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Administration of Vancomycin

University of Colorado, Denver · FDA-approved active Small molecule

Administration of Vancomycin is a Glycopeptide antibiotic Small molecule drug developed by University of Colorado, Denver. It is currently FDA-approved for Serious infections caused by susceptible strains of methicillin-resistant Staphylococcus aureus (MRSA), Clostridium difficile-associated diarrhea and colitis, Endocarditis caused by susceptible streptococci or staphylococci. Also known as: Vancomycin Hydrochloride.

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

Vancomycin inhibits bacterial cell wall synthesis by binding to D-Ala-D-Ala peptide precursors and preventing peptidoglycan cross-linking. Used for Serious infections caused by susceptible strains of methicillin-resistant Staphylococcus aureus (MRSA), Clostridium difficile-associated diarrhea and colitis, Endocarditis caused by susceptible streptococci or staphylococci.

At a glance

Generic nameAdministration of Vancomycin
Also known asVancomycin Hydrochloride
SponsorUniversity of Colorado, Denver
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 the cross-linking of peptidoglycan strands. This disrupts cell wall integrity and leads to bacterial cell lysis and death. It is bactericidal and particularly effective against 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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Frequently asked questions about Administration of Vancomycin

What is Administration of Vancomycin?

Administration of Vancomycin is a Glycopeptide antibiotic drug developed by University of Colorado, Denver, indicated for Serious infections caused by susceptible strains of methicillin-resistant Staphylococcus aureus (MRSA), Clostridium difficile-associated diarrhea and colitis, Endocarditis caused by susceptible streptococci or staphylococci.

How does Administration of Vancomycin work?

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

What is Administration of Vancomycin used for?

Administration of Vancomycin is indicated for Serious infections caused by susceptible strains of methicillin-resistant Staphylococcus aureus (MRSA), Clostridium difficile-associated diarrhea and colitis, Endocarditis caused by susceptible streptococci or staphylococci, Septicemia caused by susceptible gram-positive cocci.

Who makes Administration of Vancomycin?

Administration of Vancomycin is developed and marketed by University of Colorado, Denver (see full University of Colorado, Denver pipeline at /company/university-of-colorado-denver).

Is Administration of Vancomycin also known as anything else?

Administration of Vancomycin is also known as Vancomycin Hydrochloride.

What drug class is Administration of Vancomycin in?

Administration of Vancomycin belongs to the Glycopeptide antibiotic class. See all Glycopeptide antibiotic drugs at /class/glycopeptide-antibiotic.

What development phase is Administration of Vancomycin in?

Administration of Vancomycin is FDA-approved (marketed).

What are the side effects of Administration of Vancomycin?

Common side effects of Administration of Vancomycin include Nephrotoxicity, Ototoxicity, Red man syndrome (flushing, pruritus), Phlebitis at infusion site, Fever, Chills.

What does Administration of Vancomycin target?

Administration of Vancomycin targets D-Ala-D-Ala peptidoglycan precursor and is a Glycopeptide antibiotic.

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