Carvedilol
FDA-approved product (tablet, oral), marketed as Carvedilol, Coreg, Carvedilol Phosphate and 1 more.
- Registered studies
- 50+
- Lab records
- 0
- Pathogens at ≥40%
- 1 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Cardiovascular disease
- Congestive heart failure
- Heart failure
- Hypertension
- Myocardial infarction
- Ventricular Dysfunction, Left
Indications ChEMBL records as approved, from FDA and DailyMed labels. Label ↗
- WHO therapeutic group
- Alpha and beta blocking agents
- FDA pharmacologic class
- alpha-Adrenergic Blocker; beta-Adrenergic Blocker 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 M. tuberculosis. It was surfaced computationally for further investigation; it is not an established treatment for this infection.
AI-predicted activity
AI prediction · nothing measured- MRSA25.9% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- E. coli28.4% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- K. pneumoniae16.6% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- M. tuberculosis55.4% 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 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 Carvedilol 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.
- Mefloquine HydrochlorideExisting use: Malaria, Plasmodium falciparum malaria, Plasmodium vivax malaria81.8% AI-predicted activityagainst M. tuberculosisLab records exist8 registered studies
- KetoconazoleExisting use: Adrenal gland disease, Blastomycosis, Cushing syndrome and 3 more81.2% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
- LevoketoconazoleExisting use: Adrenal gland disease, Adrenal gland hyperfunction, Cushing syndrome81.2% AI-predicted activityagainst M. tuberculosis6 registered studies
- Fluphenazine DecanoateExisting use: Mental or behavioural disorder, Psychosis80.7% AI-predicted activityagainst M. tuberculosis4 registered studies
- Fluphenazine EnanthateExisting use: Mental or behavioural disorder, Psychosis80.7% AI-predicted activityagainst M. tuberculosisNo documented evidence found
- NifurtimoxExisting use: American trypanosomiasis, Chagas disease, Leishmaniasis and 1 more78.4% AI-predicted activityagainst M. tuberculosis19 registered studies
- Fluphenazine HydrochlorideExisting use: Mental or behavioural disorder, Psychosis77.8% AI-predicted activityagainst M. tuberculosis5 registered studies
- NitazoxanideExisting use: Amebiasis, Diarrhea77.8% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
- TopiramateExisting use: Epilepsy, Lennox-Gastaut syndrome, Migraine disorder and 1 more77.4% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
- TrabectedinExisting use: Cancer, Dedifferentiated liposarcoma, Leiomyosarcoma and 7 more76.8% AI-predicted activityagainst M. tuberculosis50+ registered studies
- Chlorpromazine HydrochlorideExisting use: Conduct disorder, Mental or behavioural disorder, Nausea and vomiting and 3 more75.0% AI-predicted activityagainst M. tuberculosis33 registered studies
- ProchlorperazineExisting use: Anxiety disorder, Nausea and vomiting, Psychosis and 1 more74.1% AI-predicted activityagainst M. tuberculosis50+ registered studies
Registered studies
A registration describes a study; it does not establish a positive result.
Impact of Bariatric Surgery on Pharmacokinetic Study of Simvastatin and Carvedilol
NCT04049786 · start 2019-06-01
Registered record
- Registry ID
- NCT04049786
- Conditions
- Obesity; Bariatric Surgery; Roux-en Y Gastric Bypass
- Interventions
- Digestive biopsy; Carvedilol 25mg; Serial blood sampling for PK analysis; Metoprolol 100 mg for CYP2D6 phenotyping; Simvastatin 40mg; Midazolam 2 mg for CYP3A4 phenotyping; Genotyping
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Unknown
- Start
- 2019-06-01
- Completion
- 2023-08
- Enrolment
- 120
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionObesity; Bariatric Surgery; Roux-en Y Gastric BypassInterventionDigestive biopsy; Carvedilol 25mg; Serial blood sampling for PK analysis; Metoprolol 100 mg for CYP2D6 phenotyping +3 morePhasePhase 4Registry statusUnknownEffects of Sleep Deprivation and Adrenergic Inhibition on Glymphatic Flow in Humans
NCT03576664 · start 2018-08-28
Registered record
- Registry ID
- NCT03576664
- Conditions
- Sleep Deprivation; Sleep Wake Disorders; Sleep
- Interventions
- Carvedilol 25mg; Placebo oral capsule
- Study type
- INTERVENTIONAL
- Phase
- Early phase 1
- Registry status
- Completed
- Start
- 2018-08-28
- Completion
- 2019-10-01
- Enrolment
- 22
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSleep Deprivation; Sleep Wake Disorders; SleepInterventionCarvedilol 25mg; Placebo oral capsulePhaseEarly phase 1Registry statusCompletedDetecting and Treating Subclinical Anthracycline Therapy Related Cardiac Dysfunction in Low Income Country.
NCT03542058 · start 2018-06
Registered record
- Registry ID
- NCT03542058
- Conditions
- Chemotherapy Related Cardiac Dysfunction
- Interventions
- Carvedilol
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Unknown
- Start
- 2018-06
- Completion
- 2021-06
- Enrolment
- 50
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionChemotherapy Related Cardiac DysfunctionInterventionCarvedilolPhasePhase 3Registry statusUnknownCarvedilol for Prevention of Esophageal Varices Progression
NCT03736265 · start 2017-10-09
Registered record
- Registry ID
- NCT03736265
- Conditions
- Cirrhosis, Liver; Portal Hypertension
- Interventions
- Carvedilol
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Unknown
- Start
- 2017-10-09
- Completion
- 2022-12-30
- Enrolment
- 240
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCirrhosis, Liver; Portal HypertensionInterventionCarvedilolPhaseNot applicableRegistry statusUnknownRate Control in Atrial Fibrillation
NCT02251509 · start 2016-12
Registered record
- Registry ID
- NCT02251509
- Conditions
- Atrial Fibrillation
- Interventions
- Carvedilol; Metoprolol tartrate
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Unknown
- Start
- 2016-12
- Completion
- 2017-09
- Enrolment
- 20
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAtrial FibrillationInterventionCarvedilol; Metoprolol tartratePhasePhase 4Registry statusUnknownLeft Cardiac Sympathetic Denervation for Cardiomyopathy Feasibility Pilot Study
NCT03071653 · start 2016-11-24
Registered record
- Registry ID
- NCT03071653
- Conditions
- Dilated Cardiomyopathy; Ischemic Cardiomyopathy; Non-ischemic Cardiomyopathy
- Interventions
- Left Cardiac Sympathetic Denervation (LCSD); Optimal Medical Therapy
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Suspended
- Start
- 2016-11-24
- Completion
- 2022-02
- Enrolment
- 30
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionDilated Cardiomyopathy; Ischemic Cardiomyopathy; Non-ischemic CardiomyopathyInterventionLeft Cardiac Sympathetic Denervation (LCSD); Optimal Medical TherapyPhasePhase 2Registry statusSuspendedBeta-blockers in Pulmonary Arterial Hypertension
NCT02507011 · start 2016-01-31
Registered record
- Registry ID
- NCT02507011
- Conditions
- Pulmonary Arterial Hypertension
- Interventions
- Carvedilol; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Terminated
- Start
- 2016-01-31
- Completion
- 2019-07-01
- Enrolment
- 2
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPulmonary Arterial HypertensionInterventionCarvedilol; PlaceboPhasePhase 2Registry statusTerminatedThe Effect of Carvedilol VS Endoscopic Therapy in Primary Prophylaxis of High-risk Esophageal Gastric Variceal Bleeding
NCT02695732 · start 2015-12
Registered record
- Registry ID
- NCT02695732
- Conditions
- Liver Cirrhosis; Esophageal and Gastric Varices
- Interventions
- Carvedilol; endoscopy
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Unknown
- Start
- 2015-12
- Completion
- 2018-09
- Enrolment
- 792
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionLiver Cirrhosis; Esophageal and Gastric VaricesInterventionCarvedilol; endoscopyPhasePhase 4Registry statusUnknownRemoval of Beta Blocker Drugs by Hemodialysis
NCT03361280 · start 2015-02-27
Registered record
- Registry ID
- NCT03361280
- Conditions
- Chronic Kidney Diseases
- Interventions
- Beta blocker
- Study type
- INTERVENTIONAL
- Phase
- Phase 1 / Phase 2
- Registry status
- Completed
- Start
- 2015-02-27
- Completion
- 2016-03-10
- Enrolment
- 8
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionChronic Kidney DiseasesInterventionBeta blockerPhasePhase 1 / Phase 2Registry statusCompletedMechanisms of Refractory Hypertension (Carvedilol)
NCT02357004 · start 2015-02
Registered record
- Registry ID
- NCT02357004
- Conditions
- Hypertensive
- Interventions
- Carvedilol; Chlorthalidone
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Withdrawn
- Start
- 2015-02
- Completion
- 2020-01-31
- Enrolment
- 0
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHypertensiveInterventionCarvedilol; ChlorthalidonePhaseNot applicableRegistry statusWithdrawnEarly Precise Diagnosis and Intervention of CPT Based on a Noninvasive 3D-vHPS
NCT02925975 · start 2015-01
Registered record
- Registry ID
- NCT02925975
- Conditions
- Portal Hypertension; Cirrhosis
- Interventions
- Carvedilol; 3D-vHPS; Routine endoscopic procedures
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Unknown
- Start
- 2015-01
- Completion
- 2020-06
- Enrolment
- 100
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPortal Hypertension; CirrhosisInterventionCarvedilol; 3D-vHPS; Routine endoscopic proceduresPhasePhase 4Registry statusUnknownDoppler Ultrasound Hepatic Vein Waveform as a Non-invasive Tool in the Assessment of Severity of Portal Hypertension
NCT02975323 · start 2014-12
Registered record
- Registry ID
- NCT02975323
- Conditions
- Portal Hypertension
- Interventions
- Carvedilol
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Unknown
- Start
- 2014-12
- Completion
- 2018-12
- Enrolment
- 50
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPortal HypertensionInterventionCarvedilolPhasePhase 3Registry statusUnknownSystematic Withdrawal of Neurohumoral Blocker Therapy in Optimally Responding CRT Patients
NCT02200822 · start 2014-07
Registered record
- Registry ID
- NCT02200822
- Conditions
- Heart Failure (HF)
- Interventions
- beta blockers; RAAS blockers
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2014-07
- Completion
- 2019-02
- Enrolment
- 80
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHeart Failure (HF)Interventionbeta blockers; RAAS blockersPhasePhase 4Registry statusCompletedA Study in Healthy Volunteers to Evaluate the Application of Stable Isotope Approach to Reduce Number of Subjects Needed for PK Studies
NCT01793870 · start 2013-01-15
Registered record
- Registry ID
- NCT01793870
- Conditions
- Metabolic, Cardiovascular
- Interventions
- Tab carvedilol 25 mg; Tab carvedilol 6.25 mg; Powder carvedilol up to 2.5 mg
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2013-01-15
- Completion
- 2013-06-17
- Enrolment
- 17
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMetabolic, CardiovascularInterventionTab carvedilol 25 mg; Tab carvedilol 6.25 mg; Powder carvedilol up to 2.5 mgPhasePhase 1Registry statusCompletedRemission From Stage D Heart Failure
NCT01774656 · start 2013-01
Registered record
- Registry ID
- NCT01774656
- Conditions
- Heart Failure NYHA Class III; Heart Failure NYHA Class IV
- Interventions
- Pharmacological Treatment
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Unknown
- Start
- 2013-01
- Completion
- 2017-12
- Enrolment
- 40
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHeart Failure NYHA Class III; Heart Failure NYHA Class IVInterventionPharmacological TreatmentPhasePhase 4Registry statusUnknown