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Medical University of Vienna — PHASE2
Hemab ApS — PHASE1, PHASE2
Hemab ApS
Vonvendi: FDA approved
For use in adults (age 18 and older) diagnosed with von Willebrand disease (VWD) for routine prophylaxis to reduce the frequency of bleeding episodes in patients with severe Type 3 VWD receiving on-demand therapy
VWD Connect Foundation
Alphanate: FDA approved
For surgical and/or invasive procedures in patients with von Willebrand Disease (VWD) in whom desmopressin is either ineffective or contraindicated. It is not indicated for patients with severe VWD (Type 3) undergoing major surgery
Humate-P: FDA approved
(1) In adult patients for treatment and prevention of bleeding in hemophilia A (classic hemophilia) and (2) in adult and pediatric patients for treatment of spontaneous and trauma-induced bleeding episodes in severe von Willebrand disease, and in mild and moderate von Willebrand disease where use of desmopressin is known or suspected to be inadequate.
Data from FDA regulatory filings and ClinicalTrials.gov. Updated periodically.
FINANCIAL LANDSCAPE SUMMARY
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Copay Assistance3
Humate-P
CSL Behring
Vonvendi
Takeda Pharmaceuticals U.S.A., Inc.
Alphanate
Grifols Biologicals Inc.
Vonvendi
(von Willebrand factor (recombinant))Orphan drugTakeda Pharmaceuticals U.S.A., Inc.
Alphanate
(Antihemophilic factor (human))Orphan drugGrifols Biologicals Inc.
Humate-P
(Antihemophilic factor/von Willebrand factor complex (human), dried, pasteurized)Orphan drugCSL Behring