Target intelligence / Profile preview

Von Willebrand Factor (None)

Target
None
Molecular classification
Glycoprotein, Multimeric protein, Adhesion molecule, Coagulation factor regulator
01

Overview

Von Willebrand factor (VWF) is a large, multimeric glycoprotein found in blood plasma. It plays a central role in hemostasis by mediating platelet adhesion to sites of vascular injury and stabilizing coagulation factor VIII, which is essential for proper blood clotting. Deficiency or dysfunction of VWF leads to von Willebrand disease (VWD), characterized by impaired blood clotting and increased bleeding tendency.

02

Mechanism of action

Replacement therapy; promoting platelet adhesion and factor VIII stability

03

Biological functions

Platelet adhesionFactor VIII carrierHemostasisAngiogenesis
04

Disease associations

Von Willebrand diseaseHemophilia A (secondary deficiency)Vascular malformations
05

Safety considerations

Thrombotic events (rare)Anaphylactic reactionsTransmission of infectious agents (plasma-derived products)
06

Interacting drugs

Therapeutic human plasma-derived VWF

1 more in the full profile.

07

Biomarkers

VWF antigen levelsVWF activity assays (e.g., ristocetin cofactor activity)

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