High sustained virologic response on AbbVie's Viekirax + Exviera in interim study

11 September 2015
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Interim results from an interim study of AbbVie’s (NYSE: ABBV) Viekirax (ombitasvir/paritaprevir/ritonavir) and Exviera (dasabuvir) showed a 98% sustained virologic response at 12 weeks post-treatment in chronic hepatitis C patients.

The primary endpoint of the AMBER study is the percentage of patients achieving sustained virologic response at 12 weeks post-treatment after being given the combination with or without ribavirin. This study of Polish patients who reached post-treatment at week 12 showed a 98% sustained virologic response.

Safety analysis of the interim study showed that of the 186 patients enrolled showed that adverse events were mostly mild, most commonly fatigue, nausea and headache. Serious adverse events occurred in 4% of the participants, and included hepatic decompensation, anemia and kidney insufficiency hepatotoxicity.

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