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Efficacy of Initial Treatment with Clevudine in Naive Patients with Chronic Hepatitis B

  • Yang, Hyeon-Woong (Department of Internal Medicine, Eulji University School of Medicine) ;
  • Lee, Byung-Seok (Department of Internal Medicine, Chungnam National University School of Medicine) ;
  • Lee, Tae-Hee (Department of Internal Medicine, Konyang University College of Medicine) ;
  • Lee, Heon-Young (Department of Internal Medicine, Chungnam National University School of Medicine) ;
  • Nam, Kwan-Woo (Department of Internal Medicine, Chungnam National University School of Medicine) ;
  • Kang, Young-Woo (Department of Internal Medicine, Konyang University College of Medicine) ;
  • Chae, Hee-Bok (Department of Internal Medicine, Chungbuk National University College of Medicine) ;
  • Kim, Seok-Hyun (Department of Internal Medicine, Chungnam National University School of Medicine) ;
  • Kim, Seok-Bae (Department of Internal Medicine, Dankook University College of Medicine) ;
  • Lee, Hyang-Ie (Department of Internal Medicine, Eulji University School of Medicine) ;
  • Kim, An-Na (Department of Internal Medicine, Eulji University School of Medicine) ;
  • Song, Il-Han (Department of Internal Medicine, Dankook University College of Medicine) ;
  • Lee, Sae-Hwan (Department of Internal Medicine, Soonchunhyang University College of Medicine) ;
  • Kim, Hong-Su (Department of Internal Medicine, Soonchunhyang University College of Medicine)
  • Received : 2009.12.31
  • Accepted : 2010.09.14
  • Published : 2010.12.01

Abstract

Background/Aims: Clevudine, a pyrimidine nucleoside analogue, has potent antiviral effects in patients with chronic viral hepatitis B (CHB). We report the efficacy of initial treatment with clevudine in naive patients with CHB living in Daejeon and Chungcheong Province, South Korea. Methods: One hundred five adults with CHB were administered 30 mg of clevudine per day for an average of 51 weeks. We evaluated viral markers and liver biochemistry retrospectively every 3 months. Results: Alanine aminotransferase (ALT), aspartate aminotransferase (AST), and hepatitis B virus (HBV) DNA before the treatment were $184{\pm}188$ IU/L, $150{\pm}138$ IU/L, and $7.1{\pm}1.2$ log copies/mL, respectively. Undetectable rates (< 60 IU/mL) of DNA were 36.2%, 68.9%, 83.6%, 76.2%, and 75.8% at 12, 24, 36, 48, and 60 weeks, respectively. Seroconversion rates were 9.1%, 13.6%, 24.6%, 26.5%, and 26.1% and ALT normalization rates were 64.5%, 78.1%, 87.9%, 90.0% at 12, 24, 36, and 48 weeks, respectively. Six patients (5.7%) had a viral breakthrough. Conclusions: Clevudine is a useful drug in the initial treatment of patients with CHB, with a potent antiviral effect and low incidence of viral breakthrough.

Keywords

References

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  1. Drugs in Development for the Treatment of Chronic Hepatitis B vol.11, pp.2, 2010, https://doi.org/10.1007/s11901-012-0131-9
  2. Long-Term Treatment Efficacy and Safety of Clevudine Therapy in Naïve Patients with Chronic Hepatitis B vol.6, pp.4, 2010, https://doi.org/10.5009/gnl.2012.6.4.486
  3. Efficacy of Entecavir Switching Therapy in Chronic Hepatitis B Patients with Clevudine-induced Myopathy vol.61, pp.1, 2010, https://doi.org/10.4166/kjg.2013.61.1.30