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Vancomycin - model-based dosing regimen

Murdoch Childrens Research Institute · FDA-approved active Small molecule

Vancomycin inhibits bacterial cell wall synthesis by binding to D-Ala-D-Ala peptidoglycan precursors, preventing cross-linking and causing cell wall disruption.

Vancomycin inhibits bacterial cell wall synthesis by binding to D-Ala-D-Ala peptidoglycan precursors, preventing cross-linking and causing cell wall disruption. Used for Serious infections caused by susceptible Gram-positive bacteria (including methicillin-resistant Staphylococcus aureus), Clostridium difficile-associated diarrhea, Endocarditis.

At a glance

Generic nameVancomycin - model-based dosing regimen
SponsorMurdoch Childrens Research Institute
Drug classGlycopeptide antibiotic
TargetD-Ala-D-Ala peptidoglycan precursor
ModalitySmall molecule
Therapeutic areaInfectious Disease
PhaseFDA-approved

Mechanism of action

Vancomycin is a glycopeptide antibiotic that binds to the D-alanyl-D-alanine terminus of peptidoglycan precursors in bacterial cell walls, blocking transglycosylation and transpeptidation reactions essential for cell wall integrity. This leads to cell wall weakening and bacterial cell lysis. The model-based dosing regimen optimizes pharmacokinetic/pharmacodynamic (PK/PD) parameters to achieve target drug exposures that maximize bacterial killing while minimizing toxicity.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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