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AASLD 2013: Faldaprevir Triple Therapy Effective Across Patient Subgroups

The experimental hepatitis C virus (HCV) protease inhibitor faldaprevir in combination with pegylated interferon and ribavirin was effective across a range of subgroups of patients with genotype 1 infection -- including prior relapsers and non-responders -- in the STARTVerso clinical trials program, according to research presented at the recent AASLD Liver Meeting in Washington, DC.

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FDA Approves Simeprevir (Olysio) for Chronic Hepatitis C

The U.S. Food and Drug Administration last Friday approved Janssen/Medivir's next-generation hepatitis C virus (HCV) protease inhibitor simeprevir -- to be marketed under the brand name Olysio -- as an add-on to interferon-based therapy for the treatment of people with genotype 1 chronic hepatitis C. It is not yet approved for use in interferon-free combinations.

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AbbVie All-Oral Regimen Produces 96% Cure Rate, Effective Against Both HCV 1a and 1b

A 12-week interferon-free quadruple regimen of 3 direct-acting antiviral agents plus ribavirin led to sustained virological response in 95% of previously untreated, non-cirrhotic hepatitis C patients with harder-to-treat HCV subtype 1a and 98% of those with subtype 1b, AbbVie announced this week.

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AASLD 2013: Faldaprevir All-oral Regimen Shows 100% Early Sustained Response for HCV 1a

An interferon-free regimen of faldaprevir, deleobuvir, and PPI-668 led to 4-week post-treatment sustained virological response (SVR4) in all treatment-naive patients with hard-to-treat HCV subtype 1a in an ongoing Phase 2 trial, according to a late-breaking poster presentation at the 64th AASLD Liver Meeting this month in Washington, DC.

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AASLD 2013: Black Hepatitis C Patients Do Well on Sofosbuvir Oral Regimens

Interferon-free treatment using a single daily combination pill containing sofosbuvir plus ledipasvir demonstrated potent anti-HCV activity and was generally well-tolerated in a primarily African-American inner city population with genotype 1a hepatitis C, researchers reported at the recent AASLD Liver Meeting in Washington, DC. Adding a third drug resulted in high early post-treatment response rates with shorter treatment.

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