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January 26, 2026Current Infectious Disease Reports4 citationsOpen Access

Filling the Gaps: A Review and Update on Beta-Lactamase Inhibitor Combinations

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CJCourtney JacksonJWJohn WilliamsonJSJordan R. Smith

Key Points

  • This review aims to update on the efficacy and characteristics of novel beta-lactam/beta-lactamase inhibitor combinations against resistant pathogens.
  • Reviewed pharmacologic characteristics of newly approved beta-lactam/beta-lactamase inhibitor combinations.
  • Analyzed clinical efficacy data of Xacduro, Exblifep, and Emblaveo.
  • Discussed pipeline agents like cefepime/taniborbactam.
  • New agents like Xacduro and Exblifep have received FDA approval.
  • Promising combinations show potential in treating multidrug-resistant infections.
  • The ongoing development of these agents addresses significant treatment gaps.

Abstract

Abstract Purpose of Review Gram-negative antimicrobial resistance continues to pose a growing threat, particularly among high-priority pathogens such as difficult-to-treat Pseudomonas aeruginosa , carbapenem-resistant Acinetobacter baumannii (CRAB), and carbapenem-resistant Enterobacterales (CRE). The rise in resistance has spurred the development of novel beta-lactam/beta-lactamase inhibitor (BL/BLI) combinations. However, the pace of innovation has lagged behind the rapid emergence of resistance, especially for CRAB and metallo-beta-lactamase (MBL)-producing Enterobacterales, organisms for which effective treatment options have been historically limited. This review outlines the pharmacologic characteristics, activity, and clinical efficacy data for newly approved BL/BLIs Recent Findings The FDA has recently approved Xacduro (sulbactam/durlobactam), Exblifep (cefepime/enmetazobactam), and Emblaveo (aztreonam/avibactam). Additionally, promising pipeline agents such as cefepime/taniborbactam, cefepime/zidebactam, and imipenem/cilastatin/funobactam warrant discussion. These agents offer significant potential to fill longstanding therapeutic gaps. Summary As resistance mechanisms evolve and therapeutic challenges persist, development of novel BL/BLIs will play an increasingly critical role in the management of multidrug-resistant gram-negative infections.

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Cite This Study

Jackson et al. (2026) studied this question.

synapsesocial.com/papers/697703d3722626c4468e8d41https://doi.org/10.1007/s11908-025-00874-y
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