Skip to content

Vancomycin

FDA-approved product (solution, intravenous, oral), marketed as Vancomycin, Firvanq Kit, Tyzavan and 5 more.

Registered studies
50+
Lab records
118
Pathogens at ≥40%
3 of 4

Chemical structure

Chemical structure of Vancomycin
A drawing shows what the molecule is, not what it does.

Existing / approved use

Documented · FDA, WHO, ChEMBL

Approved for

  • Bacterial disease
  • Diarrhea
  • Endocarditis
  • Enterocolitis
  • Eye infection
  • Infection
  • Infective endocarditis
  • Respiratory tract infectious disorder
  • Sepsis
  • Skin disease
  • Skin infection

Indications ChEMBL records as approved, from FDA and DailyMed labels. Label ↗

WHO therapeutic group
Antibiotics; Glycopeptide antibacterials
Anti-infective classification
Classified as an existing antimicrobial.WHO ATC J01XA01; WHO ATC A07AA09; WHO ATC S01AA28

Repurposing investigation

Vancomycin is already an antimicrobial, so it is not counted among the repurposing candidates. Its AI-predicted activity is shown below for reference.

AI-predicted activity

AI prediction · nothing measured
  • MRSA>99% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates. This medicine was in the model's training data, so this is recall, not a new prediction.
  • E. coli78.1% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates. This medicine was in the model's training data, so this is recall, not a new prediction.
  • K. pneumoniae80.6% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates. This medicine was in the model's training data, so this is recall, not a new prediction.
  • M. tuberculosis14.4% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates. This medicine was in the model's training data, so this is recall, not a new prediction.

A model’s estimate of laboratory activity against each pathogen species. It is not clinical effectiveness.

Evidence

Clinical and experimental

Documented evidence

Clinical

50+registered studies name this medicine, for any condition. The registry search keeps the first 50, so there may be more. See them below.

Experimental

  • MRSA: measured active in 103 of 103 lab records
  • E. coli: measured active in 8 of 9 lab records
  • K. pneumoniae: measured active in 2 of 3 lab records
  • M. tuberculosis: measured active in 0 of 3 lab records
Show the 118 laboratory records, with sources

Loading records…

“Active” means the measured value reached this project’s laboratory cutoff (10 µM or stronger). A laboratory result does not show an effect in patients.

Docking

Computational · nothing measured

Dihydrofolate reductase ↗ (E. coli)

Not yet docked: queued in the docking rundetails

KPC-2 carbapenemase ↗ (K. pneumoniae)

Not yet docked: queued in the docking rundetails

Enoyl-ACP reductase (InhA) ↗ (M. tuberculosis)

Not yet docked: queued in the docking rundetails

Dihydrofolate reductase ↗ (MRSA)

Not yet docked: queued in the docking rundetails

AutoDock Vina, one experimentally solved protein per pathogen. This project’s screening target is -7.0 kcal/mol, its own mark rather than a universal cutoff. A docking score is a structural hypothesis, not proof of binding, and requires experimental validation.

Other medicines to investigate

AI prediction · nothing measured

Other repurposing candidates: approved medicines besides Vancomycin with AI-predicted activity ≥40% against the chosen pathogen, leaving out existing antimicrobials. They are computational candidates for further investigation, not alternatives and not recommendations.

Sorted by AI-predicted activity, high to low. The order is not a ranking of which medicine is better.

Registered studies

A registration describes a study; it does not establish a positive result.

  • Early Versus Late Stopping of Antibiotics in Children With Cancer and High-risk Febrile Neutropenia

    NCT04948463 · start 2021-11-15

    Registered record
    Registry ID
    NCT04948463
    Conditions
    Febrile Neutropenia
    Interventions
    Piperacillin and Tazobactam for Injection; Cefepime Injection; Ceftazidime Injection; Vancomycin Injection; Amikacin Injection; Ciprofloxacin; Piperacillin and Tazobactam for Injection; Cefepime Injection; Ceftazidime Injection; Vancomycin Injection; Amikacin Injection; Ciprofloxacin
    Study type
    INTERVENTIONAL
    Phase
    Phase 4
    Registry status
    Completed
    Start
    2021-11-15
    Completion
    2025-12-17
    Enrolment
    55

    As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.

    ConditionFebrile Neutropenia
    InterventionPiperacillin and Tazobactam for Injection; Cefepime Injection; Ceftazidime Injection; Vancomycin Injection +8 more
    PhasePhase 4
    Registry statusCompleted
  • Effect of Vancomycin After Catheter Replacement

    NCT04856878 · start 2021-06-01

    Registered record
    Registry ID
    NCT04856878
    Conditions
    Central Line-associated Bloodstream Infection (CLABSI); Catheter-related Bloodstream Infection
    Interventions
    Vancomycin
    Study type
    INTERVENTIONAL
    Phase
    Phase 4
    Registry status
    Unknown
    Start
    2021-06-01
    Completion
    2024-12-31
    Enrolment
    100

    As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.

    ConditionCentral Line-associated Bloodstream Infection (CLABSI); Catheter-related Bloodstream Infection
    InterventionVancomycin
    PhasePhase 4
    Registry statusUnknown
  • Evaluating the Healing of Diabetic Foot Ulcers With Compounded Anti-Infective Irrigation Therapy

    NCT05076955 · start 2021-03-31

    Registered record
    Registry ID
    NCT05076955
    Conditions
    Diabetic Foot Ulcer
    Interventions
    vancomycin-tobramycin-itraconazole
    Study type
    INTERVENTIONAL
    Phase
    Early phase 1
    Registry status
    Unknown
    Start
    2021-03-31
    Completion
    2022-12
    Enrolment
    100

    As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.

    ConditionDiabetic Foot Ulcer
    Interventionvancomycin-tobramycin-itraconazole
    PhaseEarly phase 1
    Registry statusUnknown
  • Suprafascial Vancomycin Powder for Prevention of Surgical Site Infections After Instrumented Posterior Spinal Fusion

    NCT04017468 · start 2019-10-15

    Registered record
    Registry ID
    NCT04017468
    Conditions
    Surgical Site Infection
    Interventions
    Vancomycin
    Study type
    INTERVENTIONAL
    Phase
    Phase 2
    Registry status
    Completed
    Start
    2019-10-15
    Completion
    2026-07-31
    Enrolment
    450

    As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.

    ConditionSurgical Site Infection
    InterventionVancomycin
    PhasePhase 2
    Registry statusCompleted
  • Vancomycin Powder and Dilute Povidone Iodine Lavage for Infection Prophylaxis in High Risk Total Joint Arthroplasty

    NCT04075526 · start 2019-10-01

    Registered record
    Registry ID
    NCT04075526
    Conditions
    Osteoarthritis
    Interventions
    Povidone iodine; Vancomycin powder; Conventional
    Study type
    INTERVENTIONAL
    Phase
    Phase 1
    Registry status
    Completed
    Start
    2019-10-01
    Completion
    2025-12-13
    Enrolment
    2,129

    As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.

    ConditionOsteoarthritis
    InterventionPovidone iodine; Vancomycin powder; Conventional
    PhasePhase 1
    Registry statusCompleted
  • Pharmacokinetic Study of Vancomycin, Clindamycin And/or Gentamicin Administration During Surgery Using a Microdialysis Procedure

    NCT03845790 · start 2019-05-26

    Registered record
    Registry ID
    NCT03845790
    Conditions
    Surgical Site Infection
    Interventions
    Blood and microdialysis samples
    Study type
    INTERVENTIONAL
    Phase
    Phase 1
    Registry status
    Completed
    Start
    2019-05-26
    Completion
    2024-09-04
    Enrolment
    25

    As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.

    ConditionSurgical Site Infection
    InterventionBlood and microdialysis samples
    PhasePhase 1
    Registry statusCompleted
  • Impact of Prescription Quality, Infection Control and Antimicrobial Stewardship on Gut Microbiota Domination by Healthcare-Associated Pathogens

    NCT03765528 · start 2019-01-01

    Registered record
    Registry ID
    NCT03765528
    Conditions
    Patients at High Risk of Antibacterial Treatment Upon Admission
    Interventions
    Not recorded
    Study type
    OBSERVATIONAL
    Phase
    Not recorded
    Registry status
    Unknown
    Start
    2019-01-01
    Completion
    2022-07-31
    Enrolment
    1,500

    As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.

    ConditionPatients at High Risk of Antibacterial Treatment Upon Admission
    InterventionNot recorded
    PhaseNot recorded
    Registry statusUnknown
  • A Study to Assess Efficacy and Safety of SER-287 in Adults With Active Mild-to-Moderate Ulcerative Colitis

    NCT03759041 · start 2018-12-19

    Registered record
    Registry ID
    NCT03759041
    Conditions
    Ulcerative Colitis
    Interventions
    Vancomycin Pre-Treatment; Placebo for Vancomycin Pre-Treatment; SER-287; Placebo for SER-287
    Study type
    INTERVENTIONAL
    Phase
    Phase 2
    Registry status
    Terminated
    Start
    2018-12-19
    Completion
    2021-10-13
    Enrolment
    203

    As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.

    ConditionUlcerative Colitis
    InterventionVancomycin Pre-Treatment; Placebo for Vancomycin Pre-Treatment; SER-287; Placebo for SER-287
    PhasePhase 2
    Registry statusTerminated
  • Vancomycin Pharmacokinetics in Patients on Peritoneal Dialysis

    NCT03685747 · start 2018-11-15

    Registered record
    Registry ID
    NCT03685747
    Conditions
    Peritoneal Dialysis-associated Peritonitis
    Interventions
    Vancomycin
    Study type
    INTERVENTIONAL
    Phase
    Phase 1
    Registry status
    Completed
    Start
    2018-11-15
    Completion
    2020-10-01
    Enrolment
    4

    As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.

    ConditionPeritoneal Dialysis-associated Peritonitis
    InterventionVancomycin
    PhasePhase 1
    Registry statusCompleted
  • Effect of Intermittent Infusion Versus Continuous Infusion of Vancomycin on Kidney Failure in Critically Ill Patients

    NCT03438214 · start 2018-04-28

    Registered record
    Registry ID
    NCT03438214
    Conditions
    Gram-Positive Bacterial Infections; Nephrotoxicity; Sepsis
    Interventions
    Vancomycin Continuous infusion; Vancomycin Intermittent infusion
    Study type
    INTERVENTIONAL
    Phase
    Phase 4
    Registry status
    Unknown
    Start
    2018-04-28
    Completion
    2022-12-01
    Enrolment
    222

    As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.

    ConditionGram-Positive Bacterial Infections; Nephrotoxicity; Sepsis
    InterventionVancomycin Continuous infusion; Vancomycin Intermittent infusion
    PhasePhase 4
    Registry statusUnknown
  • Antibiotic Prophylaxis in Patients Undergoing Elective Total Knee Arthroplasty- Multi-center Trial

    NCT03283878 · start 2017-10-24

    Registered record
    Registry ID
    NCT03283878
    Conditions
    Arthropathy of Knee; Antibiotic Prophylaxis
    Interventions
    Cefazolin
    Study type
    INTERVENTIONAL
    Phase
    Phase 4
    Registry status
    Completed
    Start
    2017-10-24
    Completion
    2025-08-22
    Enrolment
    1,770

    As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.

    ConditionArthropathy of Knee; Antibiotic Prophylaxis
    InterventionCefazolin
    PhasePhase 4
    Registry statusCompleted
  • Oral Vancomycin for Preventing Clostridium Difficile Recurrence

    NCT03200093 · start 2017-06-08

    Registered record
    Registry ID
    NCT03200093
    Conditions
    Clostridium Difficile Infection
    Interventions
    Oral Vancomycin; Placebo
    Study type
    INTERVENTIONAL
    Phase
    Phase 4
    Registry status
    Terminated
    Start
    2017-06-08
    Completion
    2021-04-22
    Enrolment
    65

    As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.

    ConditionClostridium Difficile Infection
    InterventionOral Vancomycin; Placebo
    PhasePhase 4
    Registry statusTerminated
  • Screening to Prophylax Against Clostridium Difficile Infection -

    NCT02996487 · start 2016-12-19

    Registered record
    Registry ID
    NCT02996487
    Conditions
    Clostridium Difficile Infection
    Interventions
    Vancomycin; Placebo
    Study type
    INTERVENTIONAL
    Phase
    Phase 4
    Registry status
    Completed
    Start
    2016-12-19
    Completion
    2023-06-28
    Enrolment
    1,294

    As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.

    ConditionClostridium Difficile Infection
    InterventionVancomycin; Placebo
    PhasePhase 4
    Registry statusCompleted
  • FMT for MDRO Colonization After Infection in Renal Transplant Recipients

    NCT02922816 · start 2016-12-01

    Registered record
    Registry ID
    NCT02922816
    Conditions
    Infection Due to Resistant Organism
    Interventions
    Fecal Microbiota Transplant (FMT); Bowel preparation; Stool or perirectal swab sampling; Fasting
    Study type
    INTERVENTIONAL
    Phase
    Phase 1
    Registry status
    Terminated
    Start
    2016-12-01
    Completion
    2021-12-03
    Enrolment
    11

    As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.

    ConditionInfection Due to Resistant Organism
    InterventionFecal Microbiota Transplant (FMT); Bowel preparation; Stool or perirectal swab sampling; Fasting
    PhasePhase 1
    Registry statusTerminated
  • Intestinal Lavage for the Treatment of Severe C. Difficile Infections

    NCT02466698 · start 2016-08

    Registered record
    Registry ID
    NCT02466698
    Conditions
    Clostridium Difficile
    Interventions
    Intestinal Lavage; Vancomycin; PEG; Metronidazole
    Study type
    INTERVENTIONAL
    Phase
    Phase 2 / Phase 3
    Registry status
    Unknown
    Start
    2016-08
    Completion
    2019-08
    Enrolment
    20

    As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.

    ConditionClostridium Difficile
    InterventionIntestinal Lavage; Vancomycin; PEG; Metronidazole
    PhasePhase 2 / Phase 3
    Registry statusUnknown