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Interferon Beta-1b (Extavia) Approved in European Union for Treatment of Multiple Sclerosis BASEL, Switzerland -- May 27, 2008 -- The European Commission has approved interferon beta-1b, marketed as Extavia, for the treatment of early and relapsing forms of multiple sclerosis (MS). Formerly known as NVF233, Extavia is the same medicine as Betaferon/Betaseron, which is marketed by Bayer-Schering and was the first interferon beta treatment for MS. Novartis gained rights to its own branded version of this medicine in agreements with Bayer-Schering related to the acquisition of Chiron. Novartis also recently filed for approval of interferon beta-1b with the US Food and Drug Administration. In the EU, interferon beta-1b is approved for patients with relapsing-remitting MS and for a steadily worsening form of the disease known as secondary progressive MS with relapses. In addition, interferon beta-1b is approved to treat patients with early MS who: · Have experienced a single demyelinating event · Have an active inflammatory process that is severe enough to need treatment with intravenous corticosteroids, if alternative diagnoses have been excluded · Are at high risk of developing clinically definite MS SOURCE: Novartis AG E-mail this page to a friend or colleague! To print, use this version