Hata Atsuko, Akashi-Ueda Ryoko, Takamatsu Kazufumi, Matsumura Takuro
Department of Pediatrics, Division of Respiratory Medicine, Kitano Hospital, The Tazuke Kofukai Medical Research Institute, Osaka, Japan ; Department of Infectious Diseases, Division of Respiratory Medicine, Kitano Hospital, The Tazuke Kofukai Medical Research Institute, Osaka, Japan.
Department of Pediatrics, Division of Respiratory Medicine, Kitano Hospital, The Tazuke Kofukai Medical Research Institute, Osaka, Japan.
Drug Des Devel Ther. 2014 Oct 24;8:2017-38. doi: 10.2147/DDDT.S46654. eCollection 2014.
This report presents a review of the efficacy and safety of peramivir, a neuraminidase inhibitor that was granted Emergency Use Authorization by the US Food and Drug Administration (FDA) from October 23, 2009 to June 23, 2010 during the 2009 H1N1 pandemic.
Literature was accessed via PubMed (January 2000-April 2014) using several search terms: peramivir; BCX-1812; RWJ 270201; H1N1, influenza; antivirals; and neuraminidase inhibitors. The peramivir manufacturers, Shionogi and Co Ltd and BioCryst Pharmaceuticals, were contacted to obtain unpublished data and information presented at recent scientific meetings. Information was obtained from the Centers for Disease Control and Prevention (CDC) and from US FDA websites. English-language and Japanese-language reports in the literature were reviewed and selected based on relevance, along with information from the CDC, US FDA, and the drug manufacturers.
We obtained eleven clinical trial reports of intravenous peramivir, two of which described comparisons with oseltamivir. Seven of nine other recently reported published studies was a dose-response study. Clinical reports of critically ill patients and pediatric patients infected with pandemic H1N1 described that early treatment significantly decreased mortality. Peramivir administered at 300 mg once daily in adult patients with influenza significantly reduces the time to alleviation of symptoms or fever compared to placebo. It is likely to be as effective as other neuraminidase inhibitors.
Although peramivir shows efficacy for the treatment of seasonal and pH1N1 influenza, it has not received US FDA approval. Peramivir is used safely and efficiently in hospitalized adult and pediatric patients with suspected or laboratory-confirmed influenza. Peramivir might be a beneficial alternative antiviral treatment for many patients, including those unable to receive inhaled or oral neuraminidase inhibitors, or those requiring nonintravenous drug delivery.
本报告对帕拉米韦的疗效和安全性进行综述。帕拉米韦是一种神经氨酸酶抑制剂,在2009年甲型H1N1流感大流行期间于2009年10月23日至2010年6月23日获得美国食品药品监督管理局(FDA)的紧急使用授权。
通过PubMed(2000年1月至2014年4月)检索文献,使用了几个检索词:帕拉米韦;BCX - 1812;RWJ 270201;H1N1、流感;抗病毒药物;以及神经氨酸酶抑制剂。联系了帕拉米韦的制造商盐野义制药株式会社和生物晶体制药公司,以获取未发表的数据和在近期科学会议上展示的信息。从疾病控制与预防中心(CDC)和美国FDA网站获取信息。对文献中的英文和日文报告进行了审查,并根据相关性进行了筛选,同时还参考了来自CDC、美国FDA和药品制造商的信息。
我们获得了11份静脉注射帕拉米韦的临床试验报告,其中两份描述了与奥司他韦的比较。其他最近报道的9项已发表研究中有7项是剂量反应研究。关于感染大流行H1N1的重症患者和儿科患者的临床报告表明,早期治疗显著降低了死亡率。与安慰剂相比,在成年流感患者中每日一次给予300mg帕拉米韦可显著缩短症状缓解或退热时间。它可能与其他神经氨酸酶抑制剂一样有效。
尽管帕拉米韦对季节性流感和pH1N1流感的治疗显示出疗效,但尚未获得美国FDA的批准。帕拉米韦在疑似或实验室确诊流感的住院成年和儿科患者中使用安全有效。对于许多患者,包括那些无法接受吸入或口服神经氨酸酶抑制剂的患者,或那些需要非静脉给药的患者,帕拉米韦可能是一种有益的抗病毒替代治疗方法。