School of Animal and Comparative Biomedical Sciences Valley Fever Center for Excellence.
Valley Fever Center for Excellence.
J Infect Dis. 2014 Jun 15;209(12):1949-54. doi: 10.1093/infdis/jiu029. Epub 2014 Jan 12.
Nikkomycin Z (NikZ) is a chitin synthase inhibitor with activity against Coccidioides species that is being developed as a first-in-class orphan product for treatment of coccidioidomycosis. It has previously been shown to reduce lethal respiratory infections in mice to undetectable levels when treatment is begun 48 hours after infection. The studies described here focus on bracketing NikZ doses for phase 2 and 3 clinical trials, using an established mouse respiratory infection as a model and starting treatment 120 hours after infection. A dose of 80 mg/kg/day, divided into 2 doses, nearly eradicated infection, and larger doses did not improve fungal clearance. Increasing the duration of treatment from 1 week to 3 weeks resulted in a greater percentage of culture-negative mice. Comparative data show that plasma levels of NikZ that nearly eradicate Coccidioides in mice are achievable in patients and provide a plausibly effective dose range for initial phase 2 clinical studies.
尼可霉素 Z(NikZ)是一种几丁质合成酶抑制剂,对新型隐球菌属具有活性,目前正在开发为治疗球孢子菌病的首创孤儿产品。先前的研究表明,当在感染后 48 小时开始治疗时,它可以将致命的呼吸道感染降低到无法检测的水平。本研究使用已建立的小鼠呼吸道感染模型,重点研究 NikZ 剂量的第 2 阶段和第 3 阶段临床试验,感染后 120 小时开始治疗。每天 80 毫克/千克,分为 2 次剂量,几乎可以消除感染,而更大的剂量并不能提高真菌清除率。将治疗时间从 1 周延长至 3 周,可使更多的小鼠培养呈阴性。比较数据表明,在小鼠中几乎能消除新型隐球菌的 NikZ 血浆水平在患者中是可以达到的,为初始 2 期临床试验提供了一个合理的有效剂量范围。