UPLIZNA

This brand name is authorized in Austria, Estonia, Spain, France, Croatia, Ireland, Italy, Japan, Lithuania, United States

Active ingredients

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

1 Inebilizumab
UNII 74T7185BMM - INEBILIZUMAB

Inebilizumab is a monoclonal antibody that specifically binds to CD19, a cell surface antigen present on pre-B and mature B-cell lymphocytes, including plasmablasts and some plasma cells. Following cell surface binding to B lymphocytes, inebilizumab supports antibody-dependent cellular cytolysis (ADCC) and antibody-dependent cellular phagocytosis (ADCP). B cells are believed to play a central role in the pathogenesis of NMOSD. The precise mechanism by which inebilizumab exerts its therapeutic effects in NMOSD is unknown.

Read about Inebilizumab

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
UPLIZNA Solution for injection FDA, National Drug Code (US) MPI, US: SPL/PLR
UPLIZNA Concentrate for solution for infusion 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
L04AG10 L Antineoplastic and immunomodulating agents → L04 Immunosuppressants → L04A Immunosuppressants → L04AG Monoclonal antibodies
Discover more medicines within L04AG10

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): 1836547, 1881806
Country: ES Centro de información online de medicamentos de la AEMPS Identifier(s): 1211602001
Country: FR Base de données publique des médicaments Identifier(s): 60878038
Country: IT Agenzia del Farmaco Identifier(s): 050085012
Country: JP 医薬品医療機器総合機構 Identifier(s): 6399429A1026
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1094784
Country: US FDA, National Drug Code Identifier(s): 72677-551

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