Drug intelligence / Profile preview

octocog alfa (Takeda)

Development stage
Unknown
Lead developer
Baxter Healthcare Corporation
Modality
Recombinant Proteins and Enzymes
Administration
Intravenous
01

Overview

Recombinant antihemophilic factor (Factor VIII) is a purified glycoprotein produced by recombinant DNA technology, used for the treatment and prophylaxis of bleeding in patients with hemophilia A (congenital factor VIII deficiency). It serves as a direct replacement for the missing or deficient endogenous coagulation factor VIII. In the blood, Factor VIII acts as an essential cofactor for activated Factor IX (FIXa); together with calcium and phospholipids, they form the 'tenase' complex, which proteolytically activates Factor X to Factor Xa. This activation is a critical step in the intrinsic pathway of the coagulation cascade, leading to the generation of thrombin and the subsequent formation of a stable fibrin clot. Modern recombinant versions, such as octocog alfa (Advate), are often manufactured using protein-free methods (PFM) to eliminate the risk of pathogen transmission from human or animal-derived additives. The drug is typically administered via intravenous injection.

Brand names
AdvateKogenate FSHelixate FSRecombinateKovaltryNovoeightXynthaNuwiqAfstyla
Other names
recombinant antihemophilic factorrecombinant human coagulation factor VIIIantihemophilic factor (recombinant)moroctocog alfaturoctocog alfasimoctocog alfalonoctocog alfasusoctocog alfa
02

Targets

PS (Phosphatidylserine)F10 (Factor Xa)BB-031 (Von Willebrand factor)Coagulation Factor IXa

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