Drug intelligence / Profile preview

turoctocog alfa

Development stage
Approved
Lead developer
Novo Nordisk
Modality
Recombinant Proteins and Enzymes
Administration
Intravenous
01

Overview

Turoctocog alfa is a recombinant, B-domain truncated human coagulation factor VIII used for the treatment and prophylaxis of bleeding in patients with hemophilia A (congenital factor VIII deficiency). It is produced using Chinese hamster ovary (CHO) cells and does not contain any human or animal proteins. The drug functions by replacing deficient or defective endogenous factor VIII in hemophilia A patients, thereby restoring the intrinsic pathway of blood coagulation. Upon activation by thrombin, the truncated B-domain is cleaved off, resulting in an active FVIII molecule that closely resembles endogenous FVIIIa. Turoctocog alfa binds to von Willebrand Factor (vWF) in circulation; once activated, it acts as a cofactor for activated factor IX to accelerate conversion of factor X to Xa—ultimately leading to thrombin generation and fibrin clot formation. Clinical trials have demonstrated its efficacy for both on-demand treatment and prophylaxis of bleeding episodes as well as perioperative management[1][4][5][8].

Brand names
NovoEight
Other names
recombinant factor VIIIrFVIIIB-domain truncated recombinant factor VIII
02

Targets

F2 (Thrombin)Coagulation Factor IXaF10 (Factor Xa)F8 (Coagulation Factor VIIIa)BB-031 (Von Willebrand factor)

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