European Commission approves label expansion of Roche’s Hemlibra to include people with moderate haemophilia A in the EU

Roche

1 February 2023 - The approval is based on the HAVEN 6 results, where Hemlibra demonstrated effective bleed control and a favourable safety profile in people with moderate haemophilia A without inhibitors.

Roche today announced that the European Commission approved the expansion of the Hemlibra (emicizumab) European Union marketing authorisation.

Read Roche press release

Michael Wonder

Posted by:

Michael Wonder

Posted in:

Outcome , Medicine , Europe