Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Efraloctocog alfa is a recombinant coagulation factor VIII Fc fusion protein indicated for the treatment and prophylaxis of bleeding in patients with hemophilia A (congenital factor VIII deficiency). It consists of a single molecule of B-domain deleted recombinant human coagulation factor VIII covalently linked to the Fc domain of human immunoglobulin G1 (IgG1). This fusion protein utilizes the naturally occurring neonatal Fc receptor (FcRn) recycling pathway to delay lysosomal degradation and extend the circulating half-life of the factor VIII protein, allowing for less frequent prophylactic dosing compared to standard factor VIII products. It was developed through a collaboration between Biogen and Sobi, with Sanofi subsequently acquiring rights in several territories through its acquisition of Bioverativ.
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 efraloctocog alfa.