Pravastatin Sodium
FDA-approved product (tablet, oral), marketed as Pravachol, Pravastatin Sodium.
- Registered studies
- 50+
- Lab records
- 0
- Pathogens at ≥40%
- 2 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Atherosclerosis
- Cardiovascular disease
- Coronary artery disease
- Coronary atherosclerosis
- Familial hypercholesterolemia
- Hypercholesterolemia
- Myocardial infarction
Indications ChEMBL records as approved, from FDA and DailyMed labels. Label ↗
- WHO therapeutic group
- Hmg coa reductase inhibitors
- Anti-infective classification
- Not classified as an anti-infective.
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- MRSA46.5% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- E. coli34.6% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- K. pneumoniae28.3% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- M. tuberculosis47.3% 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 Pravastatin Sodium 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.
- Pafolacianine SodiumExisting use: Other diagnostic agents61.4% AI-predicted activityagainst E. coli1 registered study
- LinaclotideExisting use: Constipation, Constipation disorder, Irritable bowel syndrome60.5% AI-predicted activityagainst E. coli50+ registered studies
- PlecanatideExisting use: Constipation60.1% AI-predicted activityagainst E. coli15 registered studies
- Terazosin HydrochlorideExisting use: Benign prostatic hyperplasia60.0% AI-predicted activityagainst E. coli41 registered studies
- Leuprolide AcetateExisting use: Central precocious puberty, Metastatic prostate cancer, Neoplasm and 4 more59.6% AI-predicted activityagainst E. coli50+ registered studies
- Trilaciclib DihydrochlorideExisting use: Small cell lung carcinoma59.6% AI-predicted activityagainst E. coli2 registered studies
- Gonadorelin AcetateExisting use: Gonadotropin-releasing hormones, Tests for fertility disturbances59.5% AI-predicted activityagainst E. coli50+ registered studies
- Larotrectinib SulfateExisting use: Abdominal Neoplasms, Cancer, Metastasis and 1 more59.4% AI-predicted activityagainst E. coli5 registered studies
- PalbociclibExisting use: Breast cancer, Breast carcinoma, Breast neoplasm and 3 more59.1% AI-predicted activityagainst E. coli50+ registered studies
- TemsirolimusExisting use: Cancer, Clear cell renal carcinoma, Mantle cell lymphoma and 2 more59.0% AI-predicted activityagainst E. coli50+ registered studies
- Angiotensin Ii AcetateExisting use: Cardiovascular disease, Hypotension, Septic shock and 1 more58.8% AI-predicted activityagainst E. coli10 registered studies
- Terlipressin AcetateExisting use: Hepatorenal syndrome, Kidney failure, Renal insufficiency58.8% AI-predicted activityagainst E. coli7 registered studies
Registered studies
A registration describes a study; it does not establish a positive result.
Quality of Life in Patients With Statin-Associated Myopathy
NCT00850460 · start 2009-02
Registered record
- Registry ID
- NCT00850460
- Conditions
- Statin Adverse Reaction
- Interventions
- Statins; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Terminated
- Start
- 2009-02
- Completion
- 2013-02
- Enrolment
- 14
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionStatin Adverse ReactionInterventionStatins; PlaceboPhasePhase 4Registry statusTerminatedEfficacy and Safety of Prescription Omega-3 Fatty Acid Added to Stable Statin Therapy in Patients With Type 2 Diabetes and Hypertriglyceridemia
NCT02305355 · start 2009-02
Registered record
- Registry ID
- NCT02305355
- Conditions
- Diabetes Mellitus, Type 2; Hypertriglycemia
- Interventions
- Omega-3-acids ethylesters 90 4g; Pravastatin, Simvastatin, Atorvastatin, Rosuvastatin
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2009-02
- Completion
- 2011-02
- Enrolment
- 68
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionDiabetes Mellitus, Type 2; HypertriglycemiaInterventionOmega-3-acids ethylesters 90 4g; Pravastatin, Simvastatin, Atorvastatin, RosuvastatinPhasePhase 4Registry statusCompletedSouth Korean Pitavastatin Heart Failure Study
NCT00701285 · start 2008-07
Registered record
- Registry ID
- NCT00701285
- Conditions
- Chronic Heart Failure
- Interventions
- pitavastatin; pravastatin
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2008-07
- Completion
- 2014-05
- Enrolment
- 70
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionChronic Heart FailureInterventionpitavastatin; pravastatinPhasePhase 4Registry statusCompletedGenetic Predictors of Variability in the Drug-drug Interaction Between Darunavir/Ritonavir and Pravastatin
NCT00630734 · start 2008-02
Registered record
- Registry ID
- NCT00630734
- Conditions
- HIV Infections; Hyperlipidemia
- Interventions
- Pravastatin; Darunavir; Ritonavir; Pravastatin; Washout
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2008-02
- Completion
- 2010-09
- Enrolment
- 32
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHIV Infections; HyperlipidemiaInterventionPravastatin; Darunavir; Ritonavir; Pravastatin +1 morePhasePhase 4Registry statusCompletedObservational Study of Approaches to Lipid-Lowering Therapy in Russian Patients With Coronary Heart Disease <<Treat to Goal>> (Study P05464)
NCT00730132 · start 2008-01
Registered record
- Registry ID
- NCT00730132
- Conditions
- Coronary Heart Disease; Hypercholesterolemia
- Interventions
- Ezetimibe; Statin
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2008-01
- Completion
- 2009-08
- Enrolment
- 712
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCoronary Heart Disease; HypercholesterolemiaInterventionEzetimibe; StatinPhaseNot recordedRegistry statusCompletedA Study to Evaluate Daily Pravastatin, Fenofibrate or Pravafen in the Treatment of Combined Hyperlipidemia
NCT00459745 · start 2007-04
Registered record
- Registry ID
- NCT00459745
- Conditions
- Combined Hyperlipidemia
- Interventions
- Pravafen; Pravastatin; Fenofibrate
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2007-04
- Completion
- 2009-07
- Enrolment
- 481
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCombined HyperlipidemiaInterventionPravafen; Pravastatin; FenofibratePhasePhase 3Registry statusCompletedPilot Study of a Multi-Drug Regimen for Severe Pulmonary Fibrosis in Hermansky-Pudlak Syndrome
NCT00467831 · start 2007-04
Registered record
- Registry ID
- NCT00467831
- Conditions
- Hermansky-Pudlak Syndrome (HPS); Pulmonary Fibrosis; Oculocutaneous Albinism; Platelet Storage Pool Deficiency; Metabolic Disease
- Interventions
- Losartan; Zileuton; N-Acetylcysteine; Pravastatin; Erythromycin
- Study type
- INTERVENTIONAL
- Phase
- Phase 1 / Phase 2
- Registry status
- Terminated
- Start
- 2007-04
- Completion
- 2012-11
- Enrolment
- 3
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHermansky-Pudlak Syndrome (HPS); Pulmonary Fibrosis; Oculocutaneous Albinism; Platelet Storage Pool Deficiency +1 moreInterventionLosartan; Zileuton; N-Acetylcysteine; Pravastatin +1 morePhasePhase 1 / Phase 2Registry statusTerminatedEtoposide and Cisplatin or Carboplatin as First-Line Chemotherapy With or Without Pravastatin in Treating Patients With Small Cell Lung Cancer
NCT00433498 · start 2007-01
Registered record
- Registry ID
- NCT00433498
- Conditions
- Lung Cancer
- Interventions
- carboplatin; cisplatin; etoposide phosphate; pravastatin sodium
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2007-01
- Completion
- 2013-11
- Enrolment
- 846
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionLung CancerInterventioncarboplatin; cisplatin; etoposide phosphate; pravastatin sodiumPhasePhase 3Registry statusCompletedPravastatin 80 mg Tablets Dosed in Healthy Subjects Under Non-Fasting Conditions
NCT00829309 · start 2005-03
Registered record
- Registry ID
- NCT00829309
- Conditions
- Healthy
- Interventions
- Pravastatin; Pravastatin
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2005-03
- Completion
- 2005-03
- Enrolment
- 16
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHealthyInterventionPravastatin; PravastatinPhasePhase 1Registry statusCompletedJapan Statin Treatment Against Recurrent Stroke (J-STARS)
NCT00221104 · start 2004-03-01
Registered record
- Registry ID
- NCT00221104
- Conditions
- Ischemic Stroke
- Interventions
- Pravastatin
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2004-03-01
- Completion
- Not recorded
- Enrolment
- 1,578
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionIschemic StrokeInterventionPravastatinPhasePhase 3Registry statusCompletedImproving Symptoms of Schizophrenia and Schizoaffective Disorder by Supplementing Medications With Pravastatin
NCT00177580 · start 2003-07
Registered record
- Registry ID
- NCT00177580
- Conditions
- Schizophrenia; Schizoaffective Disorder
- Interventions
- Pravastatin
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2003-07
- Completion
- 2007-07
- Enrolment
- 72
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSchizophrenia; Schizoaffective DisorderInterventionPravastatinPhasePhase 4Registry statusCompletedFasting Bioequivalence Study of Pravastatin Sodium 80 mg Tablets Versus Pravachol® 80 mg Tablets In Normal Healthy Subjects
NCT00650221 · start 2003-06
Registered record
- Registry ID
- NCT00650221
- Conditions
- Therapeutic Equivalency
- Interventions
- Pravastatin; Pravastatin
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2003-06
- Completion
- 2003-07
- Enrolment
- 43
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionTherapeutic EquivalencyInterventionPravastatin; PravastatinPhasePhase 1Registry statusCompletedPrevention of Atherosclerosis and Heart Disease in Patients With Systemic Lupus Erythematosis (SLE)
NCT00054938 · start 2003-03
Registered record
- Registry ID
- NCT00054938
- Conditions
- Systemic Lupus Erythematosus; Lupus
- Interventions
- pravastatin; aspirin; ramipril; Vitamins: B6, B12, and folate; heart health educational program
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2003-03
- Completion
- 2005-12
- Enrolment
- 150
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSystemic Lupus Erythematosus; LupusInterventionpravastatin; aspirin; ramipril; Vitamins: B6, B12, and folate +1 morePhasePhase 2Registry statusCompletedPravastatin for Hyperlipidaemia in HIV.
NCT00227500 · start 2001-07
Registered record
- Registry ID
- NCT00227500
- Conditions
- HIV Infections; Lipid Metabolism; Glucose Metabolism; Metabolic Abnormality; Lipodystrophy; Cardiovascular Disease
- Interventions
- Pravastatin
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2001-07
- Completion
- 2004-10
- Enrolment
- 40
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHIV Infections; Lipid Metabolism; Glucose Metabolism; Metabolic Abnormality +2 moreInterventionPravastatinPhasePhase 4Registry statusCompletedBioavailability Study of Pravastatin Sodium 40 mg Tablets Under Fasting Conditions
NCT00834379 · start 2000-09
Registered record
- Registry ID
- NCT00834379
- Conditions
- Healthy
- Interventions
- pravastatin sodium; Pravachol®
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2000-09
- Completion
- 2000-09
- Enrolment
- 58
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHealthyInterventionpravastatin sodium; Pravachol®PhasePhase 1Registry statusCompleted