https://scholars.lib.ntu.edu.tw/handle/123456789/568419
標題: | Randomized, controlled pharmacokinetic and pharmacodynamic evaluation of albinterferon in patients with chronic hepatitis B infection | 作者: | Colvin R.A. Tanwandee T. Piratvisuth T. Thongsawat S. Hui A.J. Zhang H. Ren H. PEI-JER CHEN Chuang W.-L. Sobhonslidsuk A. Li R. Qi Y. Praestgaard J. Han Y. Xu J. Stein D.S. Chien R.-N. Flisiak R. Jablkowski M. Liaw Y.-F. Sung J.J.-Y. |
關鍵字: | Albinterferon; Hepatitis B; Lung diffusion capacity | 公開日期: | 2015 | 出版社: | Blackwell Publishing | 卷: | 30 | 期: | 1 | 起(迄)頁: | 184-191 | 來源出版物: | Journal of Gastroenterology and Hepatology (Australia) | 摘要: | Background and Aims: Albinterferon is a fusion of albumin and interferon-α2b developed to improve the pharmacokinetics, convenience, and potential efficacy of interferon-α for the treatment of chronic hepatitis infections. Methods: This open-label, randomized, active-controlled, multicenter study investigated the safety and efficacy of albinterferon in patients with chronic hepatitis B virus (HBV) infection who were e-antigen (HBeAg) positive. One hundred and forty-one patients received one of four albinterferon doses/regimens or pegylated-interferon-α2a. Primary efficacy outcomes were changes in serum HBeAg and antibody, HBV-DNA, and alanine aminotransferase. Principal safety outcomes were changes in laboratory values, pulmonary function, and adverse events. Results: The study was prematurely terminated as phase III trials in hepatitis C infection indicated noninferior efficacy but inferior safety compared with pegylated-interferon-α2a. Here, all treatment groups had a significant reduction in HBV-DNA from baseline. Reductions in HBV-DNA were not significantly different, except the 1200μg every 4 weeks albinterferon dose which was inferior compared with pegylated-interferon-α2a. The serum alanine aminotransferase levels decreased in all arms. The per-patient incidence of adverse events was not significantly different for albinterferon (96.4-100%) and pegylated-interferon-α2a (93.1%). Total adverse events, however, were higher for albinterferon and correlated to dose. Decreased lung function was found in all arms (?93% of patients), and was more common in some albinterferon groups. Conclusions: Albinterferon doses with similar anti-HBV efficacy to pegylated-interferon-α2a had higher rates of certain adverse events, particularly changes in lung diffusion capacity (http://www.clinicaltrials.gov number NCT00964665). ? 2014 Journal of Gastroenterology and Hepatology Foundation and Wiley Publishing Asia Pty Ltd. |
URI: | https://www.scopus.com/inward/record.uri?eid=2-s2.0-84919608802&doi=10.1111%2fjgh.12671&partnerID=40&md5=a095e4bb32bc5c9803ddffb4fd02eff6 https://scholars.lib.ntu.edu.tw/handle/123456789/568419 |
ISSN: | 0815-9319 | DOI: | 10.1111/jgh.12671 | SDG/關鍵字: | peginterferon alpha2a; alanine aminotransferase; albinterferon alpha2b; albuminoid; alpha interferon; antivirus agent; biological marker; hepatitis B(e) antigen; macrogol derivative; peginterferon alpha2a; recombinant protein; virus DNA; adult; aged; alanine aminotransferase blood level; Article; drug safety; drug tolerability; female; flu like syndrome; follow up; good clinical practice; hepatitis B; human; limit of detection; lung diffusion capacity; lung function; major clinical study; male; polymerase chain reaction; post hoc analysis; priority journal; risk assessment; blood; clinical trial; comparative study; controlled study; genetics; Hepatitis B virus; Hepatitis B, Chronic; immunology; multicenter study; randomized controlled trial; treatment outcome; virology; young adult; Adult; Alanine Transaminase; Albumins; Antiviral Agents; Biological Markers; DNA, Viral; Female; Hepatitis B e Antigens; Hepatitis B virus; Hepatitis B, Chronic; Humans; Interferon-alpha; Male; Polyethylene Glycols; Recombinant Proteins; Treatment Outcome; Young Adult |
顯示於: | 臨床醫學研究所 |
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