Scroll Up
Scroll Down
Play Play Play Play
Unregistered User
Click here if this is not your Personal Edition
 
Contact Us | Free E-Mail Updates | Journals | Register a colleague
 
 
Hepatitis C
 
   
 
SEARCH   
Doctor's Guide Free CME
Medline
Congress Resource Centre
 

 EXPLORE :
   Most Read News
 All News  All News
 All Webcasts / CME  All Webcasts / CME
 All Cases  All Cases
 Congress Resource Centre  Congress Resource Centre
 All Medical Resources  All Medical Resources
 Medical  My Personal Edition



Warning | Privacy

 

 
 Recent news - Hepatitis C
    TopAbstracts in Hepatitis C 11/10/2009 - (DGNews)
    Choice of Calcineurin Inhibitor Does Not Influence Outcome of Liver Transplantation in HCV-Positive Recipients: Presented at AASLD - (DGDispatch)
    What Is the Optimal Timing of Hepatitis C Antiviral Therapy Before and After Liver Transplantation? Presented at AASLD - (DGDispatch)
    Viral Load Predicts Outcome of Liver Transplant Recipients With Hepatitis C: Presented at AASLD - (DGDispatch)
    Post-transplant Prophylactic Antiviral Treatment Does Not Prevent Recurrent Hepatitis C: Presented at AASLD - (DGDispatch)

    News archive

     Recent webcasts/CME - Hepatitis C
    • Improving the Standard of Care for HCV Management: Available and Emerging Strategies for Optimal Patient Outcomes
    • Improving Outcomes in Hepatitis C
    • Issues in the Care of HIV and Hepatitis C Virus-coinfected Patients: Antiretroviral Pharmacokinetics, Drug Interactions, and Liver Transplantation
      Cancer, Liver, Infections, Cardiovascular Disease, and other Biologic Agents
      Treating a Patient with RA and Hepatitis B or C

      Webcasts/CME archive

       Recent cases - Hepatitis C
        Pseudoleukocytosis Secondary to Hepatitis C-Associated Cryoglobulinemia: A Case Report
        Primary Central Nervous System Lymphoma Presenting as Bilateral Uveitis in an Immunocompetent HCV+ Patient: A Case Report
        Intra-Hepatic Splenosis as an Unexpected Cause of a Focal Liver Lesion in a Patient with Hepatitis C and Liver Cirrhosis: A Case Report
        Hepatitis Following Famotidine: A Case Report
        Hepatic Splenosis Mimicking HCC in a Patient with Hepatitis C Liver Cirrhosis and Mildly Raised Alpha Feto Protein; the Important Role of Explorative Laparoscopy

        Cases archive
          




        my personal edition > hepatitis c > news
        divider

          E-Mail this DGNews to a colleague

        DGNews


        FDA Approves PEG-IFN Alfa-2b/Ribavirin Combination Therapy for Paediatric HCV

          NEW YORK -- December 12, 2008 -- The US Food and Drug Administration (FDA) has approved pegylated interferon alfa-2b (PEG-IFN [Pegintron]) and ribavirin (Rebetol) combination therapy for use in previously untreated patients aged 3 years of age and older with chronic hepatitis C virus (HCV).

          The approval for the paediatric indication is based on the results of a clinical trial in 107 previously untreated patients aged 3 to 17 years with chronic hepatitis C and compensated liver disease.

          In the study, patients infected with HCV genotype 1 or 4 and those with HCV genotype 3 with HCV RNA greater than 600,000 IU/mL were assigned 48 weeks of therapy, while those infected with HCV genotype 2 or 3 with HCV RNA less than 600,000 IU/mL received 24 weeks of therapy.

          Of the patients with HCV genotype 1, 4 or 3 high viral load (HVL) who were assigned to 48 weeks of treatment, 55% achieved sustained viral response (SVR). As with adult patients, SVR in paediatric patients with HCV genotype 2 or 3 low viral load (LVL) was much higher than in those with genotype 1; the SVR rate was 96% in children with HCV genotype 2 or 3 LVL.

          Patients receiving PEG-IFN alfa-2b combination therapy (excluding those with HCV genotype 2 or 3) should be discontinued from therapy at week 12 if their HCV RNA dropped less than 2 log10 compared to pretreatment or at 24 weeks if they have detectable HCV RNA at treatment week 24.

          During the course of therapy lasting up to 48 weeks, weight loss and growth inhibition were common. Some children who experienced growth inhibition during therapy still had inhibited growth velocity 6 months following the end of treatment.

          Most common adverse reactions (>25%) observed in these studies were pyrexia, headache, neutropenia, fatigue, anorexia, injection-site erythema, and vomiting. Three percent were treated for clinical hypothyroidism.

          Dose modifications were required in 25% of patients, most commonly for anaemia, neutropenia, and weight loss. Therapy was discontinued prematurely in 2% of the patients.

          SOURCE Schering-Plough Corporation




        E-Mail this DGNews to a colleague   To print, use this version






        All contents Copyright (c) 1995-2009 Doctor's Guide Publishing Limited. All rights reserved.



        The NTK initiative. Physicians helping physicians identify Need-To-Know science
           Feedback
        Please rate this article: Strongly DISAGREE...Strongly AGREE NTK logo
        Question 1 - Physicians need to become aware of this information as soon as possible. Question 2 - This information is likely to have an impact on the way physicians practice medicine.
        1
        2
        3
        4
        5
        6
        7
        Send