MABCAMPATH

This brand name is authorized in Canada, Japan, Turkey

Active ingredients

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

1 Alemtuzumab
UNII 3A189DH42V - ALEMTUZUMAB

Alemtuzumab is a genetically engineered humanised IgG1 kappa monoclonal antibody specific for a 21-28 kD lymphocyte cell surface glycoprotein (CD52) expressed primarily on the surface of normal and malignant peripheral blood B and T cell lymphocytes. Alemtuzumab acts through antibody-dependent cellular cytolysis and complement-mediated lysis following cell surface binding to CD52, a cell surface antigen present at high levels on T (CD3+) and B (CD19+) lymphocytes, and at lower levels on natural killer cells, monocytes, and macrophages.

Read about Alemtuzumab

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
MabCampath 30mg/ml concentrate for solution for infusion Medicines & Healthcare Products Regulatory Agency (GB) 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
L04AG06 Alemtuzumab L Antineoplastic and immunomodulating agents → L04 Immunosuppressants → L04A Immunosuppressants → L04AG Monoclonal antibodies
Discover more medicines within L04AG06

Authorization and marketing

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

Country Identification scheme Identifier(s)
Country: CA Health Products and Food Branch Identifier(s): 02290960
Country: JP 医薬品医療機器総合機構 Identifier(s): 4291428A1029
Country: TR İlaç ve Tıbbi Cihaz Kurumu Identifier(s): 8699545766643

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