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A 12-week clevudine therapy showed potent and durable antiviral activity in HBeAg-positive chronic hepatitis B

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dc.contributor.authorLee, Hyo-Suk-
dc.contributor.authorChung, Young-Hwa-
dc.contributor.authorLee, Kwansik-
dc.contributor.authorByun, Kwan Soo-
dc.contributor.authorPaik, Seung Woon-
dc.contributor.authorHan, Joon-Yeol-
dc.contributor.authorYoo, Kwon-
dc.contributor.authorYoo, Hee-Won-
dc.contributor.authorLee, Jin Heon-
dc.contributor.authorYoo, Byung Chul-
dc.date.accessioned2010-01-08T07:59:05Z-
dc.date.available2010-01-08T07:59:05Z-
dc.date.issued2006-04-22-
dc.identifier.citationHepatology. 2006 May;43(5):982-8.en
dc.identifier.issn0270-9139 (Print)-
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=16628625-
dc.identifier.urihttps://hdl.handle.net/10371/29007-
dc.description.abstractClevudine is a nucleoside analog with an unnatural beta-L configuration. In a phase I/II clinical trial, once daily doses ranging from 10 to 200 mg for 28 days were well tolerated, and produced significant antiviral activity. The present study was conducted to assess the degree and durability of the antiviral response to 12 weeks of clevudine treatment, and to investigate its safety and tolerability. A total of 98 patients with HBeAg-positive chronic hepatitis B were randomized to placebo (n=32), 30-mg clevudine (n=32), and 50-mg clevudine (n=34) groups. Patients were followed up after 12 weeks of treatment for a further 24 weeks off-therapy. Median serum hepatitis B virus DNA reductions from baseline at week 12 were 0.20, 4.49, and 4.45 log10 copies/mL in the placebo, 30-mg clevudine, and 50-mg clevudine groups, respectively (P < .0001). Posttreatment antiviral activities were sustained, with 3.32 and 2.99 log10 reductions at week 12 off-therapy and 2.28 and 1.40 log10 reductions at week 24 off-therapies in the 30- and 50-mg clevudine groups, respectively. Median serum alanine aminotransferase (ALT) levels decreased markedly from baseline during clevudine treatment and were maintained below the upper limit of normal throughout the 24 weeks off-therapy in the two clevudine-treated groups. The incidences of adverse events and treatment-emergent grade 3 or 4 laboratory abnormalities were similar for the three groups. In conclusion, clevudine showed potent antiviral activity during therapy and induced a sustained posttreatment antiviral effect for 6 months after a 12-week treatment period, and this was associated with a sustained normalization of ALT levels.en
dc.language.isoenen
dc.publisherWiley-Blackwellen
dc.subjectAdulten
dc.subjectAntiviral Agents/*therapeutic useen
dc.subjectArabinofuranosyluracil/*analogs & derivatives/therapeutic useen
dc.subjectFemaleen
dc.subjectHepatitis B e Antigens/*blooden
dc.subjectHepatitis B, Chronic/*blood/*drug therapyen
dc.subjectMaleen
dc.subjectTime Factorsen
dc.subjectHumansen
dc.titleA 12-week clevudine therapy showed potent and durable antiviral activity in HBeAg-positive chronic hepatitis Ben
dc.typeArticleen
dc.contributor.AlternativeAuthor이효석-
dc.contributor.AlternativeAuthor정영화-
dc.contributor.AlternativeAuthor이관식-
dc.contributor.AlternativeAuthor변관수-
dc.contributor.AlternativeAuthor백승운-
dc.contributor.AlternativeAuthor한준열-
dc.contributor.AlternativeAuthor유권-
dc.contributor.AlternativeAuthor유희원-
dc.contributor.AlternativeAuthor이진헌-
dc.contributor.AlternativeAuthor유병철-
dc.identifier.doi10.1002/hep.21166-
Appears in Collections:
College of Medicine/School of Medicine (의과대학/대학원)Internal Medicine (내과학전공)Journal Papers (저널논문_내과학전공)
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