EU approves VPRIV

August 27, 2010

THE European Union has approved marketing authorisation for Shire plc’s new a human cell line derived enzyme replacement therapy treatment VPRIV(R) (velaglucerase alfa). Indicated for treatment of type 1 Gaucher disease VPRIV(R) will soon be available in 30 European countries. “Gaucher disease is a rare and often debilitating condition,” said Professor Tim Cox from the Department of Medicine, University of Cambridge. “The European approval of VPRIV is important in that we now have an alternative, licensed therapeutic enzyme. “For type 1 patients the availability of VPRIV provides further opportunities to individualise treatment options for this complex disorder,” Cox added.

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Pharmacy Daily | EU approves VPRIV

EU approves VPRIV

Other recent headlines

WA group stocks vapes

Fujitsu to protect against cyber threats

PD breaking news – Queensland pharmacies scope of practice pilot expanded

SEARCH PHARMACY DAILY

Featured video

Recent issues

INDUSTRY JOB VACANCIES