Voriconazole
FDA-approved product (tablet, oral), marketed as Vfend, Voriconazole.
- Registered studies
- 50+
- Lab records
- 0
- Pathogens at ≥40%
- 2 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Aspergillosis
- Bacterial Infections and Mycoses
- Candidemia
- Candidiasis
- Fungal infectious disease
- Fusariosis
- Infection
Indications ChEMBL records as approved, from FDA and DailyMed labels. Label ↗
- WHO therapeutic group
- Triazole and tetrazole derivatives
- FDA pharmacologic class
- Azole Antifungal FDA label ↗
- Anti-infective classification
- Classified as another kind of anti-infective (for example an antifungal, antiviral or antiparasitic medicine).WHO ATC J02AC03; FDA class Azole Antifungal
Repurposing investigation
This medicine is being investigated here for AI-predicted antimicrobial activity against MRSA and M. tuberculosis. It was surfaced computationally for further investigation; it is not an established treatment for these infections.
AI-predicted activity
AI prediction · nothing measured- MRSA52.1% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- E. coli36.4% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- K. pneumoniae20.8% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- M. tuberculosis49.8% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
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
No evidence found
No laboratory measurement against the four pathogens in the ChEMBL records loaded here.
Docking
Computational · nothing measuredAutoDock 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 Voriconazole 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.
- Trimetrexate GlucuronateExisting use: Other agents against amoebiasis and other protozoal diseases88.6% AI-predicted activityagainst E. coliLab records exist17 registered studies
- Folic AcidExisting use: Acne, Anemia, Anemia (phenotype) and 8 more87.0% AI-predicted activityagainst E. coliLab records exist50+ registered studies
- MethotrexateExisting use: Acute lymphoblastic leukemia, Adenoma, Arthritis and 21 more86.8% AI-predicted activityagainst E. coliLab records exist50+ registered studies
- PralatrexateExisting use: Cancer, Mature T-cell and NK-cell non-Hodgkin lymphoma, Neoplasm and 2 more82.2% AI-predicted activityagainst E. coli44 registered studies
- TriclosanExisting use: Phenol and derivatives, Medicated dressings with antiinfectives81.0% AI-predicted activityagainst E. coliLab records exist50+ registered studies
- Leucovorin CalciumExisting use: Osteosarcoma67.6% AI-predicted activityagainst E. coli50+ registered studies
- LevoleucovorinExisting use: Anemia, Colorectal adenocarcinoma, Colorectal cancer and 3 more67.6% AI-predicted activityagainst E. coli50+ registered studies
- PyrimethamineExisting use: Malaria, Toxoplasmosis64.6% AI-predicted activityagainst E. coliLab records exist50+ registered studies
- Copanlisib DihydrochlorideExisting use: Follicular lymphoma, Neoplasm, Neoplasm of mature B-cells63.5% AI-predicted activityagainst E. coli10 registered studies
- AfamelanotideExisting use: Erythropoietic protoporphyria62.6% AI-predicted activityagainst E. coli23 registered studies
- Rimegepant SulfateExisting use: Migraine disorder61.6% AI-predicted activityagainst E. coli50+ registered studies
- Histrelin AcetateExisting use: Neoplasm, Prostate adenocarcinoma, Prostate cancer61.6% AI-predicted activityagainst E. coli13 registered studies
Registered studies
A registration describes a study; it does not establish a positive result.
Mycotic Ulcer Treatment Trial I
NCT00996736 · start 2010-04
Registered record
- Registry ID
- NCT00996736
- Conditions
- Corneal Ulcer; Eye Infections, Fungal
- Interventions
- Natamycin; Voriconazole
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2010-04
- Completion
- 2012-07
- Enrolment
- 323
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCorneal Ulcer; Eye Infections, FungalInterventionNatamycin; VoriconazolePhasePhase 3Registry statusCompletedDrug Interactions Between Voriconazole and Atazanavir Coadministered as Atazanavir/Ritonavir in Healthy Participants
NCT00833482 · start 2009-09
Registered record
- Registry ID
- NCT00833482
- Conditions
- Human Immunodeficiency Virus Type 1 (HIV-1); HIV Infections
- Interventions
- Voriconazole; Atazanavir; Ritonavir
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2009-09
- Completion
- 2011-02
- Enrolment
- 185
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHuman Immunodeficiency Virus Type 1 (HIV-1); HIV InfectionsInterventionVoriconazole; Atazanavir; RitonavirPhasePhase 1Registry statusCompletedA Pharmacokinetic And Safety Study Of Voriconazole In Healthy Male And Female Adults
NCT00855101 · start 2009-04
Registered record
- Registry ID
- NCT00855101
- Conditions
- Healthy Volunteers
- Interventions
- voriconazole
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2009-04
- Completion
- 2009-07
- Enrolment
- 35
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHealthy VolunteersInterventionvoriconazolePhasePhase 1Registry statusCompletedStudy Of The Pharmacokinetics And Safety Of Voriconazole In Children 2 To 11 Years Old Who Are At High Risk For Systemic Fungal Infection
NCT00739934 · start 2008-12
Registered record
- Registry ID
- NCT00739934
- Conditions
- Candidiasis; Candidemia
- Interventions
- voriconazole (Vfend)
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2008-12
- Completion
- 2009-10
- Enrolment
- 40
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCandidiasis; CandidemiaInterventionvoriconazole (Vfend)PhasePhase 2Registry statusCompletedVoriconazole Pharmacokinetics in Children With Gastrointestinal Graft Versus Host Disease
NCT00792246 · start 2008-12
Registered record
- Registry ID
- NCT00792246
- Conditions
- Graft Versus Host Disease; Stem Cell Transplantation
- Interventions
- voriconazole; voriconazole
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2008-12
- Completion
- 2012-07
- Enrolment
- 5
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionGraft Versus Host Disease; Stem Cell TransplantationInterventionvoriconazole; voriconazolePhasePhase 1Registry statusCompletedTMC125-TiDP2-C187: A Phase I, Open-label Trial to Investigate the Pharmacokinetic Interaction Between TMC125 and Two Antifungal Agents (Fluconazole and Voriconazole), All at Steady-state in Healthy Subjects.
NCT00740389 · start 2008-09
Registered record
- Registry ID
- NCT00740389
- Conditions
- HIV; AIDS; Fungal Infection
- Interventions
- TMC125
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2008-09
- Completion
- 2009-01
- Enrolment
- 18
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHIV; AIDS; Fungal InfectionInterventionTMC125PhasePhase 1Registry statusCompletedA Study To Assess The Anidulafungin And Voriconazole Concentration In Lung Following Intravenous Administration In Healthy Subjects
NCT00940017 · start 2008-09
Registered record
- Registry ID
- NCT00940017
- Conditions
- Aspergillosis; Candidemia
- Interventions
- anidulafungin and voriconazole
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2008-09
- Completion
- 2008-10
- Enrolment
- 24
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAspergillosis; CandidemiaInterventionanidulafungin and voriconazolePhasePhase 4Registry statusCompletedAnidulafungin Candidemia/Invasive Candidiasis Intensive Care Study
NCT00689338 · start 2008-07
Registered record
- Registry ID
- NCT00689338
- Conditions
- Invasive Candidiasis
- Interventions
- Anidulafungin; Fluconazole; Voriconazole
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2008-07
- Completion
- 2010-05
- Enrolment
- 216
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionInvasive CandidiasisInterventionAnidulafungin; Fluconazole; VoriconazolePhasePhase 3Registry statusCompletedA Multiple-Dose Study To Evaluate The Pharmacokinetics And Safety Of Voriconazole In Immunocompromised Adolescents
NCT00556998 · start 2008-06
Registered record
- Registry ID
- NCT00556998
- Conditions
- Pharmacokinetics
- Interventions
- Voriconazole
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2008-06
- Completion
- 2009-12
- Enrolment
- 26
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPharmacokineticsInterventionVoriconazolePhasePhase 2Registry statusCompletedAntifungal Prophylaxis in Pediatric Acute Leukemia
NCT00624143 · start 2008-02
Registered record
- Registry ID
- NCT00624143
- Conditions
- Pediatric Acute Leukemia Induction
- Interventions
- ORAL VORICONAZOLE and IV Amphotericin B
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Unknown
- Start
- 2008-02
- Completion
- Not recorded
- Enrolment
- 100
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPediatric Acute Leukemia InductionInterventionORAL VORICONAZOLE and IV Amphotericin BPhasePhase 3Registry statusUnknownAn Observational Analysis of Voriconazole Therapeutic Drug Concentration Monitoring, Pharmacogenomics and Clinical Outcome Correlations in High-risk Hematology Patients
NCT01321372 · start 2007-06
Registered record
- Registry ID
- NCT01321372
- Conditions
- Acute Leukemia
- Interventions
- Not recorded
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2007-06
- Completion
- 2011-06
- Enrolment
- 82
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAcute LeukemiaInterventionNot recordedPhaseNot recordedRegistry statusCompletedOpen, Non Comparative Study Of Voriconazole In Slovak Patients With Very High Risk Of Developing An Invasive Fungal Infection
NCT01137292 · start 2007-04
Registered record
- Registry ID
- NCT01137292
- Conditions
- Invasive Fungal Infections
- Interventions
- voriconazole (VFEND®)
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2007-04
- Completion
- 2009-11
- Enrolment
- 177
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionInvasive Fungal InfectionsInterventionvoriconazole (VFEND®)PhaseNot recordedRegistry statusCompletedBioavailability and Metabolism of Voriconazole in Relation to Its Modulation by the CYP2C19 Genetic Polymorphism
NCT00175994 · start 2005-07
Registered record
- Registry ID
- NCT00175994
- Conditions
- Healthy
- Interventions
- Not recorded
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2005-07
- Completion
- 2006-07
- Enrolment
- 24
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHealthyInterventionNot recordedPhaseNot recordedRegistry statusCompletedAn Open-Label Study To Assess The Pharmacokinetics, Safety And Toleration Of Vfend®; Following Multiple Dosing With Vfend
NCT00150319 · start 2005-06
Registered record
- Registry ID
- NCT00150319
- Conditions
- Kidney Failure
- Interventions
- Vfend®; I.V.
- Study type
- INTERVENTIONAL
- Phase
- Phase 1 / Phase 2
- Registry status
- Terminated
- Start
- 2005-06
- Completion
- 2005-10
- Enrolment
- 1
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionKidney FailureInterventionVfend®; I.V.PhasePhase 1 / Phase 2Registry statusTerminatedVoriconazole Prophylaxis Against Aspergillosis in Lung Transplant Recipients
NCT00177827 · start 2004-03
Registered record
- Registry ID
- NCT00177827
- Conditions
- Post Lung Transplantation
- Interventions
- Not recorded
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2004-03
- Completion
- 2006-03
- Enrolment
- 104
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPost Lung TransplantationInterventionNot recordedPhaseNot recordedRegistry statusCompleted