ELREXFIO

This brand name is authorized in Austria, Estonia, France, Croatia, Lithuania, Romania, United States

Active ingredients

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

1 Elranatamab
UNII L0HR9A577V - ELRANATAMAB

Elranatamab is a bi-specific T-cell engaging antibody that binds CD3-epsilon on T-cells and B-cell maturation antigen (BCMA) on plasma cells, plasmablasts, and multiple myeloma cells. Binding of elranatamab to BCMA on tumour cells and CD3 on T-cells is independent of native T-cell receptor (TCR) specificity or reliance on major histocompatibility (MHC) Class 1 molecules. Elranatamab activated T-cells, led to proinflammatory cytokine release, and resulted in multiple myeloma cell lysis.

Read about Elranatamab

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
ELREXFIO Solution for injection European Medicines Agency (EU) MPI, EU: SmPC
ELREXFIO Solution for injection FDA, National Drug Code (US) MPI, US: SPL/PLR

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): 3062933, 3062944
Country: FR Base de données publique des médicaments Identifier(s): 65312065
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1098434, 1098435
Country: RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale Identifier(s): W70072001, W70072002
Country: US FDA, National Drug Code Identifier(s): 0069-2522, 0069-4494, 63539-252

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