Novel agents in development for the treatment of resistant Gram-negative infections

被引:1
|
作者
Bassetti, Matteo [1 ,2 ]
Larosa, Barbara [1 ]
Vena, Antonio [1 ,2 ]
Giacobbe, Daniele Roberto [1 ,2 ]
机构
[1] Univ Genoa, Dept Hlth Sci DISSAL, Genoa, Italy
[2] IRCCS Osped Policlin San Martino, UO Clin Malattie Infett, L Go R Benzi 10, I-16132 Genoa, Italy
关键词
Aztreonam/avibactam; aztreonam/nacubactam; cefepime/enmetazobactam; cefepime/nacubactam; cefepime/taniborbactam; cefepime/tazobactam; cefepime/zidebactam; durlobactam/sulbactam; imipenem/cilastatin/funobactam; tebipenem; BETA-LACTAMASE INHIBITOR; IN-VIVO ACTIVITIES; VITRO ACTIVITY; ANTIMICROBIAL ACTIVITY; EXTENDED-SPECTRUM; WCK; 5222; CEFEPIME; COMBINATION; DIAZABICYCLOOCTANE; OP0595;
D O I
10.1080/14787210.2024.2407068
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
IntroductionSeveral novel agents are in advanced stages of clinical development, potentially expanding our treatment options against third- and fourth-generation cephalosporin-resistant and carbapenem-resistant Gram-negative bacteria (GNB), including those pathogens for which the current number of effective treatments is limited.Areas coveredThis review focuses on agents that have completed or ongoing phase-3 studies. A PubMed search was conducted up to 31 May 2024.Expert opinionNovel agents in late-stage clinical development belong to the beta-lactam or beta-lactam/beta-lactamase inhibitor combinations class and display variable antimicrobial activity depending on the specific beta-lactamases expressed by GNB, particularly carbapenemases. While many of these novel agents demonstrate in vitro activity against carbapenem-resistant GNB, their efficacy has mainly been evaluated in phase-3 randomized controlled trials (RCT) for infections caused by carbapenem-susceptible GNB. Although evidence from real-world observational studies is generally less robust than that from RCT, it could be crucial for updating clinical guidelines on treating carbapenem-resistant GNB with these new agents in the absence of dedicated RCT.
引用
收藏
页码:965 / 976
页数:12
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