MSBChem Consulting, Brisbane, Queensland, Australia.
Institute for Molecular Bioscience, University of Queensland, Brisbane, Queensland, Australia.
Antimicrob Agents Chemother. 2022 Mar 15;66(3):e0199121. doi: 10.1128/AAC.01991-21. Epub 2022 Jan 10.
There is an urgent global need for new strategies and drugs to control and treat multidrug-resistant bacterial infections. In 2017, the World Health Organization (WHO) released a list of 12 antibiotic-resistant priority pathogens and began to critically analyze the antibacterial clinical pipeline. This review analyzes "traditional" and "nontraditional" antibacterial agents and modulators in clinical development current on 30 June 2021 with activity against the WHO priority pathogens mycobacteria and Clostridioides difficile. Since 2017, 12 new antibacterial drugs have been approved globally, but only vaborbactam belongs to a new antibacterial class. Also innovative is the cephalosporin derivative cefiderocol, which incorporates an iron-chelating siderophore that facilitates Gram-negative bacteria cell entry. Overall, there were 76 antibacterial agents in clinical development (45 traditional and 31 nontraditional), with 28 in phase 1, 32 in phase 2, 12 in phase 3, and 4 under regulatory evaluation. Forty-one out of 76 (54%) targeted WHO priority pathogens, 16 (21%) were against mycobacteria, 15 (20%) were against C. difficile, and 4 (5%) were nontraditional agents with broad-spectrum effects. Nineteen of the 76 antibacterial agents have new pharmacophores, and 4 of these have new modes of actions not previously exploited by marketed antibacterial drugs. Despite there being 76 antibacterial clinical candidates, this analysis indicated that there were still relatively few clinically differentiated antibacterial agents in late-stage clinical development, especially against critical-priority pathogens. We believe that future antibacterial research and development (R&D) should focus on the development of innovative and clinically differentiated candidates that have clear and feasible progression pathways to the market.
全球急需新的策略和药物来控制和治疗耐多药细菌感染。2017 年,世界卫生组织(WHO)发布了 12 种抗药性优先病原体的清单,并开始对抗菌药物临床研发管道进行严格分析。本综述分析了截至 2021 年 6 月 30 日针对 WHO 优先病原体分枝杆菌和艰难梭菌具有活性的临床开发中的“传统”和“非传统”抗菌药物和调节剂。自 2017 年以来,全球已批准了 12 种新的抗菌药物,但只有沃博巴坦属于新的抗菌类别。具有创新性的还有头孢菌素衍生物头孢地尔,它结合了一种铁螯合的铁载体,有助于革兰氏阴性菌细胞进入。总体而言,有 76 种抗菌药物正在临床开发中(45 种为传统药物,31 种为非传统药物),其中 28 种处于 1 期,32 种处于 2 期,12 种处于 3 期,4 种处于监管评估中。76 种抗菌药物中有 41 种(54%)针对 WHO 优先病原体,16 种(21%)针对分枝杆菌,15 种(20%)针对艰难梭菌,4 种(5%)是非传统的广谱作用药物。76 种抗菌药物中有 19 种具有新的药效团,其中 4 种具有以前未被市场抗菌药物利用的新作用模式。尽管有 76 种抗菌临床候选药物,但本分析表明,处于后期临床开发阶段的具有临床差异化的抗菌药物相对较少,尤其是针对关键优先病原体的药物。我们认为,未来的抗菌药物研发(R&D)应侧重于开发具有创新性和临床差异化的候选药物,这些候选药物具有明确且可行的市场推广途径。