|  Library 
              of Slides and Posters | 
         
          | Hepatitis 
              B | 
         
          |  | Continued 
            Effi cacy and Safety Through 4 Years of Tenofovir 
            Disoproxil Fumarate (TDF) Treatment in HBeAg-Negative Patients 
            with Chronic Hepatitis B (Study 102) P 
            Marcellin and others. AASLD 2010.
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          |  | TenofovirDisoproxilFumarate 
            (TDF) Versus EmtricitabinePlus TDF (FTC/TDF) for Treatment 
            of Chronic Hepatitis B (CHB) In Patients with Persistent Viral Replication 
            Receiving AdefovirDipivoxil: Final Week 168 Results T 
            Berg and others. AASLD 2010.
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          |  | HBV 
            rtN236T Mutant Subpopulations Respond Like Wild-Type During Tenofovir 
            DF (TDF) Monotherapy or Combination Therapy with Emtricitabine 
            (FTC): an Evaluation of Early Viral Load Decay Kinetics M 
            Curtis and others. AASLD 2010.
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          |  | Four 
            Years Efficacy and Safety of Tenofovir Disoproxil 
            Fumarate (TDF) in Asians with HBeAg-Positive and HBeAg-Negative 
            Chronic Hepatitis B E 
            Gane and others. AASLD 2010.
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          |  | 4 
            Year Efficacy of TenofovirDisoproxilFumarate 
            (TDF) in Chronic Hepatitis B Patients with High Viral Load 
            (HBV DNA .9 log10copies/mL) S 
            Gordon and others. AASLD 2010.
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          |  | Long 
            Term (4 Year) Effi cacy and Safety of Tenofovir 
            Disoproxil Fumarate (TDF) Treatment in HBeAg-Positive Patients 
            (HBeAg+) with Chronic Hepatitis B (Study 103) E 
            Healthcote and others. AASLD 2010.
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          |  | No 
            Resistance to Tenofovir Disoproxil Fumarate 
            (TDF) Detected Following up to 192 Weeks of Treatment in 
            Subjects Mono-Infected with Chronic Hepatitis B Virus A 
            Snow-Lampart and others. AASLD 2010.
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          |  | Long-term 
            Entecavir Treatment for Up to 
            5 Years in Asians With HBeAg-positive Chronic Hepatitis B: Results 
            From ETV-022 and -901 C Pan and others. AASLD 2010.
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          |  | Efficacy 
            and Safety of Entecavir in Nucleos(t)ide 
            Naïve Asians With HBeAg-Positive and -Negative Chronic Hepatitis 
            B: Results from Studies ETV-022/027 R Gish and others. AASLD 2010.
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          |  | Evaluation 
            of Amino Acid Substitutions in the Overlapping Envelope and Polymerase 
            Genes of HBV Among Treatment Naïve and Experienced Subjects Reveal 
            Significant Changes Associated with Lamivudine 
            and Adefovir, but not Tenofovir 
            DF Treatment A 
            Snow-Lampart and others. AASLD 2010.
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          | Hepatitis 
              C | 
         
          |  | Efficacy 
            and Safety of TMC435 in Combination With 
            Peginterferon a-2a and Ribavirin in Treatment-naïve 
            Genotype-1 HCV Patients: 24-Week Interim Results from the PILLAR Study M 
            Fried and others. AASLD 2010.
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          |  | In 
            vitro studies investigating the mechanism of interaction between 
            TMC435 and hepatic transporters M 
            Huisman and others. AASLD 2010.
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          |  | Virologic 
            analysis of genotype-1-infected patients treated with once-daily TMC435 
            during the Optimal Protease inhibitor Enhancement of Response to TherApy 
            (OPERA)-1 study O 
            Lenz and others. AASLD 2010.
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          |  | A 
            Phase IIa, open-label study to assess the antiviral activity of TMC435 
            monotherapy in patients infected with HCV genotypes 26 C 
            Moreno and others. AASLD 2010.
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          |  | Pharmacokinetic-pharmacodynamic 
            analyses of TMC435 in patients 
            infected with hepatitis C virus genotypes 26 V 
            Sekar and others. AASLD 2010.
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          |  | 4-Week 
            Virologic Response and Safety of ABT-450 
            Given with Low-dose Ritonavir (ABT-450/r) First As 3-Day Monotherapy 
            Then in Combination with Pegylated Interferon Alpha-2a and Ribavirin 
            (SOC) in Genotype 1 (GT1) HCV-infected Treatment-naïve Subjects E 
            Lawitz and others. AASLD 2010.
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          |  | Initial 
            Antiviral Activity of the HCV NS3 Protease Inhibitor ABT-450 
            When Given with Low-dose Ritonavir as 3-Day Monotherapy: Preliminary 
            Results of Study M11-602 in Genotype 1 (GT1) HCV-infected Treatment-naïve 
            Subjects E 
            Lawitz and others. AASLD 2010.
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          |  | HCV 
            RESPOND-2 Final Results High Sustained Virologic Response Among Genotype 
            1 Previous Non-Responders and Relapsers to Peginterferon/Ribavirin 
            when Re- Treated with Boceprevir Plus PEGINTRON 
            (Peginterferon alfa-2b)/Ribavirin B 
            Bacon and others. AASLD 2010.
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          |  | Boceprevir 
            Combined with Peginterferon alfa-2b/Ribavirin for Treatment-Naïve 
            Patients with HCV Genotype 1 F 
            Poordad and others. AASLD 2010.
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          |  | Frequencies 
            of Resistance-Associated Amino Acid Variants Following Combination 
            Treatment with Boceprevir Plus PEGINTRON 
            (PegInterferon Alfa-2b)/Ribavirin in Patients With Chronic 
            Hepatitis C (CHC), Genotype 1 (G1) J 
            Vierling and others. AASLD 2010.
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          |  | Hemoglobin 
            Decline During Lead-in Phase as an Early Predictor of Anemia After 
            the Addition of Boceprevir: A 
            Retrospective Analysis of HCV SPRINT-1 F 
            Poordad and others. AASLD 2010.
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          |  | Response-Guided 
            Therapy with Boceprevir + Peginterferon alfa-2b/Ribavirin 
            for Treatment-Naïve Patients with Hepatitis C Virus Genotype 
            1 Was Similar to a 48-Wk Fixed-Duration Regimen with Boceprevir + 
            Peginterferon alfa-2b/Ribavirin in SPRINT-2 J 
            Bronowicki and others. AASLD 2010.
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          |  | Strong 
            antiviral activity and safety of IFN-sparing treatment with the protease 
            inhibitor BI 201335, the HCV polymerase 
            inhibitor BI 207127, and ribavirin, in patients 
            with chronic hepatitis C: the SOUND-C1 trial S Zeuzem and others. AASLD 2010.
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          |  | Virological 
            response and safety of 4 weeks treatment with the protease 
            inhibitor BI 201335 combined with 48 weeks of 
            peginterferon alfa 2a and ribavirin 
            for treatment of HCV GT-1 patients who failed peginterferon/ribavirin T Berg and others. AASLD 2010.
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          |  | Genotypic 
            and phenotypic analysis of the NS5B polymerase region from viral isolates 
            of HCV chronically infected patients treated with BI 
            207127 for 5 days monotherapy L Lagace, and others. AASLD 2010.
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          |  | BMS-790052, 
            a First-in-Class Potent Hepatitis C Virus NS5A Inhibitor, Demonstrates 
            Multiple-Dose Proof-of-Concept in Subjects With Chronic GT1 HCV Infection R Nettles and others. AASLD 2010.
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          |  | Coadministration 
            of BMS-790052 and BMS-650032 Does 
            Not Result in a Clinically Meaningful Pharmacokinetic Interaction 
            in Healthy Subjects M Bifano and others. AASLD 2010.
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          |  | Pipeline 
            Asset Update for BMS-790052 (NS5A inhibitor) 
            and BMS-650032 (NS3 
            inhibitor) Btistol-Myers Squibb Company. AASLD 2010.
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          |  | Combination 
            Therapy With BMS-790052 and BMS-650032 Alone 
            or With Pegylated Interferon and Ribavirin (pegIFN/RBV) 
            Results in Undetectable HCV RNA Through 12 Weeks of Therapy in HCV 
            Genotype 1 Null Responders A Lok and others. AASLD 2010.
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          |  | BMS-824393 
            Is a Potent Hepatitis C Virus NS5A Inhibitor With Substantial Antiviral 
            Activity When Given as Monotherapy in Subjects With Chronic G1 HCV 
            Infection R Nettles and others. AASLD 2010.
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          |  | Safety 
            and Antiviral Activity of MK-5172, 
            a Novel HCV NS3/4a Protease Inhibitor with Potent Activity Against 
            Known Resistance Mutants, in Genotype 1 and 3 HCV-Infected Patients A 
            Petry and others. AASLD 2010.
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          |  | Safety, 
            Tolerability, and Pharmacokinetics after Single and Multiple Doses 
            of MK-5172, a Novel HCV NS3/4a 
            Protease Inhibitor with Potent Activity Against Known Resistance Mutants, 
            in Healthy Subjects A 
            Petry and others. AASLD 2010.
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          |  | High 
            Correlation Between Week 4 and Week 12 as the Definition for Null 
            Response to Peginterferon alfa (PEG) Plus 
            Ribavirin (R) Therapy: Results From the IDEAL Trial F 
            Poordad and others. AASLD 2010.
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          |  | Impact 
            of PegIntron (PEG) Maintenance 
            Therapy (MT) on Fibrosis Biomarkers (FibroTest [FT]/FibroSURE) in 
            Prior Nonresponders With METAVIR Fibrosis Scores (MFS) of F2/F3: Final 
            Results From the EPIC3 Program T 
            Poynard and others. AASLD 2010.
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          |  | The 
            Effect of Treatment Group, HCV Genotype, and IL28B Genotype on Early 
            HCV Viral Kinetics in a Phase 2a Study of PEG-Interferon 
            Lambda (pegIFNë) in Hepatitis C Patients J Freeman and others. AASLD 2010.
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          |  | Pegylated 
            Interferon Lambda (pegIFNë) Phase 2 Dose-Ranging, 
            Active-Controlled Study in Combination With Ribavirin 
            (RBV) for Treatment-Naive HCV Patients (Genotypes 1, 2, 
            3, or 4): Safety, Viral Response, and Impact of IL28B Host Genotype 
            Through Week 12 A Muir and others. AASLD 2010.
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          |  | Pharmacokinetics 
            of PEG-Interferon Lambda (pegIFNë) 
            Following Fixed Dosing in Treatment-Naive Hepatitis C Subjects (Single-Dose 
            Interim Data From a Dose-Ranging Phase 2a Study) K Byrnes-Blake and others. AASLD 2010.
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          |  | Sustained 
            Viral Response (SVR) Rates in Genotype 1 Treatment-naïve Patients 
            with Chronic Hepatitis C (CHC) Infection Treated with Vaniprevir 
            (MK-7009), a NS3/4a Protease Inhibitor, in Combination 
            with Pegylated Interferon Alfa-2a and Ribavirin 
            for 28 Days M 
            Manns and others. AASLD 2010.
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          |  | Genotypic 
            and Phenotypic Analysis of HCV NS5A Inhibitor 
            Resistance Variants: Correlations Between In Vitro and 
            In Vivo Observations M Gao and others. AASLD 2010.
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          |  | Impaired 
            Fasting Glucose Is Associated With Lower Rates of Sustained Virologic 
            Response (SVR) in Patients With Genotype 1 Chronic Hepatitis C (CHC): 
            Retrospective Analysis of the IDEAL Study M 
            Sulkowski and others. AASLD 2010.
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          |  | Analysis 
            of Site Performance in Academic and Community-Based Centers in the 
             IDEAL Study J 
            Jou and others. AASLD 2010.
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          |  | Baseline, 
            Donor, and On-treatment Predictors of Sustained Virologic Response 
            in Patients Treated for Recurrent Hepatitis C Following Orthotopic 
            Liver Transplant: Subanalysis of the PROTECT 
            Study F 
            Gordon and others. AASLD 2010.
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          |  | Chronic 
            Hepatitis C (HCV) Infections and the Risk 
            of Depression and Other Adverse Events J McCombs and others. AASLD 2010.
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          |  | Sensitive 
            Detection of Y448H NS5B Mutant Viruses 
            in Patients Infected with Genotype 1a and 1b HCV A 
            Bae and others. AASLD 2010.
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          |  | Safety, 
            Pharmacokinetics, and Antiviral Activity of Single Oral Doses of the 
            HCV NS3 Protease Inhibitor GS-9256 R 
            Goldwater and others. AASLD 2010.
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          |  | Enhanced 
            in Vitro Antiviral Activity and Suppression of Resistance by Combining 
            GS-9256, A Novel Protease Inhibitor, 
            With GS-9190, a Non-Nucleoside 
            NS5B Inhibitor H 
            Mo and others. AASLD 2010.
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          |  | Antiviral 
            Response and Resistance Analysis of Treatment-Naïve HCV Infected 
            Subjects Receiving Single and Multiple Doses of GS-9190 J 
            Harris and others. AASLD 2010.
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          |  | Nonclinical 
            Profi le and Phase I Results in Healthy Volunteers of the Novel and 
            Potent HCV NS5A Inhibitor GS-5885 J 
            Link and others. AASLD 2010.
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          |  | Characterization 
            of HCV Resistance from Single and Multiple Dose Clinical Trials of 
            GS-9256, a Novel NS3 Protease Inhibitor K 
            Wong and others. AASLD 2010.
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          |  | Three-Day, 
            Dose-Ranging Study Of The HCV NS3 Protease Inhibitor 
            GS-9451 E 
            Lawitz and others. AASLD 2010.
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          |  | Dual, 
            Triple, and Quadruple Combination Treatment with a Protease 
            Inhibitor (GS-9256) and a Polymerase Inhibitor (GS-9190) 
            alone and in Combination with Ribavirin(RBV) or PegIFN/RBV for up 
            to 28 days in Treatment Naïve, Genotype 1 HCV Subjects S 
            Zeuzem and others. AASLD 2010.
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