默沙东MK-5172/MK-8742治疗HIV/HCV感染疗效强劲

2014-03-07 tomato 生物谷

默沙东(Merck & Co)3月6日公布了一项正在开展的II期研究(C-WORTHY Study)的新数据。该研究调查了丙型肝炎全口服组合疗法(MK-5172/MK-8742)用于治疗HIV/HCV合并感染的疗效和安全性。研究中,HIV/HCV合并感染患者接受了12周MK-5172/MK-8742治疗后,取得了强劲的HCV抑制,表明该组合疗法用于治疗HIV/HCV合并感染非常有效,同时,

默沙东(Merck & Co)3月6日公布了一项正在开展的II期研究(C-WORTHY Study)的新数据。该研究调查了丙型肝炎全口服组合疗法(MK-5172/MK-8742)用于治疗HIV/HCV合并感染的疗效和安全性。研究中,HIV/HCV合并感染患者接受了12周MK-5172/MK-8742治疗后,取得了强劲的HCV抑制,表明该组合疗法用于治疗HIV/HCV合并感染非常有效,同时,安全性与单纯HCV基因型1感染组中所观察到的一致。

在治疗的12周,HIV/HCV合并感染群体,MK-5172/MK-8742+利巴韦林(RBV)联合治疗组100%(29/29)HCV RNA水平低于25 IU/毫升,MK-5172/MK-8742治疗组为90%(26/29);HCV单独感染群体,MK-5172/MK-8742治疗组100%(13/13)HCV RNA水平低于25 IU/毫升。相关数据已提交至第21届逆转录病毒和机会性感染大会(CROI 2014)。

MK-5172和MK-8742均属于非常有前途的新一类抗病毒药物。MK-5172是一种实验性HCV NS3/4A蛋白酶抑制剂,MK-8742则是一种实验性HCV NS5A复制复合体抑制剂。此前,FDA于2013年10月授予MK-5172/MK-8742全口服方案突破性疗法认定。

慢性丙型肝炎是默沙东研发的优先重点。目前,该公司正在一个广泛的临床项目中评价MK-5172和MK-8742,包括多种HCV基因型感染初治患者、治疗失败的患者、以及其他重要的HCV亚群,如肝硬化和HCV/HIV合并感染。

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    2014-03-09 ymljack
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    2014-03-09 yese
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