The World Health Organization's ATC classification organizes medical drugs based on therapeutic properties, chemical composition, and anatomy. It helps make essential medicines readily available globally and is widely used in the pharmaceutical industry.
Level | Code | Title | |
---|---|---|---|
1 | L | Antineoplastic and immunomodulating agents | |
2 | L01 | Antineoplastic agents | |
3 | L01F | Monoclonal antibodies and antibody drug conjugates | |
4 | L01FA | CD20 (Clusters of Differentiation 20) inhibitors |
Code | Title | |
---|---|---|
L01FA01 | Rituximab | |
L01FA02 | Ofatumumab | |
L01FA03 | Obinutuzumab |
Active Ingredient | Description | |
---|---|---|
Obinutuzumab |
Obinutuzumab is a recombinant monoclonal humanised and glycoengineered Type II anti-CD20 antibody of the IgG1 isotype. It specifically targets the extracellular loop of the CD20 transmembrane antigen on the surface of non-malignant and malignant pre-B and mature B-lymphocytes. Glycoengineering of the Fc part of obinutuzumab results in higher affinity for FcγRIII receptors on immune effector cells such as natural killer cells, macrophages and monocytes as compared to non-glycoengineered antibodies. |
|
Ofatumumab |
Ofatumumab is a human monoclonal antibody (IgG1) that binds specifically to a distinct epitope encompassing both the small and large extracellular loops of the CD20 molecule. The CD20 molecule is a transmembrane phosphoprotein expressed on B lymphocytes from the pre-B to mature B lymphocyte stage and on B-cell tumours. The binding of ofatumumab to the membrane-proximal epitope of the CD20 molecule induces recruitment and activation of the complement pathway at the cell surface, leading to complement dependent cytotoxicity and resultant lysis of tumour cells. |
|
Rituximab |
Rituximab binds specifically to the transmembrane antigen, CD20, a non-glycosylated phosphoprotein, located on pre-B and mature B lymphocytes. The antigen is expressed on >95% of all B cell non-Hodgkin’s lymphomas. |
Title | Information Source | Document Type | |
---|---|---|---|
ARZERRA Concentrate for solution for infusion | European Medicines Agency (EU) | MPI, EU: SmPC | |
BLITZIMA Concentrate for solution for infusion | European Medicines Agency (EU) | MPI, EU: SmPC | |
GAZYVA Solution for injection | FDA, National Drug Code (US) | MPI, US: SPL/PLR | |
GAZYVARO Concentrate for solution for infusion | European Medicines Agency (EU) | MPI, EU: SmPC | |
KESIMPTA Solution for injection | European Medicines Agency (EU) | MPI, EU: SmPC | |
REDDITUX Concentrate for solution for infusion | Health Products Regulatory Authority (ZA) | MPI, Generic | |
RITEMVIA Concentrate for solution for infusion | European Medicines Agency (EU) | MPI, EU: SmPC | |
RITUXAN Solution for injection | FDA, National Drug Code (US) | MPI, US: SPL/PLR | |
RUXIENCE Concentrate for solution for infusion | European Medicines Agency (EU) | MPI, EU: SmPC | |
TRUXIMA Concentrate for solution for infusion | European Medicines Agency (EU) | MPI, EU: SmPC |