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March 19, 2008 09:14 PM Eastern Time 

Il Comitato europeo per i prodotti medicinali per uso umano (Committee for Medicinal Products for Human Use, CHMP) rilascia un parere favorevole per Viread® per il trattamento dell’epatite B cronica

Raggiungimento di una pietra miliare nello sviluppo di nuove terapie potenziali per il trattamento di questa malattia potenzialmente fatale

FOSTER CITY, California--(BUSINESS WIRE)--Gilead Sciences, Inc. (Nasdaq : GILD) ha annunciato oggi che il Comitato per i prodotti medicinali per uso umano (Committee for Medicinal Products for Human Use, CHMP) dell’agenzia europea per la valutazione dei farmaci (European Medicines Agency, EMEA) ha rilasciato un parere favorevole in risposta alla domanda di ampliamento delle indicazioni d’uso per Viread® (tenofovir disoproxil fumarato) per includervi il trattamento dell’epatite B cronica negli adulti. La domanda, nota come variazione di Tipo II, era stata depositata presso gli enti normativi europei competenti nell’ottobre del 2007.

Il testo originale del presente annuncio, redatto nella lingua di partenza, è la versione ufficiale che fa fede. Le traduzioni sono offerte unicamente per comodità del lettore e devono rinviare al testo in lingua originale, che è l'unico giuridicamente valido.

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Gilead Sciences, Inc.
Susan Hubbard, +1 650 522 5715 (Investitori)
Cara Miller, +1 650 522 1616 (Media)
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