Meet factor VIII, a protein that is involved in one of the steps of the blood coagulating process. Factor VIII becomes factor VIIIa when an injury happens.
Blood coagulation process continues normally
Factor VIIIa brings 2 other proteins (factor IXa and factor X) together, allowing the blood coagulation process to continue, stopping a bleed.
Blood coagulation process can’t continue normally
In people with hemophilia A who have low or missing factor VIII, the blood coagulation process cannot continue normally.
Blood coagulation process continues
HEMLIBRA acts like a bridge, bringing factor IXa and factor X together to allow the blood coagulation process to continue without needing to replace factor VIII.
Laboratory studies show that when both factor VIIIa and HEMLIBRA are available, factor VIIIa binds to factors IXa and X more readily and tightly than HEMLIBRA.
Therefore, based on laboratory studies, overcoagulation was not observed when HEMLIBRA and factor VIII were present.
Find out about HEMLIBRA studies for people with and without inhibitors.
Your local ACM is part of your hemophilia community and is an expert on HEMLIBRA. ACMs are Genentech employees and do not provide medical advice. Talk to your doctor about your treatment options.
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