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Results ION-3 and Pooled Alternatiive. by Different Patient Types 8 and 12 Weeks of HARVONI in. ION-3 and HCV-TARGET ION-3, Pooled Real-world Analysis, and HCV-TARGET Study Designs. 8 weeks of HARVONI demonstrated clinical and real-world efficacy in a broad range of GT 1 Viagrx patients 2,6. 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.

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