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AbbVie To Present Investigational Data From Phase II Hepatitis C Program At The Liver Meeting
Date:10/1/2013

king a Triple-DAA Regimen for 12 Weeks
Poster #1096
November 3rd, 8:00AM ET; Poster Hall
This study presents medication adherence data based on electronic compilation of drug dosing history among 327 patients receiving the investigational triple-DAA regimen plus ribavirin for 8, 12 or 24 weeks.
  • Health-Related Quality of Life (HRQoL), Health State, Function and Wellbeing of Chronic HCV Patients Treated with Interferon-Free, Oral DAA Regimens: Patient Reported Outcome (PRO) Results from the AVIATOR Study
    Poster #1113
    November 3rd, 8:00AM ET; Poster Hall
    This intent-to-treat analysis from the phase IIb AVIATOR study includes patient reported outcomes (PRO) in patients receiving 12-week, ribavirin-containing investigational triple-DAA regimen.
  • Safety of Ribavirin-containing Regimens of ABT-450/r, ABT-333, and ABT-267 for the Treatment of HCV Genotype 1 Infection and Efficacy in Subjects with Ribavirin Dose Reductions
    Poster #1118
    November 3rd, 8:00AM ET; Poster Hall
    This study examined the safety of a ribavirin-containing, investigational triple-DAA, interferon-free regimen and the effects of ribavirin dose reductions on treatment response.
  • HCV RNA "Target Detected" after "Target Not Detected" During IFN-Free Treatment: Time to Worry or Not?
    Poster #1125
    November 3rd, 8:00AM ET; Poster Hall
    This study examined the frequency of TDANs (Target Detected After Not Detected) and the likelihood of subsequent virologic failure in subjects from the phase IIb AVIATOR study treated with ABT- 450/r plus ABT-267 plus ABT-333 plus ribavirin for 12 or 24 weeks in treatment naïve and null responders. 
  • Adherence to Interferon-containing Therapy Among Veteran Affairs Hepatitis C Patients
    Poster #1909
    November 5th, 8:00AM ET; Poster Hall
    Data from the United States Veterans Health Administration (VHA) Medical SAS Dataset (years 2008 to 2
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  • SOURCE AbbVie Inc.
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