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Update on the HCV Antiviral Pipeline. Todd S. Wills, MD SPNS HCV Treatment Expansion Initiative Evaluation and Technical Assistance Center Infectious Disease Specialist. HCV Response Rates in HIV+ and HIV- Patients Treated With PegIFN /RBV. APRICOT HIV Positive Overall SVR: 40%. PRESCO
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Update on the HCV Antiviral Pipeline Todd S. Wills, MD SPNS HCV Treatment Expansion Initiative Evaluation and Technical Assistance Center Infectious Disease Specialist
HCV Response Rates in HIV+ and HIV- Patients Treated With PegIFN/RBV APRICOT HIV Positive Overall SVR: 40% PRESCO HIV Positive Overall SVR: 50% FRIED HIV Negative Overall SVR: 56% 100 76 80 72 62 60 46 Patients With SVR (%) 36 40 29 20 176 95 191 152 298 140 n = 0 GT1/4 GT2/3 GT1/4 GT2/3 GT1/4 GT2/3 48 Wks of Therapy,600 mg RBV 24, 48, or 72 Wks of Therapy,Weight-Based RBV 48 Wks of Therapy,Weight-Based RBV Soriano V, et al. Care of patients coinfected with HIV and hepatitis C virus: 2007 updated recommendations from the HCV–HIV International Panel AIDS. 2007;21:1073-1089.
Potential HCV antiviral targets C E1 E2/NS1 NS2 NS3 NS4A NS4B NS5A NS5B 5’ 3’ Internal ribosomal entry site RNA binding site Envelope glyco- proteins Signal peptide Serine protease/ helicase RNA dependent RNA polymerase telaprevir, boceprevir
Adherence • Triple therapy presents challenges with already busy schedules[143] • TID dosing • Food requirements • Data show pegIFN/RBV adherence decreases over time[5] • Addition of PIs may exacerbate this trend 1. Telaprevir [package insert]. May 2011. 2. Boceprevir [package insert]. May 2011. 3. EMA. Boceprevir [package insert] 2011.4. EMA. Telaprevir [package insert] 2011. 5. Lo Re V 3rd, et al. Ann Intern Med. 2011;155:353-360. from Clinical Care Options
Study 110: High Rates of Early Response With TVR + PR in Coinfected Patients • Similar efficacy results observed with or without concurrent ART • Nausea, pruritus, dizziness, fever more common with TVR vs placebo • Pharmacokinetic interactions with ATV or EFV not clinically significant Undetectable HCV RNA, Week 4 (ITT) Undetectable HCV RNA, Week 12 (ITT) No ART ATV/RTV-based ART EFV-based ART Total 100 100 75 75 71 71 80 80 70 68 64 57 60 60 Undetectable HCV RNA (%) Undetectable HCV RNA (%) 40 40 17 14 12 20 12 12 20 5 0 0 0 0 12/16 9/14 26/37 5/7 0/6 1/8 0/8 1/22 12/16 8/14 25/37 n/N = 5/7 1/6 1/8 1/8 3/22 n/N = Telaprevir + PR PR Telaprevir + PR PR Sulkowski M, et al. CROI 2011. Abstract 146LB.
Study 110 – SVR 12 Data Dieterich D, et al. CROI 2012 Abstract 46
Telaprevir plus PegINF and Ribavirin in HIV/HCV Infected Patients – Side Effects *no cases of severe rash Sherman, KE et al.. AASLD Conference November 2011 – Late Breaker Abstract 8
Boceprevir in Addition to Pegylated INF alfa 2a in HIV/HCV Patients on ARVs Sulkowski, M. CROI 2012 Abstract 47
PSI-7977 – Phase II Trial Data HCV uridine nucleotide analogue Genotype 1 Genotype 2/3 Lawritz, E. et al. J of Hepatology 54 (s1) 2012
TMC-435 – Phase IIb trial data • HCV NS3/4A Protease Inhibitor (Once-Daily) • Prior Treatment Failures 100 mg Zeuzem S., et al. J of Hepatology 54 (s1) 2012 150 mg P<0.001 vs placebo
Interferon Sparing Strategies • ABT 450/r – ritonovir boosted HCV PI + • ABT 072 – HCV polymerase inhibitor + • Weight-based ribavirin • Open label 12 week treatment trial 11 patients • Interferon sparing • 91% SVR24 • One patient relapsed 8 weeks post Rx • All patients were IL28B CC Lawitz, E. et al. Of Hepatology 56(s1) 2012
Interferon AND Ribavirin Sparing Strategies • Daclatasvir (NS5A replication complex inhibitor) + • Asunaprevir (HCV NS3 PI) • Open label trial of both drugs in 43 prior null responders or with IFN/R intolerance Suzuki, F. et al. J of Hepatology 56 (s1) 2012