Pitavastatin Sodium
FDA-approved product (tablet, oral), marketed as Livalo, Pitavastatin Calcium, Zypitamag and 1 more.
- Registered studies
- 18
- Lab records
- 0
- Pathogens at ≥40%
- 2 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Abnormal circulating lipid concentration
- Cardiovascular disease
- Familial hypercholesterolemia
- Hypercholesterolemia
- Hyperlipidemia
Indications ChEMBL records as approved, from FDA and DailyMed labels. Label ↗
- WHO therapeutic group
- Hmg coa reductase inhibitors
- FDA pharmacologic class
- HMG-CoA Reductase 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 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- MRSA50.8% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- E. coli27.5% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- K. pneumoniae19.0% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- M. tuberculosis66.8% 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
18registered 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 Pitavastatin 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.
- EverolimusExisting use: Adenoma sebaceum, Anaplastic astrocytoma, Angiomyolipoma and 18 more53.9% AI-predicted activityagainst E. coli50+ registered studies
- UbrogepantExisting use: Migraine disorder53.8% AI-predicted activityagainst E. coli24 registered studies
- Caspofungin AcetateExisting use: Aspergillosis, Candidemia, Candidiasis and 1 more53.7% AI-predicted activityagainst E. coli50+ registered studies
- OdevixibatExisting use: Intrahepatic cholestasis53.7% AI-predicted activityagainst E. coli13 registered studies
- PosaconazoleExisting use: Aspergillosis, Candidiasis, Coccidioidomycosis and 2 more53.6% AI-predicted activityagainst E. coli50+ registered studies
- SiponimodExisting use: Multiple sclerosis53.6% AI-predicted activityagainst E. coli33 registered studies
- LonafarnibExisting use: Hutchinson-Gilford progeria syndrome, Laminopathies, Progeria53.6% AI-predicted activityagainst E. coli39 registered studies
- Brilliant Blue GExisting use: Disclosing Agent53.4% AI-predicted activityagainst E. coli10 registered studies
- AbarelixExisting use: Neoplasm53.4% AI-predicted activityagainst E. coli5 registered studies
- CyclosporineExisting use: Conjunctivitis, Corneal disease, Eye disease and 6 more53.3% AI-predicted activityagainst E. coli50+ registered studies
- Simeprevir SodiumExisting use: Chronic hepatitis C virus infection53.2% AI-predicted activityagainst E. coliNo documented evidence found
- Ergotamine TartrateExisting use: Headache, Migraine disorder53.1% AI-predicted activityagainst E. coli10 registered studies
Registered studies
A registration describes a study; it does not establish a positive result.
A Study of LY3015014 in Participants With High Cholesterol
NCT01890967 · start 2013-06
Registered record
- Registry ID
- NCT01890967
- Conditions
- Hypercholesterolemia
- Interventions
- LY3015014; Placebo; Statin; Ezetimibe
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2013-06
- Completion
- 2014-06
- Enrolment
- 527
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHypercholesterolemiaInterventionLY3015014; Placebo; Statin; EzetimibePhasePhase 2Registry statusCompletedA Study Comparing CoQ10 Levels While Taking 3 Different Statins
NCT01660191 · start 2011-12
Registered record
- Registry ID
- NCT01660191
- Conditions
- Hypercholesterolemia
- Interventions
- Pitavastin 4mg; Atorvastatin 20mg; Rosuvastatin 5mg
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2011-12
- Completion
- 2013-10
- Enrolment
- 134
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHypercholesterolemiaInterventionPitavastin 4mg; Atorvastatin 20mg; Rosuvastatin 5mgPhasePhase 4Registry statusCompletedDrug-Drug Interaction Study to Assess the Effects of Steady State Pitavastatin 4 mg or Rosuvastatin 40 mg on Steady-State Warfarin in Healthy Adult Volunteers
NCT01178853 · start 2010-07
Registered record
- Registry ID
- NCT01178853
- Conditions
- Healthy
- Interventions
- Warfarin; Warfarin 5mg + Rosuvastatin 40 mg once daily (QD); Warfarin 5 mg + Pitavastatin 4mg once daily (QD)
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2010-07
- Completion
- 2011-04
- Enrolment
- 48
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHealthyInterventionWarfarin; Warfarin 5mg + Rosuvastatin 40 mg once daily (QD); Warfarin 5 mg + Pitavastatin 4mg once daily (QD)PhasePhase 4Registry statusCompleted