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RWJ-270201 (BCX-1812): a novel neuraminidase inhibitor for influenza.

机译:RWJ-270201(BCX-1812):一种新型的流感神经氨酸酶抑制剂。

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摘要

The influenza virus neuraminidase (NA) is important in the pathogenesis of infection and, thus, is an attractive target for agents used in the treatment and prophylaxis of influenza. This article describes preclinical and early clinical data related to RWJ-270201 (BCX-1812), a novel, orally active NA inhibitor that was rationally designed for having potent and selective activity against influenza A and B viruses. RWJ-270201 is a unique NA inhibitor with a cyclopentane ring structure and high selectivity for the influenza NA. RWJ-270201 has efficacy comparable to or better than earlier NA inhibitors against a wide range of influenza A and B isolates, including recently emerged and avian strains, both in vitro and in a lethal murine model of influenza. Based on the high selectivity and efficacy of RWJ-270201 against both type A and B influenza strains in preclinical studies as well as murine pharmacodynamic studies supporting the potential for once-daily administration, clinical trials were initiated in order to determine the tolerability and antiviral activity of RWJ-270201 in humans. To date, clinical studies have indicated that RWJ-270201 is well tolerated and has antiviral activity in human experimental influenza models when administered orally once daily.
机译:流感病毒神经氨酸酶(NA)在感染的发病机理中很重要,因此,是用于治疗和预防流感的药物的有吸引力的靶标。本文介绍了与RWJ-270201(BCX-1812)有关的临床前和早期临床数据,RWJ-270201(BCX-1812)是一种新颖的口服活性NA抑制剂,经过合理设计,具有对A和B型流感病毒的有效和选择性活性。 RWJ-270201是一种独特的NA抑制剂,具有环戊烷环结构和对流感NA的高选择性。 RWJ-270201在体外和致死性鼠源性流感模型中,对广泛的甲型和乙型流感病毒分离株(包括最近出现的和禽流感病毒株)具有与早期NA抑制剂相当或更高的功效。基于RWJ-270201在临床前研究以及支持每天一次给药潜力的鼠药效学研究中对A型和B型流感病毒株的高选择性和有效性,启动了临床试验以确定耐受性和抗病毒活性RWJ-270201在人类中的表达。迄今为止,临床研究表明,当每天口服一次时,RWJ-270201具有良好的耐受性,并且在人实验流感模型中具有抗病毒活性。

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