NULOJIX

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

Active ingredients

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

1 Belatacept
UNII E3B2GI648A - BELATACEPT

Belatacept, a modified form of CTLA4-Ig, binds CD80 and CD86 more avidly than the parent CTLA4-Ig molecule from which it is derived. This increased avidity provides a level of immunosuppression that is necessary for preventing immune-mediated allograft failure and dysfunction. Belatacept blocks CD28 mediated co-stimulation of T cells inhibiting their activation.

Read about Belatacept

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
NULOJIX Powder for 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
L04AA28 L Antineoplastic and immunomodulating agents → L04 Immunosuppressants → L04A Immunosuppressants → L04AA Selective immunosuppressants
Discover more medicines within L04AA28

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): 1533215, 1533226
Country: ES Centro de información online de medicamentos de la AEMPS Identifier(s): 11694002
Country: FR Base de données publique des médicaments Identifier(s): 69597619
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 194635, 194636
Country: IT Agenzia del Farmaco Identifier(s): 041282017, 041282029
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1061230, 1061231
Country: NL Z-Index G-Standaard, PRK Identifier(s): 101044
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100247950
Country: US FDA, National Drug Code Identifier(s): 0003-0371

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