Biogen and AbbVie's Zinbryta approved in EU for multiple sclerosis

6 July 2016

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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