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巴洛沙韦酯:一种用于治疗急性非复杂性流感的新型帽依赖性核酸内切酶(CEN)抑制剂。

Baloxavir marboxil: a novel cap-dependent endonuclease (CEN) inhibitor for the treatment of acute uncomplicated influenza.

作者信息

Locke S C, Splawn L M, Cho J C

机构信息

The University of Texas at Tyler, College of Pharmacy, Tyler, Texas, USA.

出版信息

Drugs Today (Barc). 2019 Jun;55(6):359-366. doi: 10.1358/dot.2019.55.6.2999889.

Abstract

Baloxavir marboxil is a newly approved antiviral agent with activity against influenza via a novel mechanism of action of inhibition of cap-dependent endonuclease (CEN). The novel agent was approved in October of 2018 in the United States for the treatment of acute uncomplicated influenza A and B in patients aged 12 years or older. Baloxavir is given as a single weight-based dose of 40 mg orally once for patients weighing less than 80 kg and 80 mg orally once for those weighing 80 kg or more within 48 hours of symptom onset. In comparison with current therapy, baloxavir is as effective in decreasing time to symptom alleviation as the drug of choice, oseltamivir, and significantly reduces viral load 1 day after treatment compared with placebo and oseltamivir. In safety analyses baloxavir was well tolerated with only mild adverse events reported (nausea, headache, diarrhea, bronchitis, nasopharyngitis), thus providing a safe and reliable alternative option to current therapy for acute uncomplicated influenza. Further studies are being conducted to evaluate the use of baloxavir in additional patient populations including pediatric patients less than 12 years of age and patients who are at high risk of complications related to influenza.

摘要

巴洛沙韦酯是一种新获批的抗病毒药物,通过抑制帽依赖性核酸内切酶(CEN)这一新型作用机制发挥抗流感活性。该新型药物于2018年10月在美国获批,用于治疗12岁及以上患者的急性单纯性甲型和乙型流感。对于症状出现48小时内体重小于80kg的患者,巴洛沙韦按基于体重的单次剂量40mg口服给药一次;对于体重80kg及以上的患者,则单次口服80mg。与目前的治疗方法相比,巴洛沙韦在缩短症状缓解时间方面与首选药物奥司他韦效果相当,且与安慰剂和奥司他韦相比,治疗1天后可显著降低病毒载量。在安全性分析中,巴洛沙韦耐受性良好,仅报告了轻微不良事件(恶心、头痛、腹泻、支气管炎、鼻咽炎),因此为急性单纯性流感的当前治疗提供了一种安全可靠的替代选择。正在进行进一步研究,以评估巴洛沙韦在其他患者群体中的应用,包括12岁以下的儿科患者以及有流感相关并发症高风险的患者。

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