
SG Health Sciences Authority 15672P
TR İlaç ve Tıbbi Cihaz Kurumu 8699808770134
US FDA, National Drug Code 44087-3535

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