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The Food and Drug Administration (FDA) recently approved AbbVie’s Mavyret, the newest treatment for chronic hepatitis C.
Mavyret taken for eight weeks was well tolerated and cured all HIV-positive people without cirrhosis in a recent study
Maviret and Vosevi were highly effective and well tolerated in clinical trials.
Glecaprevir/pibrentasvir (G/P) cured high rates of those with genotype 1 who failed a previous hep C cure attempt in a Phase II study.
The single-pill regimen would provide an eight-week ribavirin-free option for those with all viral genotypes who do not have cirrhosis.
The once-daily investigational hepatitis C virus (HCV) combination tablet will likely be approved in 2017.
AbbVie’s investigational hepatitis C virus (HCV) treatment is poised for approval in 2017.
The investigational glecaprevir/pibrentasvir performed very well among the historically hard-to-treat group, including those with cirrhosis.
AbbVie’s investigational daily, fixed-dose combination tablet performed very well among those with milder liver damage.
The FDA grants breakthrough therapy designation to AbbVie’s experimental hepatitis C regimen glecaprevir/pibrentasvir
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