Pharmamarketeer

Novartis’ Gilenya scores paediatric EU approval for advanced relapsing-remitting MS

Novartis has announced that Gilenya (fingolimod) has received marketing authorisation from the European Commission for the treatment of relapsing-remitting forms of multiple sclerosis (RRMS) in patients aged between 10 and 17 years old, marking the availability of the first and only oral disease-modifying treatment for that age group in this indication.

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