Ezetimibe
FDA-approved product (tablet, oral), marketed as Ezetimibe, Zetia.
- Registered studies
- 50+
- Lab records
- 0
- Pathogens at ≥40%
- 3 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Cardiovascular disease
- Familial hypercholesterolemia
- Homozygous familial hypercholesterolemia
- Hypercholesterolemia
- Hyperlipidemia
Indications ChEMBL records as approved, from FDA and DailyMed labels. Label ↗
- WHO therapeutic group
- Other lipid modifying agents
- FDA pharmacologic class
- Dietary Cholesterol Absorption Inhibitor FDA label ↗
- Anti-infective classification
- Not classified as an anti-infective.
Repurposing investigation
This medicine is being investigated here for AI-predicted antimicrobial activity against MRSA, E. coli 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- MRSA48.0% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- E. coli43.1% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- K. pneumoniae36.5% 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 Ezetimibe 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.
- Etrasimod ArginineExisting use: Ulcerative colitis64.1% AI-predicted activityagainst MRSANo documented evidence found
- MethotrexateExisting use: Acute lymphoblastic leukemia, Adenoma, Arthritis and 21 more64.1% AI-predicted activityagainst MRSA50+ registered studies
- KetoconazoleExisting use: Adrenal gland disease, Blastomycosis, Cushing syndrome and 3 more63.6% AI-predicted activityagainst MRSA50+ registered studies
- LevoketoconazoleExisting use: Adrenal gland disease, Adrenal gland hyperfunction, Cushing syndrome63.6% AI-predicted activityagainst MRSA6 registered studies
- Nafarelin AcetateExisting use: Endometriosis63.6% AI-predicted activityagainst MRSA12 registered studies
- Pafolacianine SodiumExisting use: Other diagnostic agents63.6% AI-predicted activityagainst MRSA1 registered study
- Vinorelbine TartrateExisting use: Cancer, Neoplasm63.6% AI-predicted activityagainst MRSA50+ registered studies
- Ibrexafungerp CitrateExisting use: Vulvovaginal candidiasis63.5% AI-predicted activityagainst MRSANo documented evidence found
- Gonadorelin AcetateExisting use: Gonadotropin-releasing hormones, Tests for fertility disturbances63.4% AI-predicted activityagainst MRSA50+ registered studies
- Icatibant AcetateExisting use: Angioedema, Hereditary angioedema63.4% AI-predicted activityagainst MRSA33 registered studies
- LonafarnibExisting use: Hutchinson-Gilford progeria syndrome, Laminopathies, Progeria63.3% AI-predicted activityagainst MRSA39 registered studies
- LypressinExisting use: Vasopressin and analogues63.2% AI-predicted activityagainst MRSA50+ registered studies
Registered studies
A registration describes a study; it does not establish a positive result.
A Multicenter Study to Evaluate the Cholesterol Lowering Effects of Two Marketed Products in Patients With Type 2 Diabetes Mellitus and Hypercholesterolemia (MK-0653A-077)
NCT00110435 · start 2005-05
Registered record
- Registry ID
- NCT00110435
- Conditions
- Type 2 Diabetes Mellitus; Hypercholesterolemia
- Interventions
- MK0653A, ezetimibe (+) simvastatin; Duration of Treatment: 4 wk placebo run in then 6 wk active; Comparator: atorvastatin
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2005-05
- Completion
- 2005-12
- Enrolment
- 1,229
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionType 2 Diabetes Mellitus; HypercholesterolemiaInterventionMK0653A, ezetimibe (+) simvastatin; Duration of Treatment: 4 wk placebo run in then 6 wk active; Comparator: atorvastatinPhasePhase 3Registry statusCompletedEffects on NF-κB Activity: High Dose Simvastatin Versus Combination Therapy With Ezetimibe
NCT01424891 · start 2004-04
Registered record
- Registry ID
- NCT01424891
- Conditions
- Type 2 Diabetes; Inflammation
- Interventions
- Simvastatin 80 mg; Sim10/Eze10; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2004-04
- Completion
- 2011-08
- Enrolment
- 31
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionType 2 Diabetes; InflammationInterventionSimvastatin 80 mg; Sim10/Eze10; PlaceboPhaseNot applicableRegistry statusCompletedStudy of an Approved Drug With a Statin (a Medication That Lowers Cholesterol Levels) as Compared to Statin Therapy Alone in Patients With High Cholesterol (0653-040)
NCT00092586 · start 2002-09
Registered record
- Registry ID
- NCT00092586
- Conditions
- Hypercholesterolemia
- Interventions
- MK0653, ezetimibe; Comparator: statins
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2002-09
- Completion
- 2003-10
- Enrolment
- 2,904
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHypercholesterolemiaInterventionMK0653, ezetimibe; Comparator: statinsPhasePhase 3Registry statusCompletedInvestigational Drug in Patients With Hypercholesterolemia or in Patients With Sitosterolemia (0653-026)(COMPLETED)
NCT00092833 · start 2002-07
Registered record
- Registry ID
- NCT00092833
- Conditions
- Hypercholesterolemia, Familial; Lipid Metabolism, Inborn Errors
- Interventions
- Comparator: ezetimibe
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Terminated
- Start
- 2002-07
- Completion
- 2005-05
- Enrolment
- 49
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHypercholesterolemia, Familial; Lipid Metabolism, Inborn ErrorsInterventionComparator: ezetimibePhasePhase 3Registry statusTerminatedSitosterolemia Extension Study (0653-004)(COMPLETED)
NCT00092820 · start 2001-02-12
Registered record
- Registry ID
- NCT00092820
- Conditions
- Lipid Metabolism, Inborn Errors; Heart Disease
- Interventions
- MK0653, ezetimibe; Comparator: placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2001-02-12
- Completion
- 2004-11-30
- Enrolment
- 58
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionLipid Metabolism, Inborn Errors; Heart DiseaseInterventionMK0653, ezetimibe; Comparator: placeboPhasePhase 3Registry statusCompleted