Biogen and AbbVie's Zinbryta approved in EU for multiple sclerosis
The European Commission (EC) has granted marketing authorization for Zinbryta (daclizumab) to treat adults with relapsing forms of multiple sclerosis (RMS).
Zinbryta is a once-monthly, self administered, subcutaneous injection and is marketed by US firms Biogen (Nasdaq: BIIB) and AbbVie (NYSE: ABBV).
Clinical data has suggested that Zinbryta offers a valuable new option with RMS, showing that it significantly reduced relapses, 24-week confirmed disability progression and new brain lesions for up to three years compared to Biogen’s Avonex (interferon beta-1a) intramuscular injection.
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