This brand name is authorized in United States. It is also authorized in Austria, Estonia, Lithuania.
The drug LYNOZYFIC contains one active pharmaceutical ingredient (API):
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UNII
M3CPC50MZS - LINVOSELTAMAB
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Linvoseltamab is a human IgG4-based bispecific antibody that binds to cluster of differentiation 3 (CD3), a T-cell antigen associated with the T-cell receptor complex, and B-cell maturation antigen (BCMA), which is expressed on the surface of malignant multiple myeloma B-lineage cells, as well as late-stage B cells and plasma cells. Simultaneous engagement of both arms of linvoseltamab results in formation of a synapse between the T-cell and the BCMA-expressing cell, resulting in T-cell activation and generation of polyclonal cytotoxic T-cell response, which result in redirected lysis of the targeted cells, including malignant multiple myeloma B-lineage cells. |
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Below package inserts are available for further reading:
| Document | Type | Information Source | |
|---|---|---|---|
| LYNOZYFIC Concentrate for solution for infusion | MPI, EU: SmPC | European Medicines Agency (EU) |
This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
| ATC Group | Classification | |
|---|---|---|
| L01FX37 | L Antineoplastic and immunomodulating agents → L01 Antineoplastic agents → L01F Monoclonal antibodies and antibody drug conjugates → L01FX Other monoclonal antibodies | |
This drug has been assigned below unique identifiers within the countries it is being marketed:
| Country | Identification scheme | Identifier(s) |
|---|---|---|
| EE | Ravimiamet | 3133998, 3134001 |
| LT | Valstybinė vaistų kontrolės tarnyba | 1103433, 1103434 |
| US | FDA, National Drug Code | 61755-054 |
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