I’m glad I chose HUMATE-P. It worked really well for me.”
—Bekah, a person with VWD who uses HUMATE-P
In clinical studies, HUMATE-P provided reliable hemostatic control for all VWD types, including Type 3—the most severe form. HUMATE-P is proven effective in patients of all ages—from infants to adults—against multiple types of bleeds:
(344 nonsurgical
bleeds in 97 patients)
(39 urgent surgeries
in 39 patients)
Excellent: Hemostasis clinically not significantly different from normal
Good: Mildly abnormal hemostasis in terms of quantity and/or quality (e.g., slight oozing)
I’m glad I chose HUMATE-P. It worked really well for me.” —Bekah, a person with VWD who uses HUMATE-P
Individual experience may vary.
I’m glad I chose HUMATE-P. It worked really well for me.”
—Bekah, a person with VWD who uses HUMATE-P
HUMATE-P contains the VWF proteins that are important for correcting the coagulation defect in people with VWD. Several studies have shown that the composition of these VWF proteins in HUMATE-P is similar to the VWF proteins found in normal plasma.
FVIII may be missing in many people who have VWD. With insufficient FVIII activity, it can take much longer for a stable blood clot to form.
HUMATE-P provides VWF and FVIII in a 2.4 to 1 ratio.
At CSL Behring, we are dedicated to meeting the most stringent international standards for plasma product safety according to guidelines from worldwide regulatory agencies. Our Integrated Safety System helps HUMATE-P meet high quality and safety standards, thus reducing the risk of virus transmissions. The risk of virus transmission cannot be completely eliminated.