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

Expert Rev Anti Infect Ther

Department of Health Sciences (DISSAL), University of Genoa, Genoa, Italy.

Published: November 2024

AI Article Synopsis

  • Several new drugs are in advanced clinical trials aimed at treating resistant Gram-negative bacteria, which are difficult to treat with current antibiotics.
  • The review highlights agents that have either completed or are currently in phase-3 trials, focusing on research up to May 2024.
  • The novel agents, mainly β-lactams and β-lactam/β-lactamase inhibitors, show effectiveness against certain resistant strains, but most of their efficacy has been tested against bacteria that are still susceptible, making real-world studies important for future treatment guidelines.

Article Abstract

Introduction: Several 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 Covered: This review focuses on agents that have completed or ongoing phase-3 studies. A PubMed search was conducted up to 31 May 2024.

Expert Opinion: Novel agents in late-stage clinical development belong to the β-lactam or β-lactam/β-lactamase inhibitor combinations class and display variable antimicrobial activity depending on the specific β-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.

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Source
http://dx.doi.org/10.1080/14787210.2024.2407068DOI Listing

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