Trandolapril
FDA-approved product (tablet, oral), marketed as Mavik, Trandolapril.
- Registered studies
- 29
- Lab records
- 0
- Pathogens at ≥40%
- 1 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Cardiovascular disease
- Heart failure
- Hypertension
- Myocardial infarction
- Ventricular Dysfunction, Left
Indications ChEMBL records as approved, from FDA and DailyMed labels. Label ↗
- WHO therapeutic group
- Ace inhibitors, plain
- FDA pharmacologic class
- Angiotensin Converting Enzyme 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 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- MRSA37.1% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- E. coli26.1% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- K. pneumoniae18.2% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- M. tuberculosis61.9% 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
29registered studies name this medicine, for any condition. 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 Trandolapril 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.
- Galantamine HydrobromideExisting use: Alzheimer disease, Dementia89.6% AI-predicted activityagainst K. pneumoniaeLab records exist50+ registered studies
- Chlorhexidine GluconateExisting use: Eye infection, Gingivitis, Infection and 2 more69.3% AI-predicted activityagainst K. pneumoniaeLab records exist50+ registered studies
- TriclosanExisting use: Phenol and derivatives, Medicated dressings with antiinfectives68.0% AI-predicted activityagainst K. pneumoniaeLab records exist50+ registered studies
- ElvitegravirExisting use: HIV infection, HIV-1 infection, Viral disease60.2% AI-predicted activityagainst K. pneumoniae50+ registered studies
- Caspofungin AcetateExisting use: Aspergillosis, Candidemia, Candidiasis and 1 more57.5% AI-predicted activityagainst K. pneumoniae50+ registered studies
- DactinomycinExisting use: Kidney Wilms tumor, Neoplasm56.8% AI-predicted activityagainst K. pneumoniae50+ registered studies
- CyclosporineExisting use: Conjunctivitis, Corneal disease, Eye disease and 6 more56.1% AI-predicted activityagainst K. pneumoniae50+ registered studies
- LinaclotideExisting use: Constipation, Constipation disorder, Irritable bowel syndrome56.0% AI-predicted activityagainst K. pneumoniae50+ registered studies
- Irinotecan HydrochlorideExisting use: Adenocarcinoma, Cancer, Carcinoma and 4 more54.5% AI-predicted activityagainst K. pneumoniae50+ registered studies
- OxytocinExisting use: Hemorrhage, Uterine Inertia52.7% AI-predicted activityagainst K. pneumoniae50+ registered studies
- Micafungin SodiumExisting use: Candidiasis52.4% AI-predicted activityagainst K. pneumoniae50+ registered studies
- VoclosporinExisting use: Immune system disease, Lupus nephritis52.2% AI-predicted activityagainst K. pneumoniae28 registered studies
Registered studies
A registration describes a study; it does not establish a positive result.
Evaluation of Heart Failure Treatment Guided by N-terminal Pro B-type Natriuretic Peptide (NTproBNP) vs Clinical Symptoms and Signs Alone
NCT00391846 · start 2006-10
Registered record
- Registry ID
- NCT00391846
- Conditions
- Heart Failure; Ventricular Dysfunction, Left
- Interventions
- Captopril; Enalapril; Lisinopril; Ramipril; Trandolapril; Bisoprolol; Carvedilol; Metoprolol succinate; Candesartan; Valsartan; Eplerenone; Spironolactone; Diuretics; HF treatment according to Swedish guidelines; Blood samples; The Kansas City Cardiomyopathy Questionnaire (KCCQ)
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2006-10
- Completion
- 2009-01
- Enrolment
- 252
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHeart Failure; Ventricular Dysfunction, LeftInterventionCaptopril; Enalapril; Lisinopril; Ramipril +12 morePhasePhase 4Registry statusCompletedBioequivalence Study of Trandolapril 4 mg Tablets of Dr. Reddy's Under Fasting Conditions
NCT01164787 · start 2006-03
Registered record
- Registry ID
- NCT01164787
- Conditions
- Healthy
- Interventions
- Trandolapril; Mavik
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2006-03
- Completion
- 2006-05
- Enrolment
- 52
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHealthyInterventionTrandolapril; MavikPhasePhase 1Registry statusCompletedBioequivalence Study of Trandolapril 4 mg Tablets of Dr. Reddy's Under Fed Conditions
NCT01164800 · start 2006-03
Registered record
- Registry ID
- NCT01164800
- Conditions
- Healthy
- Interventions
- Trandolapril; Mavik
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2006-03
- Completion
- 2006-05
- Enrolment
- 52
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHealthyInterventionTrandolapril; MavikPhasePhase 1Registry statusCompletedAcute Haemodynamic Effects of Treatment With Angiotensin Converting Enzyme (ACE)-Inhibitors in Patients With Symptomatic Aortic Stenosis
NCT00252317 · start 2005-11
Registered record
- Registry ID
- NCT00252317
- Conditions
- Aortic Stenosis
- Interventions
- Captopril and Trandolapril; Captopril Test Dose and Trandolapril
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Unknown
- Start
- 2005-11
- Completion
- 2008-10
- Enrolment
- 64
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAortic StenosisInterventionCaptopril and Trandolapril; Captopril Test Dose and TrandolaprilPhasePhase 4Registry statusUnknownTrandolapril 4 mg Tablet Under Non-Fasting Conditions
NCT00840073 · start 2004-10
Registered record
- Registry ID
- NCT00840073
- Conditions
- Healthy
- Interventions
- Trandolapril 4 mg Tablets; Mavik® 4 mg Tablets
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2004-10
- Completion
- 2004-11
- Enrolment
- 50
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHealthyInterventionTrandolapril 4 mg Tablets; Mavik® 4 mg TabletsPhasePhase 1Registry statusCompletedTrandolapril 4 mg Tablet Under Fasting Conditions
NCT00840632 · start 2004-10
Registered record
- Registry ID
- NCT00840632
- Conditions
- Healthy
- Interventions
- Trandolapril 4 mg Tablets; Mavik® 4 mg Tablets
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2004-10
- Completion
- 2004-11
- Enrolment
- 40
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHealthyInterventionTrandolapril 4 mg Tablets; Mavik® 4 mg TabletsPhasePhase 1Registry statusCompletedRussian Study of the Efficacy and Safety of Tarka in Patients With Hypertension
NCT00235001 · start 2004-06
Registered record
- Registry ID
- NCT00235001
- Conditions
- Hypertension
- Interventions
- trandolapril/verapamil
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2004-06
- Completion
- Not recorded
- Enrolment
- 120
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHypertensionInterventiontrandolapril/verapamilPhasePhase 4Registry statusCompletedCanadian Study of Trandolapril on Blood Pressure in Hypertensive Patients (TRAIL)
NCT00233532 · start 2004-03
Registered record
- Registry ID
- NCT00233532
- Conditions
- Hypertension
- Interventions
- Trandolapril
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2004-03
- Completion
- Not recorded
- Enrolment
- 2,000
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHypertensionInterventionTrandolaprilPhasePhase 4Registry statusCompletedTarka vs. Hyzaar in Patients With Metabolic Syndrome (STAR)
NCT00234858 · start 2004-03
Registered record
- Registry ID
- NCT00234858
- Conditions
- Hypertension; Metabolic Syndrome
- Interventions
- trandolapril/verapamil; (Hyzaar) losartan/hydrochlorothiazide
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2004-03
- Completion
- Not recorded
- Enrolment
- 280
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHypertension; Metabolic SyndromeInterventiontrandolapril/verapamil; (Hyzaar) losartan/hydrochlorothiazidePhasePhase 4Registry statusCompletedTarka® vs. Lotrel® in Hypertensive, Diabetic Subjects With Renal Disease (TANDEM)
NCT00234871 · start 2004-01
Registered record
- Registry ID
- NCT00234871
- Conditions
- Hypertension; Diabetes; Proteinuria
- Interventions
- trandolapril/verapamil; Lotrel (amlodipine/benazepril)
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2004-01
- Completion
- Not recorded
- Enrolment
- 357
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHypertension; Diabetes; ProteinuriaInterventiontrandolapril/verapamil; Lotrel (amlodipine/benazepril)PhasePhase 4Registry statusCompletedRenin-Guided Therapeutics in the Management of Untreated, Uncontrolled, or Complicated Hypertension
NCT00684489 · start 2003-09
Registered record
- Registry ID
- NCT00684489
- Conditions
- Hypertension
- Interventions
- clinical hypertension specialist-no specific med. Any anti-hypertension meds.; renin guided therapeutics-no specific med. Any anti-hypertensive med.
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2003-09
- Completion
- 2005-09
- Enrolment
- 52
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHypertensionInterventionclinical hypertension specialist-no specific med. Any anti-hypertension meds.; renin guided therapeutics-no specific med. Any anti-hypertensive med.PhaseNot applicableRegistry statusCompletedBlood Pressure and Weight Trajectory on a Dual Antihypertensive Combination Plus Sibutramine Versus Placebo in Obese Hypertensives
NCT00679653 · start 2002-02
Registered record
- Registry ID
- NCT00679653
- Conditions
- Obesity; Hypertension
- Interventions
- sibutramine; sibutramine; verapamil/trandolapril; metoprolol/HCT; felodipine/ramipril
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2002-02
- Completion
- Not recorded
- Enrolment
- 171
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionObesity; HypertensionInterventionsibutramine; sibutramine; verapamil/trandolapril; metoprolol/HCT +1 morePhasePhase 3Registry statusCompletedINVEST: INternational VErapamil SR Trandolapril STudy
NCT00133692 · start 1997-09
Registered record
- Registry ID
- NCT00133692
- Conditions
- Hypertension; Coronary Artery Disease
- Interventions
- Verapamil SR/Trandolapril/Hydrochlorothiazide (HCTZ); Atenolol/HCTZ/Trandolapril
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 1997-09
- Completion
- 2003-02
- Enrolment
- 22,000
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHypertension; Coronary Artery DiseaseInterventionVerapamil SR/Trandolapril/Hydrochlorothiazide (HCTZ); Atenolol/HCTZ/TrandolaprilPhasePhase 4Registry statusCompletedA Study for Prevention of Kidney Disease in Diabetic Patients (BENEDICT)
NCT00235014 · start 1997-03
Registered record
- Registry ID
- NCT00235014
- Conditions
- Hypertension; Diabetes
- Interventions
- trandolapril; trandolapril/verapamil; placebo; verapamil
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 1997-03
- Completion
- Not recorded
- Enrolment
- 1,204
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHypertension; DiabetesInterventiontrandolapril; trandolapril/verapamil; placebo; verapamilPhasePhase 4Registry statusCompleted