Difference between revisions of "Crizanlizumab (Adakveo)"
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==History of changes in FDA indication== | ==History of changes in FDA indication== | ||
| − | *11/15/2019: Approved to reduce the frequency of vaso-occlusive crises (VOCs) in adults and pediatric patients aged 16 years and older with [[Sickle cell anemia|sickle cell disease]]. | + | *11/15/2019: Approved to reduce the frequency of vaso-occlusive crises (VOCs) in adults and pediatric patients aged 16 years and older with [[Sickle cell anemia|sickle cell disease]]. ''(Based on SUSTAIN)'' |
==Also known as== | ==Also known as== | ||
Revision as of 02:42, 11 June 2022
Mechanism of action
Definition from the NCI Drug Dictionary: A humanized monoclonal immunoglobulin G1 anti-P-selectin antibody with vaso-protective and anti-vaso-occlusive properties. Upon administration, crizanlizumab binds to P-selectin and blocks its interaction with P-selectin glycoprotein ligand-1 (PSGL-1; SELPLG) on neutrophils and monocytes. P-selectin, a glycoprotein that functions as a cell adhesion molecule (CAM), translocates to the surface of activated endothelial cells and platelets, upon stimulation, where it binds to its ligand and mediates the rolling of platelets and neutrophils on activated endothelial cells.
Diseases for which it is used
History of changes in FDA indication
- 11/15/2019: Approved to reduce the frequency of vaso-occlusive crises (VOCs) in adults and pediatric patients aged 16 years and older with sickle cell disease. (Based on SUSTAIN)
Also known as
- Code name: SEG101
- Generic name: crizanlizumab-tmca
- Brand name: Adakveo