Merck Receives European Approval to Expand Use of Rebif in Patients with Early Multiple Sclerosis
“We are delighted by the European Commission decision,” said Dr Annalisa Jenkins, Head of Global Drug Development and Medical at the Merck Serono division. “Multiple sclerosis has an initial stage when clinical manifestations are not pronounced but irreversible neurological damage is taking place. Throughout the European Union, neurologists will now be able to prescribe Rebif for patients with early signs of this devastating disease.”
The new labelling for Rebif is valid immediately in all 27 member states of the
European Union.
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