Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Recombinant human coagulation factor VIII is a genetically engineered protein used to replace missing or deficient clotting factor VIII in individuals with hemophilia A. Produced using Chinese Hamster Ovary (CHO) or other mammalian cell lines via recombinant DNA technology[1][2][8], it is structurally and functionally similar to endogenous human Factor VIII. The drug acts as a cofactor for Factor IXa in the activation of Factor X in the intrinsic pathway of blood coagulation. Its primary indication is for the prevention and control of bleeding episodes in adults and children with hemophilia A[2][5][7]. Multiple brands exist based on different manufacturing processes and modifications (e.g., full-length vs B-domain deleted; PEGylated forms)[8]. It does not treat von Willebrand disease unless specifically formulated with von Willebrand Factor.
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 recombinant human coagulation factor VIII.