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AbbVie seeks FDA OK for triple direct-acting HCV antiviral

This article was originally published in Scrip

Executive Summary

AbbVie revealed on 22 April it had submitted a new drug application (NDA) to the FDA for the company's triple direct-acting antiviral (DAA) combination regimen – ABT-450/r, a protease inhibitor and ritonavir; ombitasvir (ABT-267), a NS5A inhibitor; and dasabuvir (ABT-333), a non-nucleoside polymerase inhibitor – with or without ribavirin for patients with hepatitis C virus (HCV) genotype 1.


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