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巴洛沙韦马立克韦:急性单纯性流感的综述。

Baloxavir Marboxil: A Review in Acute Uncomplicated Influenza.

机构信息

Springer Nature, Private Bag 65901, Mairangi Bay, Auckland, 0754, New Zealand.

出版信息

Drugs. 2020 Jul;80(11):1109-1118. doi: 10.1007/s40265-020-01350-8.

Abstract

Baloxavir marboxil (Xofluza; hereafter referred to as baloxavir), the prodrug of baloxavir acid, is a first-in-class, small molecule inhibitor of the polymerase acidic (PA) protein subunit of the influenza virus polymerase complex. Baloxavir (after conversion to baloxavir acid) acts to block influenza virus replication by inhibiting the cap-dependent endonuclease activity of the PA protein. Taken orally as a single dose, baloxavir is approved in the USA for the treatment of acute uncomplicated influenza in patients ≥ 12 years of age who have been symptomatic for ≤ 48 h. Data from randomized, double-blind, placebo- and oseltamivir-controlled phase III trials have shown that baloxavir is efficacious in improving influenza symptoms both in otherwise healthy adolescents and adults and in those at high risk of influenza complications, displaying similar efficacy to that of oseltamivir. Furthermore, there is evidence that baloxavir can reduce influenza viral load more rapidly than oseltamivir. Baloxavir has activity against influenza A and B viruses (including strains resistant to neuraminidase inhibitors) and is well tolerated. Evidence of the emergence and likely human-to-human transmission of variant viruses with reduced susceptibility to baloxavir highlights the importance of monitoring and surveillance for changes in influenza virus drug susceptibility patterns. However, currently available evidence suggests that baloxavir, with the benefits of a single oral dose regimen, provides a useful alternative to neuraminidase inhibitors for the treatment of acute uncomplicated influenza in adolescents and adults.

摘要

巴洛沙韦马索利(Xofluza;以下简称巴洛沙韦)是流感病毒聚合酶酸性(PA)蛋白亚单位的前药,属于首个上市的小分子聚合酶抑制剂。巴洛沙韦(转化为巴洛沙韦酸后)通过抑制 PA 蛋白的帽依赖性内切酶活性来阻止流感病毒的复制。作为单一剂量口服,巴洛沙韦在美国被批准用于治疗症状出现≤48 小时的 12 岁及以上急性单纯性流感患者。来自随机、双盲、安慰剂和奥司他韦对照的 III 期临床试验的数据表明,巴洛沙韦在改善健康青少年和成年人以及流感并发症高危人群的流感症状方面是有效的,其疗效与奥司他韦相似。此外,有证据表明,巴洛沙韦可以比奥司他韦更快地降低流感病毒载量。巴洛沙韦对甲型和乙型流感病毒(包括对神经氨酸酶抑制剂耐药的菌株)均有效,且具有良好的耐受性。对具有降低的巴洛沙韦敏感性的变异病毒的出现和可能的人际传播的证据突显了监测流感病毒药物敏感性模式变化的重要性。然而,目前的证据表明,巴洛沙韦具有单剂量口服给药方案的优势,可为青少年和成年急性单纯性流感的治疗提供除神经氨酸酶抑制剂之外的有用选择。

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