Authorised gene therapy Hemgenix (etranacogene dezaparvovec) for Hemophilia B with conditional approval by EMA.
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Browse all →Voranigo (vorasidenib) from Les Laboratoires Servier has been authorised by the EMA for certain gliomas, including oligodendroglioma and astrocytoma, and has orphan medicine status.
Tecvayli has been authorised by the EMA for multiple myeloma.
EMA authorised Blenrep (belantamab mafodotin) for multiple myeloma, with GSK as the marketing authorisation holder.
EMA Authorised status for Comirnaty (BioNTech) for COVID-19 infection; authorised as a vaccine with mRNA encoding the SARS-CoV-2 spike protein.
The EMA has authorised Spikevax (Moderna) for use in the EU; it is an mRNA vaccine encoding the SARS-CoV-2 spike protein for COVID-19.
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