Center for Anti-Infective Agents, Vienna, Austria.
Biovision Foundation for Ecological Development, Zurich, Switzerland.
Lancet Infect Dis. 2019 Feb;19(2):e40-e50. doi: 10.1016/S1473-3099(18)30513-9. Epub 2018 Oct 15.
This analysis of the global clinical antibacterial pipeline was done in support of the Global Action Plan on Antimicrobial Resistance. The study analysed to what extent antibacterial and antimycobacterial drugs for systemic human use as well as oral non-systemic antibacterial drugs for Clostridium difficile infections were active against pathogens included in the WHO priority pathogen list and their innovativeness measured by their absence of cross-resistance (new class, target, mode of action). As of July 1, 2018, 30 new chemical entity (NCE) antibacterial drugs, ten biologics, ten NCEs against Mycobacterium tuberculosis, and four NCEs against C difficile were identified. Of the 30 NCEs, 11 are expected to have some activity against at least one critical priority pathogen expressing carbapenem resistance. The clinical pipeline is dominated by derivatives of established classes and most development candidates display limited innovation. New antibacterial drugs without pre-existing cross-resistance are under-represented and are urgently needed, especially for geographical regions with high resistance rates among Gram-negative bacteria and M tuberculosis.
本分析全球临床抗菌药物管道是在支持全球行动计划对抗菌药物耐药性。该研究分析了在何种程度上抗菌和抗分枝杆菌药物全身人类使用以及口服非全身抗菌药物艰难梭菌感染是针对病原体的活性包括在世界卫生组织优先病原体清单和他们的创新性通过他们缺乏交叉耐药性(新的类别,目标,作用模式)。截至 2018 年 7 月 1 日,确定了 30 种新的化学实体(NCE)抗菌药物、10 种生物制品、10 种针对结核分枝杆菌的 NCE 和 4 种针对艰难梭菌的 NCE。在这 30 种 NCE 中,预计有 11 种对至少一种表达碳青霉烯类耐药的关键优先病原体具有一定的活性。临床管道主要由已建立的类别衍生而来,大多数开发候选药物显示出有限的创新性。没有预先存在的交叉耐药性的新抗菌药物代表性不足,迫切需要,特别是在革兰氏阴性菌和 M 结核分枝杆菌耐药率高的地区。