Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This entry refers to a specific group of Factor VIII (FVIII) replacement therapies—Kogenate FS, Advate, Humate-P, Recombinate, and Helixate FS—that were utilized as interchangeable interventions in a clinical trial protocol sponsored by The Hospital for Sick Children (SickKids). The study, titled Pilot Study of Once-A-Day Prophylaxis for Youth and Young Adults With Severe Hemophilia A (NCT00108719), evaluated the feasibility of a once-daily low-dose prophylaxis regimen (250 or 500 units per day) using the patient's usual FVIII preparation. Most of these products (Kogenate FS, Advate, Recombinate, and Helixate FS) are recombinant forms of Factor VIII (octocog alfa), while Humate-P is a plasma-derived concentrate containing both Factor VIII and von Willebrand Factor (VWF). These agents work by replacing the deficient or absent clotting factor VIII in patients with Hemophilia A, thereby restoring the intrinsic pathway of the coagulation cascade and preventing spontaneous or traumatic bleeding episodes.
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 Kogenate FS + Advate + Humate-P + Recombinate + Helixate FS.