Monoclonal antibody | |
---|---|
Type | Whole antibody |
Source | Human |
Target | TFPI |
Clinical data | |
Trade names | Hympavzi |
Other names | PF-06741086, marstacimab-hncq |
AHFS/Drugs.com | Hympavzi |
License data |
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Routes of administration | Intravenous |
Drug class | Tissue factor pathway inhibitor (TFPI) |
ATC code |
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Legal status | |
Legal status | |
Identifiers | |
CAS Number | |
DrugBank | |
UNII | |
KEGG | |
Chemical and physical data | |
Formula | C6304H9766N1678O2006S44 |
Molar mass | 142569.85 g·mol−1 |
Marstacimab, sold under the brand name Hympavzi, is a monoclonal antibody medication used for the treatment of hemophilia A and hemophilia B.[1][4][2] It is a tissue factor pathway inhibitor (TFPI) antagonist.[4] It was developed by Pfizer.[5] Marstacimab is a new type of medication that, rather than replacing a clotting factor, works by reducing the amount, and therefore, the activity of, the naturally occurring anticoagulation protein called tissue factor pathway inhibitor.[4] This increases the amount of thrombin, an enzyme that is critical in blood clotting, that is generated.[4] This is expected to reduce or prevent the frequency of bleeding episodes.[4]
The most common side effects include injection site reactions, headache, and itching (pruritis).[4]
Marstacimab was approved for medical use in the United States in October 2024,[4] and in the European Union in November 2024.[3]
Hympavzi EPAR
was invoked but never defined (see the help page).FDA PR 20241011
was invoked but never defined (see the help page).