Drug intelligence / Profile preview

cefoperazone + sulbactam + tigecycline

Development stage
Preclinical
Lead developer
Pfizer
Modality
Small Molecules
Administration
Intravenous
01

Overview

This is a combination of three antibiotics—cefoperazone, sulbactam, and tigecycline—used primarily for the treatment of severe infections caused by multidrug-resistant (MDR) bacteria, especially Acinetobacter baumannii. Cefoperazone is a third-generation cephalosporin that inhibits bacterial cell wall synthesis by binding to penicillin-binding proteins. Sulbactam is a β-lactamase inhibitor that extends the spectrum of cefoperazone by inhibiting β-lactamases produced by resistant bacteria. Tigecycline is a glycylcycline antibiotic that binds to the 30S ribosomal subunit and inhibits protein synthesis in susceptible organisms. The combination has demonstrated synergistic or additive effects in vitro and in clinical studies against MDR pathogens, particularly when resistance to individual agents limits their efficacy alone[1][3][8]. This regimen is considered for critically ill patients with limited therapeutic options due to extensive drug resistance.

Other names
cefoperazone-sulbactam-tigecycline combinationcefoperazone/sulbactam/tigecycline
02

Targets

PBP (Penicillin-binding protein family)30S A-site (Bacterial ribosomal 30S A-site)β-lactamase

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