Blueprint Medicines announces EMA validation of type II variation marketing authorisation application for Ayvakyt (avapritinib) for the treatment of advanced systemic mastocytosis

Blueprint Medicines

3 March 2021 - Blueprint Medicines today announced that the EMA has validated the company's type II variation marketing authorisation application for Ayvakyt (avapritinib) for the treatment of advanced systemic mastocytosis. 

The European Commission has granted orphan medicinal product designation to Ayvakyt for the treatment of mastocytosis.

Read Blueprint Medicines press release

Michael Wonder

Posted by:

Michael Wonder

Posted in:

Cancer , Medicine , Europe , Dossier