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Voncento (human coagulation factor VIII / human von willebrand factor)

Region
🇪🇺 EU
Active substance
human coagulation factor VIII / human von willebrand factor
Company
CSL Behring GmbH
Status
Authorised
Therapeutic area
Hemophilia A; von Willebrand Diseases
EU approval
Mon 12 Aug 2013
Application
EMEA/H/C/002493
ATC
B02BD06
Official record
www.ema.europa.eu

Indication

Von Willebrand disease (VWD) Prophylaxis and treatment of haemorrhage or surgical bleeding in patients with VWD, when desmopressin (DDAVP) treatment alone is ineffective or contraindicated. Haemophilia A (congenital factor-VIII deficiency) Prophylaxis and treatment of bleeding in patients with haemophilia A.

Regulatory milestones

No milestones recorded in the last year.

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Information from official EMA, FDA, Federal Register and SEC records. Dates marked company-announced come from the company's own SEC filing; dates marked estimate are calculated, not official. Not investment or medical advice; always confirm on the source.