Penicillin V
FDA-approved product (for suspension, oral), marketed as V-Cillin, Beepen-Vk, Betapen-Vk and 12 more.
- Registered studies
- 30
- Lab records
- 10
- Pathogens at ≥40%
- 1 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Arthritis
- Bacterial disease
- Bacterial endocarditis
- Bacteriemia
- Infection
- Infectious meningitis
- Scarlet fever
Indications ChEMBL records as approved, from FDA and DailyMed labels. Label ↗
- WHO therapeutic group
- Beta-lactamase sensitive penicillins
- Anti-infective classification
- Classified as an existing antimicrobial.WHO ATC J01CE02; WHO ATC J01CE10
Repurposing investigation
Penicillin V is already an antimicrobial, so it is not counted among the repurposing candidates. Its AI-predicted activity is shown below for reference.
AI-predicted activity
AI prediction · nothing measured- MRSA76.0% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates. This medicine was in the model's training data, so this is recall, not a new prediction.
- E. coli5.1% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates. This medicine was in the model's training data, so this is recall, not a new prediction.
- K. pneumoniae4.8% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates. This medicine was in the model's training data, so this is recall, not a new prediction.
- M. tuberculosis33.4% AI-predicted activityBelow 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
30registered studies name this medicine, for any condition. See them below.
Experimental
- MRSA: measured active in 2 of 3 lab records
- E. coli: measured active in 0 of 4 lab records
- K. pneumoniae: measured active in 0 of 3 lab records
Show the 10 laboratory records, with sources
Loading records…
“Active” means the measured value reached this project’s laboratory cutoff (10 µM or stronger). A laboratory result does not show an effect in patients.
Docking
Computational · nothing measuredAutoDock 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 Penicillin V 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.
Penicillin to Prevent Early Rheumatic Heart Disease in School-Aged Children
NCT07798232 · start 2027-02-01
Registered record
- Registry ID
- NCT07798232
- Conditions
- Rheumatic Heart Disease in Children
- Interventions
- Oral Penicillin V
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Not yet recruiting
- Start
- 2027-02-01
- Completion
- 2032-03-01
- Enrolment
- 9,622
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionRheumatic Heart Disease in ChildrenInterventionOral Penicillin VPhasePhase 3Registry statusNot yet recruitingProphylaxis of Recurrent Erysipelas in Lower Limbs: compreSsion thErapy vs aNTibiotics and Compression Therapy.
NCT07549594 · start 2026-04-01
Registered record
- Registry ID
- NCT07549594
- Conditions
- Recurrent Erysipelas
- Interventions
- elastic stockings; Phenoxymethylpenicillin
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Not yet recruiting
- Start
- 2026-04-01
- Completion
- 2030-04-01
- Enrolment
- 200
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionRecurrent ErysipelasInterventionelastic stockings; PhenoxymethylpenicillinPhasePhase 4Registry statusNot yet recruitingThe Optimal Antibiotic Treatment Duration for Community-acquired Pneumonia in Adults Diagnosed in General Practice in Denmark (CAP-D)
NCT06295120 · start 2023-11-13
Registered record
- Registry ID
- NCT06295120
- Conditions
- Community-acquired Pneumonia
- Interventions
- Phenoxymethylpenicillin 1.2 MIE 4 times daily
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Recruiting
- Start
- 2023-11-13
- Completion
- 2026-03-31
- Enrolment
- 600
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCommunity-acquired PneumoniaInterventionPhenoxymethylpenicillin 1.2 MIE 4 times dailyPhasePhase 4Registry statusRecruitingGOALIE: Intramuscular vs. Enteral Penicillin Prophylaxis to Prevent Progression of Latent RHD Trial
NCT05693545 · start 2023-09-01
Registered record
- Registry ID
- NCT05693545
- Conditions
- Rheumatic Heart Disease
- Interventions
- phenoxymethyl penicillin; intramuscular benzathine penicillin G (BPG) prophylaxis
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Active not recruiting
- Start
- 2023-09-01
- Completion
- 2027-09-30
- Enrolment
- 1,004
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionRheumatic Heart DiseaseInterventionphenoxymethyl penicillin; intramuscular benzathine penicillin G (BPG) prophylaxisPhasePhase 2Registry statusActive not recruitingAddition of Probenecid to Penicillin-V Therapy
NCT05082909 · start 2021-12-21
Registered record
- Registry ID
- NCT05082909
- Conditions
- Infection, Bacterial
- Interventions
- Probenecid
- Study type
- INTERVENTIONAL
- Phase
- Phase 1 / Phase 2
- Registry status
- Completed
- Start
- 2021-12-21
- Completion
- 2022-07-07
- Enrolment
- 21
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionInfection, BacterialInterventionProbenecidPhasePhase 1 / Phase 2Registry statusCompletedEffects of Phenoximethylpenicillin, Amoxicillin and Amoxicillin-clavulanic Acid on the Gut Microbiota
NCT04084106 · start 2019-09-10
Registered record
- Registry ID
- NCT04084106
- Conditions
- Infectious Disease
- Interventions
- Phenoxymethylpenicillin; Amoxicillin; Amoxicillin-clavulanic acid
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2019-09-10
- Completion
- 2022-11-11
- Enrolment
- 104
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionInfectious DiseaseInterventionPhenoxymethylpenicillin; Amoxicillin; Amoxicillin-clavulanic acidPhasePhase 4Registry statusCompletedSore Throat in Primary Care - a Comparison of Phenoxymethylpenicillin and No Antibiotic Treatment
NCT04083417 · start 2019-09-09
Registered record
- Registry ID
- NCT04083417
- Conditions
- Sore Throat; Tonsillitis
- Interventions
- Phenoxymethylpenicillin; No antibiotic treatment
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Recruiting
- Start
- 2019-09-09
- Completion
- 2026-06
- Enrolment
- 260
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSore Throat; TonsillitisInterventionPhenoxymethylpenicillin; No antibiotic treatmentPhasePhase 4Registry statusRecruitingMinimally Invasive Sensing of Beta-lactam Antibiotics
NCT03847610 · start 2018-04-12
Registered record
- Registry ID
- NCT03847610
- Conditions
- Healthy Volunteers
- Interventions
- Phenoxymethyl Penicillin; Microneedle array
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2018-04-12
- Completion
- 2018-08-10
- Enrolment
- 11
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHealthy VolunteersInterventionPhenoxymethyl Penicillin; Microneedle arrayPhasePhase 1Registry statusCompletedPeritonsillar Abscess: Aspiration Versus Tonsillectomy a Chaud
NCT03326661 · start 2017-11-10
Registered record
- Registry ID
- NCT03326661
- Conditions
- Peritonsillar Abscess
- Interventions
- Aspiration; Tonsillectomy a chaud; Penicillin V + metronidazol (Penicillin allergy: Clindamycin alone)
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Unknown
- Start
- 2017-11-10
- Completion
- 2020-11-30
- Enrolment
- 128
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPeritonsillar AbscessInterventionAspiration; Tonsillectomy a chaud; Penicillin V + metronidazol (Penicillin allergy: Clindamycin alone)PhaseNot applicableRegistry statusUnknownPenicillin for the Emergency Department Outpatient Treatment of CELLulitis
NCT02922686 · start 2016-12
Registered record
- Registry ID
- NCT02922686
- Conditions
- Cellulitis; Wound Infection; Abscess
- Interventions
- Flucloxacillin; Phenoxymethylpenicillin; Placebo (for phenoxymethylpenicillin)
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Unknown
- Start
- 2016-12
- Completion
- 2019-12
- Enrolment
- 414
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCellulitis; Wound Infection; AbscessInterventionFlucloxacillin; Phenoxymethylpenicillin; Placebo (for phenoxymethylpenicillin)PhasePhase 4Registry statusUnknownZinc Supplementation in Children With Sickle Cell Disease in Western Kenya
NCT03293641 · start 2016-05-20
Registered record
- Registry ID
- NCT03293641
- Conditions
- Sickle Cell Disease; Zinc Deficiency; Infection
- Interventions
- Zinc Sulfate Tablets; Standard of Care
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2016-05-20
- Completion
- 2017-01-19
- Enrolment
- 40
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSickle Cell Disease; Zinc Deficiency; InfectionInterventionZinc Sulfate Tablets; Standard of CarePhaseNot applicableRegistry statusCompletedStudy of 5 and 10 Days Treatment With Penicillin Against Sore Throat Caused by Streptococci
NCT02712307 · start 2015-09
Registered record
- Registry ID
- NCT02712307
- Conditions
- Tonsillitis
- Interventions
- Phenoxymethylpenicillin
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2015-09
- Completion
- 2018-06
- Enrolment
- 433
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionTonsillitisInterventionPhenoxymethylpenicillinPhasePhase 4Registry statusCompletedSurgical Treatment of Peri-implantitis With and Without Systemically Adjunctive Antibiotics
NCT02185209 · start 2015-03
Registered record
- Registry ID
- NCT02185209
- Conditions
- Periodontal Diseases; Periimplantitis
- Interventions
- Placebo; Amoxicillin Sandoz; Metronidazole Sanofi; Phenoxymethylpenicillin Meda
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2015-03
- Completion
- 2022-05-27
- Enrolment
- 77
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPeriodontal Diseases; PeriimplantitisInterventionPlacebo; Amoxicillin Sandoz; Metronidazole Sanofi; Phenoxymethylpenicillin MedaPhasePhase 4Registry statusCompletedEfficacy of Oral Antibiotic Therapy Compared to Intravenous Antibiotic Therapy for Osteomyelitis
NCT02168816 · start 2014-03-19
Registered record
- Registry ID
- NCT02168816
- Conditions
- Osteomyelitis
- Interventions
- Intravenous Antibacterial Agent; Oral Antibacterial Agent
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Terminated
- Start
- 2014-03-19
- Completion
- 2017-02-02
- Enrolment
- 30
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionOsteomyelitisInterventionIntravenous Antibacterial Agent; Oral Antibacterial AgentPhasePhase 2Registry statusTerminatedPatients Response to Early Switch To Oral:Osteomyelitis Study
NCT02099240 · start 2014-03-06
Registered record
- Registry ID
- NCT02099240
- Conditions
- Osteomyelitis
- Interventions
- oral antibiotics; intravenous antibiotics
- Study type
- INTERVENTIONAL
- Phase
- Early phase 1
- Registry status
- Terminated
- Start
- 2014-03-06
- Completion
- 2018-11-07
- Enrolment
- 11
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionOsteomyelitisInterventionoral antibiotics; intravenous antibioticsPhaseEarly phase 1Registry statusTerminated