Drug intelligence / Profile preview

cefepime + ertapenem + vancomycin

Development stage
Unknown
Lead developer
Bristol Myers Squibb
Modality
Peptides, Small Molecules
Administration
Intravenous
01

Overview

This is a combination of three intravenous antibiotics—cefepime, ertapenem, and vancomycin—used together for the empiric or targeted treatment of severe or resistant bacterial infections. - **Cefepime** is a fourth-generation cephalosporin with broad-spectrum activity against Gram-positive and Gram-negative bacteria, including *Pseudomonas aeruginosa*. It is stable against many beta-lactamases and often used in hospital-acquired infections[4][1]. - **Ertapenem** is a carbapenem antibiotic effective against many Gram-positive and Gram-negative organisms (including ESBL producers), but notably lacks activity against *Pseudomonas* and *Acinetobacter*. Its main advantage is once-daily dosing[2][6]. - **Vancomycin** is a glycopeptide antibiotic primarily active against Gram-positive bacteria, especially methicillin-resistant *Staphylococcus aureus* (MRSA) and other resistant staphylococci. It inhibits cell wall synthesis by binding to D-Ala-D-Ala termini of peptidoglycan precursors. The combination may be used in critically ill patients when broad-spectrum coverage—including MRSA, ESBL-producing Enterobacteriaceae, anaerobes, and other multidrug-resistant organisms—is required before pathogen identification or susceptibility results are available. This regimen provides overlapping but complementary mechanisms targeting cell wall synthesis at different sites.

02

Targets

PBP3 (Peptidoglycan D,D-transpeptidase FtsI)D-Ala-D-Ala (D-Ala-D-Ala terminus)

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