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Vancomycin 1.1%

Kurobe LLC · Phase 3 active Small molecule

Vancomycin inhibits cell wall synthesis in Gram-positive bacteria by binding to the D-alanyl-D-alanine terminus of cell wall precursors.

Vancomycin inhibits cell wall synthesis in Gram-positive bacteria by binding to the D-alanyl-D-alanine terminus of cell wall precursors. Used for Treatment of serious or severe bacterial infections caused by susceptible strains of methicillin-susceptible Staphylococcus aureus (MSSA), methicillin-resistant Staphylococcus aureus (MRSA), and other susceptible Gram-positive bacteria..

At a glance

Generic nameVancomycin 1.1%
SponsorKurobe LLC
Drug classglycopeptide antibiotic
TargetD-alanyl-D-alanine terminus of cell wall precursors
ModalitySmall molecule
Therapeutic areaInfectious Disease
PhasePhase 3

Mechanism of action

This prevents the incorporation of these precursors into the bacterial cell wall, ultimately leading to cell lysis and death. Vancomycin has a high affinity for the bacterial cell wall and is able to inhibit cell wall synthesis even at low concentrations.

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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