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AWZ1066S a highly specific anti-Wolbachia drug candidate for a short-course treatment of filariasis

机译:AWZ1066S一种用于短程丝虫病的高特异性抗沃尔巴氏菌候选药物

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摘要

Onchocerciasis and lymphatic filariasis are two neglected tropical diseases that together affect ∼157 million people and inflict severe disability. Both diseases are caused by parasitic filarial nematodes with elimination efforts constrained by the lack of a safe drug that can kill the adult filaria (macrofilaricide). Previous proof-of-concept human trials have demonstrated that depleting >90% of the essential nematode endosymbiont bacterium, Wolbachia, using antibiotics, can lead to permanent sterilization of adult female parasites and a safe macrofilaricidal outcome. AWZ1066S is a highly specific anti-Wolbachia candidate selected through a lead optimization program focused on balancing efficacy, safety and drug metabolism/pharmacokinetic (DMPK) features of a thienopyrimidine/quinazoline scaffold derived from phenotypic screening. AWZ1066S shows superior efficacy to existing anti-Wolbachia therapies in validated preclinical models of infection and has DMPK characteristics that are compatible with a short therapeutic regimen of 7 days or less. This candidate molecule is well-positioned for onward development and has the potential to make a significant impact on communities affected by filariasis.
机译:盘尾丝虫病和淋巴丝虫病是两种被忽视的热带病,共影响约1.57亿人,并造成严重的残疾。两种疾病均由寄生的丝虫线虫引起,其消除工作受到缺乏可以杀死成年丝虫的安全药物(宏杀螨剂)的限制。之前的概念验证性人体试验表明,使用抗生素消耗超过90%的线虫内共生细菌即Wolbachia可以导致成年雌性寄生虫永久性绝育和安全的杀大型杀线虫剂。 AWZ1066S是通过领先的优化程序选择的高度特异性的抗Wolbachia候选药物,该程序专注于平衡源自表型筛选的噻吩并嘧啶/喹唑啉支架的功效,安全性和药物代谢/药代动力学(DMPK)特征。 AWZ1066S在经过验证的感染临床前模型中显示出优于现有抗沃尔巴氏菌疗法的功效,并且具有与7天或更短的短期治疗方案兼容的DMPK特性。该候选分子定位良好,可继续发展,并有可能对受丝虫病影响的社区产生重大影响。

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