» Articles » PMID: 32060929

Imipenem-Cilastatin-Relebactam: A Novel β-Lactam-β-Lactamase Inhibitor Combination for the Treatment of Multidrug-Resistant Gram-Negative Infections

Overview
Journal Pharmacotherapy
Specialty Pharmacology
Date 2020 Feb 16
PMID 32060929
Citations 27
Authors
Affiliations
Soon will be listed here.
Abstract

Imipenem-cilastatin-relebactam (IMI-REL) is a novel β-lactam-β-lactamase inhibitor combination recently approved for the treatment of complicated urinary tract infections (cUTIs) and complicated intraabdominal infections (cIAIs). Relebactam is a β-lactamase inhibitor with the ability to inhibit a broad spectrum of β-lactamases such as class A and class C β-lactamases, including carbapenemases. The addition of relebactam to imipenem restores imipenem activity against several imipenem-resistant bacteria, including Enterobacteriaceae and Pseudomonas aeruginosa. Clinical data demonstrate that IMI-REL is well tolerated and effective in the treatment of cUTIs and cIAIs due to imipenem-resistant bacteria. In a phase III trial comparing IMI-REL with imipenem plus colistin, favorable clinical response was achieved in 71% and 70% of patients, respectively. Available clinical and pharmacokinetic data support the approved dosage of a 30-minute infusion of imipenem 500 mg-cilastatin 500 mg-relebactam 250 mg every 6 hours, along with dosage adjustments based on renal function. In this review, we describe the chemistry, mechanism of action, spectrum of activity, pharmacokinetics and pharmacodynamics, and clinical efficacy, and safety and tolerability of this new agent. The approval of IMI-REL represents another important step in the ongoing fight against multidrug-resistant gram-negative pathogens.

Citing Articles

Evaluation of multidrug resistance in the Gram-negative microbiome of cancer patients and the adverse effects of their metabolites on albino rats and epithelial or fibroblasts cell lines.

El-Gendy M, Alghamdi H, Abdel-Wahhab K, Hassan N, El-Bondkly A, Abdel-Wahab M Infect Agent Cancer. 2025; 20(1):2.

PMID: 39819472 PMC: 11740417. DOI: 10.1186/s13027-024-00634-y.


In Vitro Dynamic Model Evaluation of Meropenem Alone and in Combination with Avibactam Against Carbapenemase-Producing .

Strukova E, Portnoy Y, Golikova M, Zinner S Pharmaceuticals (Basel). 2025; 17(12.

PMID: 39770525 PMC: 11678027. DOI: 10.3390/ph17121683.


Real-world use of imipenem/cilastatin/relebactam for the treatment of KPC-producing complex and difficult-to-treat resistance (DTR) infections: a single-center preliminary experience.

Leanza C, Mascellino M, Volpicelli L, Covino S, Falletta A, Cancelli F Front Microbiol. 2024; 15:1432296.

PMID: 39081883 PMC: 11286388. DOI: 10.3389/fmicb.2024.1432296.


Phenotypic and Genotypic Characterization of Pan-Drug-Resistant Isolated in Qatar.

Ahmed M, Hamid J, Hassan A, Abu Jarir S, Ibrahim E, Hadi H Antibiotics (Basel). 2024; 13(3).

PMID: 38534710 PMC: 10967633. DOI: 10.3390/antibiotics13030275.


Role of β-Lactamase Inhibitors as Potentiators in Antimicrobial Chemotherapy Targeting Gram-Negative Bacteria.

Zhang S, Liao X, Ding T, Ahn J Antibiotics (Basel). 2024; 13(3).

PMID: 38534695 PMC: 10967447. DOI: 10.3390/antibiotics13030260.