نتایج جستجو برای: asunaprevir

تعداد نتایج: 282  

Journal: :Antimicrobial agents and chemotherapy 2012
Fiona McPhee Amy K Sheaffer Jacques Friborg Dennis Hernandez Paul Falk Guangzhi Zhai Steven Levine Susan Chaniewski Fei Yu Diana Barry Chaoqun Chen Min S Lee Kathy Mosure Li-Qiang Sun Michael Sinz Nicholas A Meanwell Richard J Colonno Jay Knipe Paul Scola

Asunaprevir (ASV; BMS-650032) is a hepatitis C virus (HCV) NS3 protease inhibitor that has demonstrated efficacy in patients chronically infected with HCV genotype 1 when combined with alfa interferon and/or the NS5A replication complex inhibitor daclatasvir. ASV competitively binds to the NS3/4A protease complex, with K(i) values of 0.4 and 0.24 nM against recombinant enzymes representing geno...

Journal: :Hepatology research : the official journal of the Japan Society of Hepatology 2017
Masaki Honda Yasuhiko Sugawara Takehisa Watanabe Masakuni Tateyama Motohiko Tanaka Koushi Uchida Seiichi Kawabata Daiki Yoshii Kouhei Miura Kaori Isono Shintaro Hayashida Yuki Ohya Hidekazu Yamamoto Yutaka Sasaki Yukihiro Inomata

AIM The development of direct-acting oral agents has dramatically changed the treatment strategy of hepatitis C virus (HCV) infection. Here we aimed to reveal the efficacy and safety of daclatasvir (DCV) and asunaprevir (ASV) for recurrent HCV genotype 1 infection after liver transplantation (LT). METHODS A retrospective study was undertaken on nine patients who underwent a 24-week DCV/ASV tr...

2016
Hee Chul Nam Hae Lim Lee Hyun Yang Myeong Jun Song

BACKGROUND/AIMS The treatment strategy for hepatitis C virus (HCV) has been changing rapidly since the introduction of direct-acting antivirals such as daclatasvir (DCV) and asunaprevir (ASV). We evaluated the efficacy and safety of DCV and ASV for HCV in real-life practice. METHODS Patients were treated with 60 mg of DCV once daily plus 200 mg of ASV twice daily for 24 weeks, and followed fo...

2013
Hee Bok Chae Seon Mee Park Sei Jin Youn

Currently, two direct-acting antivirals (DAAs) show well-established efficacy against hepatitis C virus (HCV), namely, first-wave protease inhibitors telaprevir and boceprevir. Most clinical trials have examined DAAs in combination with standard of care (SOC) regimens. Future therapeutic drugs were divided into three categories. They are second-wave protease inhibitors, second-generation protea...

2017
Yugo Kai Hayato Hikita Naoki Morishita Kazuhiro Murai Tasuku Nakabori Sadaharu Iio Hideki Hagiwara Yasuharu Imai Shinji Tamura Syusaku Tsutsui Masafumi Naito Meiko Nishiuchi Yasuteru Kondo Takanobu Kato Hiroshi Suemizu Ryoko Yamada Tsugiko Oze Takayuki Yakushijin Naoki Hiramatsu Ryotaro Sakamori Tomohide Tatsumi Tetsuo Takehara

Resistance-associated substitutions (RASs) in hepatitis C virus (HCV) appear upon failure of treatment with direct-acting antivirals (DAAs). However, their origin has not been clarified in detail. Among 11 HCV genotype 1b patients who experienced virologic failure with asunaprevir (ASV)/daclatasvir (DCV), 10 had major NS5A L31M/V-Y93H variants after treatment. L31M/V-Y93H variants were detected...

2016
Xingquan Zhang

Unlike human immunodeficiency virus (HIV) and hepatitis B virus (HBV), hepatitis C virus (HCV) infection is a curable disease. Current direct antiviral agent (DAA) targets are focused on HCV NS3/4A protein (protease), NS5B protein (polymerase) and NS5A protein. The first generation of DAAs includes boceprevir and telaprevir, which are protease inhibitors and were approved for clinical use in 20...

2017
Haruhiko Takeda Yoshihide Ueda Tadashi Inuzuka Yukitaka Yamashita Yukio Osaki Akihiro Nasu Makoto Umeda Ryo Takemura Hiroshi Seno Akihiro Sekine Hiroyuki Marusawa

Resistance-associated variant (RAV) is one of the most significant clinical challenges in treating HCV-infected patients with direct-acting antivirals (DAAs). We investigated the viral dynamics in patients receiving DAAs using third-generation sequencing technology. Among 283 patients with genotype-1b HCV receiving daclatasvir + asunaprevir (DCV/ASV), 32 (11.3%) failed to achieve sustained viro...

2014
Yoshihito Uchida Jun-ichi Kouyama Kayoko Naiki Satoshi Mochida

AIM Oral treatment with asunaprevir and daclatasvir has been reported to yield a SVR ratio of 80% in patients with genotype 1b HCV infection, however, treatment failure has been reported, especially in patients with HCV strains showing the NS5A-Y93H mutation at baseline. An assay system to detect such strains was established to facilitate selection of appropriate candidates for this antiviral t...

2015
Kazuaki Chayama C. Nelson Hayes Thomas F. Baumert

Sustained virological response (SVR) rates have increased dramatically following the approval of direct acting antiviral (DAA) therapies. While individual DAAs have a low barrier to resistance, most patients can be successfully treated using DAA combination therapy. However, DAAs are vulnerable to drug resistance, and resistance-associated variants (RAVs) may occur naturally prior to DAA therap...

2018
Takeshi Chida Kazuhito Kawata Kazuyoshi Ohta Erika Matsunaga Jun Ito Shin Shimoyama Satoru Yamazaki Hidenao Noritake Tetsuro Suzuki Takafumi Suda Yoshimasa Kobayashi

Background/Aims Changes in lipid profiles in patients infected with hepatitis C virus (HCV) during direct-acting antiviral therapy have been reported in recent years. However, the clinical aspects of disturbed lipid metabolism in chronic HCV infection have not been fully elucidated. Methods Dynamic changes in serum total, low-density lipoprotein (LDL), and high-density lipoprotein (HDL) chole...

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