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
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved 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 evidenceClinical
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 measuredDihydrofolate 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 measuredOther 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.
- FurazolidoneExisting use: Other antiinfectives and antiseptics91.4% AI-predicted activityagainst M. tuberculosisLab records exist49 registered studies
- TriflupromazineExisting use: Psychosis90.6% AI-predicted activityagainst M. tuberculosisNo documented evidence found
- ValdecoxibExisting use: Dysmenorrhea, Osteoarthritis, Rheumatic disease and 1 more88.6% AI-predicted activityagainst M. tuberculosisLab records exist31 registered studies
- CelecoxibExisting use: Ankylosing spondylitis, Cancer, Colorectal neoplasm and 15 more87.6% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
- Dorzolamide HydrochlorideExisting use: Glaucoma, Ocular hypertension, Open-angle glaucoma86.8% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
- MethazolamideExisting use: Glaucoma, Open-angle glaucoma85.6% AI-predicted activityagainst M. tuberculosisLab records exist11 registered studies
- AcetazolamideExisting use: Altitude sickness, Angle-closure glaucoma, Congestive heart failure and 5 more85.2% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
- Trifluoperazine HydrochlorideExisting use: Anxiety disorder, Mental or behavioural disorder, Psychosis and 1 more84.6% AI-predicted activityagainst M. tuberculosis1 registered study
- TriclosanExisting use: Phenol and derivatives, Medicated dressings with antiinfectives84.2% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
- NitrofurazoneExisting use: Eye infection, Leishmaniasis, Trypanosomiasis84.0% AI-predicted activityagainst M. tuberculosis8 registered studies
- BrinzolamideExisting use: Glaucoma, Ocular hypertension, Open-angle glaucoma83.8% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
- ZonisamideExisting use: Epilepsy, Focal-onset seizure, Partial epilepsy and 1 more82.8% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
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 NeutropeniaInterventionPiperacillin and Tazobactam for Injection; Cefepime Injection; Ceftazidime Injection; Vancomycin Injection +8 morePhasePhase 4Registry statusCompletedEffect 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 InfectionInterventionVancomycinPhasePhase 4Registry statusUnknownEvaluating 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 UlcerInterventionvancomycin-tobramycin-itraconazolePhaseEarly phase 1Registry statusUnknownSuprafascial 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 InfectionInterventionVancomycinPhasePhase 2Registry statusCompletedVancomycin 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.
ConditionOsteoarthritisInterventionPovidone iodine; Vancomycin powder; ConventionalPhasePhase 1Registry statusCompletedPharmacokinetic 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 InfectionInterventionBlood and microdialysis samplesPhasePhase 1Registry statusCompletedImpact 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 AdmissionInterventionNot recordedPhaseNot recordedRegistry statusUnknownA 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 ColitisInterventionVancomycin Pre-Treatment; Placebo for Vancomycin Pre-Treatment; SER-287; Placebo for SER-287PhasePhase 2Registry statusTerminatedVancomycin 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 PeritonitisInterventionVancomycinPhasePhase 1Registry statusCompletedEffect 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; SepsisInterventionVancomycin Continuous infusion; Vancomycin Intermittent infusionPhasePhase 4Registry statusUnknownAntibiotic 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 ProphylaxisInterventionCefazolinPhasePhase 4Registry statusCompletedOral 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 InfectionInterventionOral Vancomycin; PlaceboPhasePhase 4Registry statusTerminatedScreening 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 InfectionInterventionVancomycin; PlaceboPhasePhase 4Registry statusCompletedFMT 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 OrganismInterventionFecal Microbiota Transplant (FMT); Bowel preparation; Stool or perirectal swab sampling; FastingPhasePhase 1Registry statusTerminatedIntestinal 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 DifficileInterventionIntestinal Lavage; Vancomycin; PEG; MetronidazolePhasePhase 2 / Phase 3Registry statusUnknown