Lopinavir
FDA-approved product (capsule, oral).
- Registered studies
- 50+
- Lab records
- 0
- Pathogens at ≥40%
- 2 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- HIV infection
- HIV-1 infection
Indications ChEMBL records as approved, from FDA and DailyMed labels. Label ↗
- Anti-infective classification
- Neither a WHO ATC code nor an FDA pharmacologic class was found for it, so whether it is already an antimicrobial is not established. It needs review and is not counted as a repurposing candidate.
Repurposing investigation
Lopinavir reaches ≥40% AI-predicted activity against MRSA and M. tuberculosis, but no WHO ATC code or FDA pharmacologic class says whether it is already an antimicrobial. It needs review, so it is not counted among the repurposing candidates.
AI-predicted activity
AI prediction · nothing measured- MRSA40.2% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- E. coli37.6% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- K. pneumoniae30.8% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- M. tuberculosis53.8% 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 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 Lopinavir 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.
Dihydroartemisinin-Piperaquine in the Context of Antiretroviral Therapy
NCT04487145 · start 2020-11-23
Registered record
- Registry ID
- NCT04487145
- Conditions
- Drug-Drug Interaction; HIV Infection
- Interventions
- Dihydroartemisinin-piperaquine
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2020-11-23
- Completion
- 2022-04-11
- Enrolment
- 194
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionDrug-Drug Interaction; HIV InfectionInterventionDihydroartemisinin-piperaquinePhasePhase 4Registry statusCompletedPhase II RCT to Assess Efficacy of Intravenous Administration of Oxytocin in Patients Affected by COVID-19
NCT04386447 · start 2020-09-01
Registered record
- Registry ID
- NCT04386447
- Conditions
- Covid-19; Corona Virus Infection; SARS-CoV 2
- Interventions
- Oxytocin; Standard of Care
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Withdrawn
- Start
- 2020-09-01
- Completion
- 2020-12-31
- Enrolment
- 0
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCovid-19; Corona Virus Infection; SARS-CoV 2InterventionOxytocin; Standard of CarePhasePhase 2Registry statusWithdrawnStudy of Favipiravir Compared to Standard of Care in Hospitalized Patients With COVID-19
NCT04542694 · start 2020-05-21
Registered record
- Registry ID
- NCT04542694
- Conditions
- COVID-19
- Interventions
- Favipiravir; Standard of care
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2020-05-21
- Completion
- 2020-08-20
- Enrolment
- 200
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCOVID-19InterventionFavipiravir; Standard of carePhasePhase 3Registry statusCompletedAn Investigation Into Beneficial Effects of Interferon Beta 1a, Compared to Interferon Beta 1b And The Base Therapeutic Regiment in Moderate to Severe COVID-19: A Randomized Clinical Trial
NCT04343768 · start 2020-04-09
Registered record
- Registry ID
- NCT04343768
- Conditions
- COVID-19
- Interventions
- Hydroxychloroquine; Lopinavir / Ritonavir; Interferon Beta-1A; Interferon Beta-1B
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2020-04-09
- Completion
- 2020-04-27
- Enrolment
- 60
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCOVID-19InterventionHydroxychloroquine; Lopinavir / Ritonavir; Interferon Beta-1A; Interferon Beta-1BPhasePhase 2Registry statusCompletedCorona Virus Disease 2019 Patients Whose Nucleic Acids Changed From Negative to Positive
NCT04333589 · start 2020-04-01
Registered record
- Registry ID
- NCT04333589
- Conditions
- COVID-19
- Interventions
- Favipiravir
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Unknown
- Start
- 2020-04-01
- Completion
- 2020-09-15
- Enrolment
- 210
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCOVID-19InterventionFavipiravirPhaseNot applicableRegistry statusUnknownPharmacokinetics, Pharmacodynamics, and Safety Profile of Understudied Drugs Administered to Children Per Standard of Care (POPS)
NCT04278404 · start 2020-03-05
Registered record
- Registry ID
- NCT04278404
- Conditions
- Coronavirus Infection (COVID-19); Pulmonary Arterial Hypertension; Urinary Tract Infections in Children; Hypertension; Pain; Hyperphosphatemia; Primary Hyperaldosteronism; Edema; Hypokalemia; Heart Failure; Hemophilia; Menorrhagia; Insomnia; Pneumonia; Skin Infection; Arrythmia; Asthma in Children; Bronchopulmonary Dysplasia; Adrenal Insufficiency; Fibrinolysis; Hemorrhage; Attention Deficit Hyperactivity Disorder; Multisystem Inflammatory Syndrome in Children (MIS-C); Kawasaki Disease; Coagulation Disorder; Down Syndrome
- Interventions
- The POP02 study is collecting bodily fluid samples (i.e., whole blood, effluent samples) of children prescribed the following drugs of interest per standard of care:
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Recruiting
- Start
- 2020-03-05
- Completion
- 2026-12
- Enrolment
- 5,000
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCoronavirus Infection (COVID-19); Pulmonary Arterial Hypertension; Urinary Tract Infections in Children; Hypertension +22 moreInterventionThe POP02 study is collecting bodily fluid samples (i.e., whole blood, effluent samples) of children prescribed the following drugs of interest per standard of care:PhaseNot recordedRegistry statusRecruitingEvaluating and Comparing the Safety and Efficiency of ASC09/Ritonavir and Lopinavir/Ritonavir for Novel Coronavirus Infection
NCT04261907 · start 2020-02-11
Registered record
- Registry ID
- NCT04261907
- Conditions
- 2019-nCoV
- Interventions
- ASC09/ritonavir group; lopinavir/ritonavir group
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Terminated
- Start
- 2020-02-11
- Completion
- 2020-04-13
- Enrolment
- 6
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
Condition2019-nCoVInterventionASC09/ritonavir group; lopinavir/ritonavir groupPhaseNot applicableRegistry statusTerminatedAntiretroviral Treatment Taken 4 Days Per Week Versus Continuous Therapy 7/7 Days Per Week in HIV-1 Infected Patients
NCT03256422 · start 2017-09-07
Registered record
- Registry ID
- NCT03256422
- Conditions
- HIV Infections
- Interventions
- Treatment discontinuation
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2017-09-07
- Completion
- 2020-03-02
- Enrolment
- 640
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHIV InfectionsInterventionTreatment discontinuationPhasePhase 3Registry statusCompletedThe Effectiveness of Dual Therapy (Lopinavir/Ritonavir + LamivudinE) in Treatment-Experienced HIV Infected Patients in the Russian Federation
NCT02581202 · start 2015-12-21
Registered record
- Registry ID
- NCT02581202
- Conditions
- HIV-1 Infection
- Interventions
- lopinavir/ritonavir; lamivudine
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2015-12-21
- Completion
- 2017-05-27
- Enrolment
- 216
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHIV-1 InfectionInterventionlopinavir/ritonavir; lamivudinePhaseNot recordedRegistry statusCompletedSafety and Efficacy of Switching From Regimens of ABC/3TC + a 3rd Agent to E/C/F/TAF Fixed-Dose Combination (FDC) in Virologically-Suppressed HIV 1 Infected Adults
NCT02605954 · start 2015-11-18
Registered record
- Registry ID
- NCT02605954
- Conditions
- HIV-1 Infection
- Interventions
- E/C/F/TAF; ABC/3TC; Third Antiretroviral Agent
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2015-11-18
- Completion
- 2018-01-24
- Enrolment
- 275
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHIV-1 InfectionInterventionE/C/F/TAF; ABC/3TC; Third Antiretroviral AgentPhasePhase 3Registry statusCompletedIMPAACT P1092: Steady State PK in Malnourished HIV Infected Children
NCT01818258 · start 2015-10-26
Registered record
- Registry ID
- NCT01818258
- Conditions
- HIV Positive; Malnourished
- Interventions
- ZDV+3TC+LPV/r
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2015-10-26
- Completion
- 2017-09-29
- Enrolment
- 52
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHIV Positive; MalnourishedInterventionZDV+3TC+LPV/rPhasePhase 4Registry statusCompletedProspective Study of Lopinavir Based ART for HIV Infected childreN Globally (LIVING Study)
NCT02346487 · start 2015-09
Registered record
- Registry ID
- NCT02346487
- Conditions
- HIV
- Interventions
- LPV/RTV pellets and AZT/3TC or ABC/3TC
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2015-09
- Completion
- 2019-05-14
- Enrolment
- 1,003
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHIVInterventionLPV/RTV pellets and AZT/3TC or ABC/3TCPhasePhase 3Registry statusCompletedHIV Reservoir Dynamics After Switching to Dolutegravir in Patients on a PI and 2 NRTI Based Regimen
NCT02513147 · start 2015-06
Registered record
- Registry ID
- NCT02513147
- Conditions
- HIV-1
- Interventions
- Dolutegravir; PI; 2 NRTI; 2 NRTI
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2015-06
- Completion
- 2016-11
- Enrolment
- 44
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHIV-1InterventionDolutegravir; PI; 2 NRTI; 2 NRTIPhasePhase 4Registry statusCompletedVery Early Intensive Treatment of Infants Living With HIV to Achieve HIV Remission
NCT02140255 · start 2015-01-23
Registered record
- Registry ID
- NCT02140255
- Conditions
- HIV Infection
- Interventions
- Nucleoside Reverse Transcriptase Inhibitors (NRTIs); Nevirapine (NVP); Lopinavir/Ritonavir (LPV/r); Raltegravir (RAL); VRC01; Dolutegravir (DTG); VRC07-523LS
- Study type
- INTERVENTIONAL
- Phase
- Phase 1 / Phase 2
- Registry status
- Recruiting
- Start
- 2015-01-23
- Completion
- 2031-12-31
- Enrolment
- 1,120
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHIV InfectionInterventionNucleoside Reverse Transcriptase Inhibitors (NRTIs); Nevirapine (NVP); Lopinavir/Ritonavir (LPV/r); Raltegravir (RAL) +3 morePhasePhase 1 / Phase 2Registry statusRecruitingTrial to Evaluate the Interest of a Reductive Anti Retroviral Strategy Using Dual Therapy Inspite of Triple Therapy
NCT02302547 · start 2014-12
Registered record
- Registry ID
- NCT02302547
- Conditions
- HIV
- Interventions
- triple therapy; dual therapy
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2014-12
- Completion
- 2018-09-21
- Enrolment
- 224
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHIVInterventiontriple therapy; dual therapyPhasePhase 3Registry statusCompleted