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European Commission approves Zeposia to treat relapsing remitting multiple sclerosis.- BMS

Read time: 1 mins
Published:28th May 2020
Bristol Myers Squibb announced that the European Commission (EC) has approved Zeposia (ozanimod) for the treatment of adult patients with relapsing remitting multiple sclerosis (RRMS) with active disease as defined by clinical or imaging features. With the EC marketing authorization, Zeposia, an oral medication taken once daily, becomes the only approved sphingosine-1-phosphate (S1P) receptor modulator for RRMS patients with active disease. The approval is based on data from the SUNBEAM and RADIANCE Part B clinical trials showing that, as compared to Avonex (interferon beta-1a), Zeposia delivered powerful efficacy as measured by annualized relapse rate (ARR), as well as on the number and size of brain lesions.
Condition: Multiple Sclerosis
Type: drug

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