Learning Objectives
Upon completion of this activity, participants should be able to:
- Cite new findings on the safety and efficacy of investigational antiviral agents including protease inhibitors and nonnucleoside polymerase inhibitors in patients with chronic HCV infection
- Recount the latest results on the optimal treatment duration for HCV-infected patients who experience a slow response to peginterferon/ribavirin therapy
- Discuss the relationship between on-treatment hemoglobin decreases, erythropoietin use, and virologic response among patients with chronic HCV infection
- Summarize the results of recent clinical trials evaluating new approaches to treating and managing complications associated with advanced liver disease such as hepatic encephalopathy
- Articulate the latest findings on the optimal timing of treatment for patients with acute hepatitis C infection
Topics covered include:
- SPRINT-1: Boceprevir and Peginterferon alfa-2b/Ribavirin in Treatment-Naive Patients With Genotype 1 HCV
- PROVE 3: Telaprevir Plus Peginterferon alfa-2a/Ribavirin in Previously Treated Patients With Genotype 1 HCV
- ITMN-191 Plus Peginterferon alfa-2a/Ribavirin in Treatment-Naive Patients Infected With Genotype 1 HCV
- SCH 900518 With or Without Ritonavir Plus Peginterferon alfa-2b in Treatment-Naive and Treatment-Experienced Patients With Genotype 1 HCV Infection
- Efficacy and Safety of Investigational Nonnucleoside Polymerase Inhibitors
- Albinterferon alfa-2b vs Peginterferon alfa-2a in Treatment-Naive Patients With Genotype 1 HCV
- 48 vs 72 Weeks of Peginterferon alfa-2b/Ribavirin in Slow Responders Infected with Genotype 1 HCV
- On-Treatment Hemoglobin Decline, Erythropoietin Use, and Virologic Response to Peginterferon/Ribavirin Therapy
- Rifaximin for the Prevention of Recurrent Hepatic Encephalopathy
- Immediate vs Delayed Treatment of Acute HCV Infection
- High-Dose Ursodeoxycholic Acid Treatment for Nonalcoholic Steatohepatitis
Abstract