7:48 am Johnson & Johnson’s Janssen submits snDA to FDA for OLYSIO (simeprevir) for once-daily use in combinaiton with sofosbuvir for 12 weeks for the treatment of adult patients with genotype 1 chronic hepatitis C

7:48 am Johnson & Johnson’s Janssen submits snDA to FDA for OLYSIO (simeprevir) for once-daily use in combinaiton with sofosbuvir for 12 weeks for the treatment of adult patients with genotype 1 chronic hepatitis C

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