Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Octocog alfa is a recombinant protein that functions as a replacement therapy for patients with haemophilia A. It is a full-length recombinant version of human coagulation factor VIII produced using recombinant DNA technology in mammalian cells (such as Chinese hamster ovary or baby hamster kidney cells)[2][4][8]. Octocog alfa binds to endogenous von Willebrand Factor in the circulation; once activated, it acts as a cofactor for activated Factor IX to accelerate the conversion of Factor X to its active form. This cascade leads to thrombin generation and ultimately fibrin clot formation[1][2][5]. The drug is indicated for the prevention and treatment of bleeding episodes in patients with haemophilia A (congenital factor VIII deficiency), including perioperative management[5][7]. It does not contain von Willebrand Factor itself[8].
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on octocog alfa.