Pharmacodynamics of the Novel Metallo-β-Lactamase Inhibitor ANT2681 in Combination with Meropenem for the Treatment of Infections Caused by NDM-Producing Enterobacteriaceae

Author:

Das Shampa1ORCID,Johnson Adam1,McEntee Laura1,Farrington Nicola1,Kirby Adam1,Unsworth Jennifer1,Jimenez-Valverde Ana1,Kolamunnage-Dona Ruwanthi2,Bousquet Justine3,Alibaud Laethitia3,Sable Carole3,Zalacain Magdalena3,Everett Martin3ORCID,Hope William1ORCID

Affiliation:

1. Antimicrobial Pharmacodynamics and Therapeutics, University of Liverpool, Liverpool Health Partners, Liverpool, United Kingdom

2. Department of Biostatistics, University of Liverpool, Liverpool Health Partners, Liverpool, United Kingdom

3. Antabio SAS, Labège, France

Abstract

Enterobacteriaceae that produce metallo-β-lactamases (MBLs) are an emerging threat to public health. The metallo-β-lactamase inhibitor (MBLi) ANT2681 inhibits the enzymatic activity of MBLs through interaction with the dinuclear zinc ion cluster present in the active site that is common to these enzymes. ANT2681 is being codeveloped, with meropenem as the partner β-lactam, as a novel combination therapy for infections caused by MBL-producing bacteria. The pharmacokinetics/pharmacodynamics of meropenem-ANT2681 were studied in a murine neutropenic thigh model of NDM-producing Enterobacteriaceae .

Funder

Antabio

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

Reference30 articles.

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