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Data presented today show that TECFIDERA® (dimethyl fumarate)
continues to offer consistent and strong efficacy combined with a
favorable safety profile in a broad range of patients with
relapsing-remitting multiple sclerosis (RRMS), including those patients
who are newly diagnosed with the disease. These data were presented by Biogen
Idec
BIIB at the 29th Congress of the European
Committee for Treatment and Research in Multiple Sclerosis (ECTRIMS) in
Copenhagen, Denmark from 2-5 October.
Interim analyses from the ENDORSE long-term extension study show that
TECFIDERA maintained its effect in reducing disease activity in patients
treated for four years. No new or worsening safety signals were observed
in patients who had received TECFIDERA for up to six
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