Loading ...
Sorry, an error occurred while loading the content.

Fw: NATAP: AASLD Liver Meeting 2006 Reports/Coverage

Expand Messages
  • alleypat
    ... 57th Annual Meeting of the American Association for the Study of Liver Diseases (AASLD) October 27-31, 2006 Boston, MA Â Â â?¢ In Vitro Synergistic
    Message 1 of 1 , Dec 23, 2006
    • 0 Attachment
      _______________________________________________



      --------------------------------------------------------------------------------


      57th Annual Meeting of the American Association
      for the Study of Liver Diseases
      (AASLD)
      October 27-31, 2006
      Boston, MA
      Â
      Â
      â?¢ In Vitro Synergistic Antiviral Activity of ITMN-191, an Orally Active Inhibitor of the Hepatitis C Virus (HCV) NS3/4A Protease, in Combination with PEG-Interferon Alfa-2a - (11/14/06)
      Â
      â?¢ Development of HCC in Patients who Achieve SVR to IFN-Based Therapies is Associated with Cirrhosis and Prior HBV Exposure - (11/14/06)
      Â
      â?¢ CPG10101 HCV Toll-Receptor 9 Antagonist Phase II Study results - (11/10/06)
      Â
      â?¢ New HBV Drug PMEO-DAPym Active In Vitro Against Drug Resistant Mutants of HBV - (11/10/06)
      Â
      â?¢ In Vitro Resistance Studies of AG-021541, a Novel Nonnucleoside Inhibitor of the Hepatitis C Virus RNA-dependent RNA Polymerase - (11/08/06)
      Â
      â?¢ No Novel Adefovir Mutations - (11/08/06)
      Â
      â?¢ Pegasys/RBV Prophylaxisly Administered After Liver Transplant - (11/08/06)
      Â
      â?¢ RBV Exposure During weeks 1-12 of Treatment Improves SVR Rate in Canadian Pegasys EAP - (11/08/06)
      Â
      â?¢ Early predictors of anemia in patients with HCV genotype 1 treated with peginterferon alfa-2a (40KD) plus ribavirin 1000-1200 mg/day - (11/08/06)
      Â
      â?¢ PegIntron/RBV Effective for >65 Year Olds - (11/08/06)
      Â
      â?¢ New Therapy Significantly Increases Platelet Count - (11/08/06)
      Â
      â?¢ Eltrombopag, an Oral Platelet Growth Factor, Facilitates Initiation of Interferon Therapy in Subjects with HCV Associated Thrombocytopenia - (11/08/06)
      Â
      â?¢ Merck HCV Polymerase Inhibitor - (11/08/06)
      Â
      â?¢ In Vitro Resistance Studies of AG-021541, a Novel Nonnucleoside Inhibitor of the Hepatitis C Virus RNA-dependent RNA Polymerase - (11/08/06)
      Â
      â?¢ Pegasys + Adefovir Reduces HBsAg in HDV-Coinfected - (11/07/06)
      Â
      â?¢ Pegasys+Lamivudine for HBeAg-negative, 2 Year Follow-up - (11/07/06)
      Â
      â?¢ Pegasys 270 ug/wk+RBV 1200/1600mg in Difficult To Treat Patients - (11/07/06)
      Â
      â?¢ Pegasys Every 5 Days in PegIntron Nonresponders - (11/07/06)
      Â
      â?¢ Hispanic Responses to PegIntron/RBV in WIN-R Study - (11/07/06)
      Â
      â?¢ LATINO Pegasys Study: early responses - (11/07/06)
      Â
      â?¢ Anti-HBV Activity of In Vitro Combinations of Tenofovir with Nucleoside Analogs - (11/06/06)
      Â
      â?¢ In Vitro Susceptibility of HBV Polymerase Encoding Mutations Acquired During Adefovir Dipivoxil Therapy to Other Anti-HBV Agents - (11/06/06)
      Â
      â?¢ Adefovir 3 & 5 Years Followup HBeAg+: safety & efficacy - (11/06/06)
      Â
      â?¢ 16 vs 24 weeks Pegasys/RBV for Genotype 2 HCV; Taiwan Study: Week 4 Response & Ribavirin Level/Dose Predicts SVR - (11/06/06)
      Â
      â?¢ <400,000 is New HCV RNA Cutoff In genotype 1 with Pegasys/RBV - (11/06/06)
      Â
      â?¢ 72 Weeks Pegasys/RBV in Genotype 1 Improves SVR Rate For Patients With Early Viral Response (2 log reduction at wk 12) But HCV RNA >50 IU/mL - (11/06/06)
      Â
      â?¢ 72 Weeks Peg/RBV for 'Slow-Responders' Improves SVR Rate - (11/06/06)
      Â
      â?¢ 400,000 IU/ml was the best cut-off level between Low VL and High VL - (11/06/06)
      Â
      â?¢ The cyclophilin inhibitor DEBIO-025 has a potent dual anti-HIV and anti-HCV activity in treatment-naive HIV/HCV co-infected subjects - (11/03/06)
      Â
      â?¢ Entecavir vs Adefovir in HBeAg+ Naives 24 Weeks EARLY Study - (11/03/06)
      Â
      â?¢ Ribavirin Dose/Levels Predicts Outcome in Pegasys/RBV ACCELERATE Study Comparing 16 vs 24 Weeks Therapy - (11/03/06)
      Â
      â?¢ Week 4 Response Predicts SVR in Pegasys/RBV 16 Week Therapy Study in Genotypes 2/3 - (11/03/06)
      Â
      â?¢ Weight-Based Ribavirin Improves SVR Rate for Patients >125 kg (275 lbs) - (11/02/06)
      Â
      â?¢ Infergen (Consensus Interferon) Phase III DIRECT Study End of Treatment Results - (11/02/06)
      Â
      â?¢ Current status of Subjects Receiving Pegays and Ribavirin Follow-On Therapy After 28 Days Treatment with the Hepatitis C Protease Inhibitor Telaprevir (VX-950), Pegasys & RBV - (11/02/06)
      Â
      â?¢ Win-R Study: Ribavirin Weight-Base Dosing in High Weight Patients; Treatment Responses to PegIntron/RBV for Elderly Patients and by Patient Ethnicity - (11/02/06)
      Â
      â?¢ Entecavir Resistance 3-Year Update at AASLD - (11/02/06)
      Â
      â?¢ Entecavir 3-Year Resistance Update - (11/02/06)
      Â
      â?¢ Entecavir 3-Year Efficacy/Safety Update in HBeAg+ Naives - (11/02/06)
      Â
      â?¢ Entecavir 3-Year Update on Efficacy & Safety - (11/02/06)
      Â
      â?¢ Two-Year Results from the GLOBE Trial in Patients with Hepatitis B: Greater Clinical and Antiviral Efficacy for Telbivudine (LdT) vs Lamivudine - (11/01/06)
      Â
      â?¢ VX-950 HCV Protease Inhibitor Resistance Profile: combination therapy suppresses drug resistance - (11/01/06)
      Â
      â?¢ New Drug Lowers AST/ALT Levels in Chronic HCV - (11/01/06)
      Â
      â?¢ Albuferon Phase 2 Study Results Reported in Posters at AASLD - (11/01/06)
      Â
      â?¢ Albuferon Quality-Of-Life Reported - (11/01/06)
      Â
      â?¢ Roche HCV Polymerase Inhibitor Shows Potency: 4 log viral load reduction - (10/31/06)
      Â
      â?¢ Valopicitabine (NM283) plus Peg-Interferon in Treatment-Naive Hepatitis C Patients with HCV Genotype-1 Infection: HCV RNA Clearance During 24 Weeks of Treatment - (10/31/06)
      Â
      â?¢ SELECTION AND CHARACTERIZATION OF HEPATITIS C VIRUS REPLICONS RESISTANT TO A POTENT POLYMERASE INHIBITOR A-837093 - (10/30/06)
      Â
      â?¢ In vitro antiviral effects of combinations of Abbott HCV polymerase inhibitors with IFN or NS3/4A protease inhibitors - (10/30/06)
      Â
      â?¢ The Antiviral Efficacy of an HCV Polymerase inhibitor in the Chimpanzee Model: Genotypic and Phenotypic Analysis - (10/30/06)
      Â
      â?¢ Coffee Appears to Reduce Risk of Fibrosis in HCV+ - (10/30/06)
      Â
      â?¢ Daily Cannabis Use by HCV+ Increased Odds of Moderate to Severe Fibrosis by 7- Fold - (10/30/06)
      Â
      â?¢ Higher Fixed Dosing with PEGASYS in Difficult-to-Treat Patients - (10/30/06)
      Â
      â?¢ Early Week 4 Response Predicts SVR in Genotype 1 - (10/30/06)
      Â
      â?¢ Roche's Oral Polymerase Inhibitor R1626 Shows Strong Antiviral Activity in Chronic Hepatitis C Patients - (10/30/06)
      Â
      â?¢ Update on NM283, HCV Polymerase Inhibitor, at New 200 mg Dose - (10/30/06)

      â?¢ New Data for Investigational Hepatitis C Drug Telaprevir (VX-950) to be Presented at AASLD Meeting - (10/30/06)
      Â
      â?¢ Valeant Pharmaceuticals Previews 24-Week Results of Direct Trial for Infergen (Consensus Interferon) - (10/30/06)
      Â


      Â




      --------------------------------------------------------------------------------


      _______________________________________________
      NATAP nataphcv mailing list -- nataphcv@...

      This is an annoucement-only mailing list. Do not reply.

      To unsubscribe: send a blank email to nataphcv-request@... with a subject of unsubscribe.


      For more information, see http://seven.pairlist.net/mailman/listinfo/nataphcv

      _______________________________________________



      --------------------------------------------------------------------------------


      No virus found in this incoming message.
      Checked by AVG Free Edition.
      Version: 7.5.432 / Virus Database: 268.15.26/594 - Release Date: 12/20/2006 3:54 PM


      [Non-text portions of this message have been removed]
    Your message has been successfully submitted and would be delivered to recipients shortly.