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We expect adjusted EBITDA in 2016 to be approximately 219 million to 230 million, an increase of 13 to 19 in 2015. Adjusted EBITDA as a percentage of revenue is expected to be approximately 32 to 33 compared to 30 in 2015, and we expect net income in 2016 to be approximately 79 million to 89 million or 1. 75 to 1. 90 per diluted share compared to 64 million or 1. 48 per diluted share in 2015.

Clinical trial and pooled real-world analysis results in GT 1 TN adults without cirrhosis who have pre-treatment HCV RNA lt;6 million IUmL following 8 weeks of HARVONI 2,6,a-c. SVR12 in GT 1 patients in the ION-3 clinical trial and the Pooled Real-world Analysis 2,6. The pooled real-world analysis used individual patient data from the German IFI (Institut f252;r Interdisziplin228;re Medizin), Temple UniversityBurman8217;s Pharmacy, and Kaiser Permanente Southern California 2. In the ION-3 clinical trial and the pooled real-world analysis, the 8-week HARVONI option delivered high cure rates regardless of GT 1a or 1b subtype, ethnicity, or fibrosis stage 2,6.]