FDA Approves Esperoct (turoctocog alfa pegol, N8-GP) for Hemophilia A

Article Link: FDA Approves Esperoct (turoctocog alfa pegol, N8-GP) for Hemophilia A

Bagsværd, Denmark, 19 February 2019 – Novo Nordisk today announced that the US Food and Drug Administration (FDA) has approved the Biologics License Application for Esperoct for the treatment of adults and children with hemophilia A.
Esperoct…

Source: FDA New Drug Approvals