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Novo’s haemophilia drug gets EU approval

By Thomson Reuters Nov 13, 2026 | 11:27 AM

Nov 13 (Reuters) – Novo Nordisk said on Friday the European Commission has granted approval for its treatment to prevent or ​reduce the frequency of bleeding episodes ‌in adults and children with haemophilia A, a rare blood disorder.

Here are more details:

• The drug, branded Frehemgo, is a next-generation antibody designed to mimic ‌the ​activity of the blood-clotting ⁠protein called factor VIII, ⁠according to Novo. It is administered as an under-the-skin injection

• Patients with haemophilia A, with or without inhibitors, can choose between ​once-monthly, once-every-two-weeks or once-weekly dosing, Novo said

• Haemophilia is a rare genetic bleeding ⁠disorder that impairs the ⁠body’s ability to make blood clots. ​There are different types of haemophilia, with haemophilia ​A caused by a missing or defective ‌clotting factor VIII

• The approval is based on results from the clinical trial program testing the drug. In one study, Novo ⁠said the drug significantly reduced annual bleeding rates compared with prior preventive and on-demand treatments in people ⁠with hemophilia ‌A, with or without inhibitors

• ⁠Novo plans to launch Frehemgo ​in the ‌first European countries over the ​next year, ⁠it said

• The US FDA in October extended its review of the drug due to ongoing remediation work at a manufacturing facility

(Reporting by Sneha S K in Bengaluru; Editing by ​Jonathan Ananda)