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GILD > SEC Filings for GILD > Form 8-K on 13-Nov-2012All Recent SEC Filings

Show all filings for GILEAD SCIENCES INC



Regulation FD Disclosure

Item 7.01 Regulation FD Disclosure

On November 12, 2012, at the American Association for the Study of Liver Diseases Liver Meeting 2012, Bristol-Myers Squibb Company presented data from its Phase 2 study evaluating Gilead Sciences, Inc.'s sofosbuvir (also known as GS-7977) in combination with daclatasvir, an investigational NS5A inhibitor, with and without ribavirin, for 12 weeks in gentotype 1 treatment-na´ve HCV infected patients. The data showed that 96% (79 of 82) of genotype 1-treatment-na´ve HCV infected patients achieved a sustained viral response four weeks (SVR-4) after the completion of a 12 week course of treatment of sofosbuvir and daclatasvir, with or without ribavirin. Of the three patients not achieving an SVR-4, all three subsequently achieved an SVR-12.

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