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Vancomycin intermittent dosing interval

Massachusetts General Hospital · FDA-approved active Small molecule

Vancomycin is a glycopeptide antibiotic that inhibits bacterial cell wall synthesis by binding to D-Ala-D-Ala peptidoglycan precursors.

Vancomycin is a glycopeptide antibiotic that inhibits bacterial cell wall synthesis by binding to D-Ala-D-Ala peptidoglycan precursors. Used for Serious gram-positive bacterial infections including methicillin-resistant Staphylococcus aureus (MRSA), Clostridium difficile-associated diarrhea, Endocarditis.

At a glance

Generic nameVancomycin intermittent dosing interval
SponsorMassachusetts General Hospital
Drug classGlycopeptide antibiotic
TargetBacterial peptidoglycan (D-Ala-D-Ala)
ModalitySmall molecule
Therapeutic areaInfectious Disease
PhaseFDA-approved

Mechanism of action

Vancomycin works by preventing cross-linking of peptidoglycan strands in the bacterial cell wall, leading to cell wall instability and bacterial death. The intermittent dosing interval refers to the clinical dosing schedule (typically every 8-12 hours) rather than a novel mechanism, optimizing drug exposure and reducing nephrotoxicity while maintaining efficacy against susceptible gram-positive organisms.

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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