Permethrin
FDA-approved product (lotion, topical), marketed as Elimite, Nix, Permethrin.
- Registered studies
- 50+
- Lab records
- 0
- Pathogens at ≥40%
- 2 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Parasitic infection
Indications ChEMBL records as approved, from FDA and DailyMed labels.
- WHO therapeutic group
- Pyrethrines, incl. synthetic compounds
- FDA pharmacologic class
- Pyrethroid FDA label ↗
- Anti-infective classification
- Classified as another kind of anti-infective (for example an antifungal, antiviral or antiparasitic medicine).WHO ATC P03AC04; WHO ATC P03AC54
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- MRSA41.0% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- E. coli31.6% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- K. pneumoniae13.6% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- M. tuberculosis48.4% 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 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 Permethrin 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.
Safety, Efficacy and Preventative Effect of a Head Lice Product (X92001483) vs. Nix Creme Rinse (1% Permethrin).
NCT07660354 · start 2026-05-01
Registered record
- Registry ID
- NCT07660354
- Conditions
- Lice; Head Lice
- Interventions
- Medical Device (X92001483)
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Recruiting
- Start
- 2026-05-01
- Completion
- 2026-12
- Enrolment
- 98
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionLice; Head LiceInterventionMedical Device (X92001483)PhaseNot applicableRegistry statusRecruitingComparison of Permethrin-Based Treatment Strategies Against Scabies in Infants and Young Children
NCT07247630 · start 2026-01-15
Registered record
- Registry ID
- NCT07247630
- Conditions
- Scabies
- Interventions
- Permethrin 5%
- Study type
- INTERVENTIONAL
- Phase
- Early phase 1
- Registry status
- Not yet recruiting
- Start
- 2026-01-15
- Completion
- 2026-06-15
- Enrolment
- 68
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionScabiesInterventionPermethrin 5%PhaseEarly phase 1Registry statusNot yet recruitingLong-term Follow-up of Children Born in the PETN Studies
NCT06534307 · start 2024-06-01
Registered record
- Registry ID
- NCT06534307
- Conditions
- Intrauterine Growth Restriction; Pentaerithrityl Teratnitrate in Pregnancy; Long-Term Effects to Children
- Interventions
- Questionnaire Child Behaviour Checklist; Questionnaire Young Self Report; physical examination; metabolic examination; Questionnaire Reynolds Intellectual Assessment Scales and Screening; electroencephalogram; Questionnaire Movement Assessment Battery for Children; Questionnaire Continuous Performance Test; Questionnaire Diagnostic System for Mental Disorders; kidney function tests; Questionnaire Five to Fifteen; cardiovacular examination
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Recruiting
- Start
- 2024-06-01
- Completion
- 2028-03-31
- Enrolment
- 228
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionIntrauterine Growth Restriction; Pentaerithrityl Teratnitrate in Pregnancy; Long-Term Effects to ChildrenInterventionQuestionnaire Child Behaviour Checklist; Questionnaire Young Self Report; physical examination; metabolic examination +8 morePhaseNot recordedRegistry statusRecruitingSulfur 7% Cream Compared With Permethrin 5% Cream for Treating Scabies in Adults
NCT07822672 · start 2024-06-01
Registered record
- Registry ID
- NCT07822672
- Conditions
- Scabies
- Interventions
- Sulfur 7% cream; Permethrin 5% cream
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2024-06-01
- Completion
- 2026-06-01
- Enrolment
- 90
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionScabiesInterventionSulfur 7% cream; Permethrin 5% creamPhasePhase 4Registry statusCompletedComparison Effectiveness of Oral Ivermectin , 1% Permethrin Shampoo and 4% Dimeticone Liquid Gel in the Treatment of Pediculosis Capitis Among School Children in Chachoengsao Province, Thailand
NCT06332872 · start 2023-12-15
Registered record
- Registry ID
- NCT06332872
- Conditions
- Pediculus Capitis Infestation; Permethrin Adverse Reaction; Dimethicone Adverse Reaction; Permethrin Allergy; Dimethicone Allergy; Ivermectin; School-age Children
- Interventions
- Oral Ivermectin; 4% dimenticone liquid gel
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Unknown
- Start
- 2023-12-15
- Completion
- 2024-05
- Enrolment
- 117
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPediculus Capitis Infestation; Permethrin Adverse Reaction; Dimethicone Adverse Reaction; Permethrin Allergy +3 moreInterventionOral Ivermectin; 4% dimenticone liquid gelPhasePhase 4Registry statusUnknownIvermectin Safety in Small Children
NCT04332068 · start 2023-11-18
Registered record
- Registry ID
- NCT04332068
- Conditions
- Scabies
- Interventions
- Oral ivermectin; Permethrin Cream; Placebo tablet; Placebo cream
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2023-11-18
- Completion
- 2025-04-04
- Enrolment
- 240
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionScabiesInterventionOral ivermectin; Permethrin Cream; Placebo tablet; Placebo creamPhasePhase 2Registry statusCompletedIvermectin/ Permethrin for Scabies
NCT05819983 · start 2023-01-25
Registered record
- Registry ID
- NCT05819983
- Conditions
- Scabies
- Interventions
- Ivermectin Tablets; Permethrin Cream
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2023-01-25
- Completion
- 2023-03-06
- Enrolment
- 60
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionScabiesInterventionIvermectin Tablets; Permethrin CreamPhasePhase 4Registry statusCompletedA Study to Evaluate the Efficacy and Safety of a Leave-in Spray in Subjects With Head Lice Infestation
NCT05565820 · start 2022-12-15
Registered record
- Registry ID
- NCT05565820
- Conditions
- Pediculosis Capitis; Lice Infestations; Head Lice
- Interventions
- Vamousse Spray 'n' Go; Nix Creme Rinse Lice Treatment
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2022-12-15
- Completion
- 2023-03-12
- Enrolment
- 58
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPediculosis Capitis; Lice Infestations; Head LiceInterventionVamousse Spray 'n' Go; Nix Creme Rinse Lice TreatmentPhasePhase 4Registry statusCompletedBortezomib and Pembrolizumab With or Without Pelareorep for the Treatment of Relapsed or Refractory Multiple Myeloma, AMBUSH Trial
NCT05514990 · start 2022-10-07
Registered record
- Registry ID
- NCT05514990
- Conditions
- Recurrent Plasma Cell Myeloma; Refractory Plasma Cell Myeloma
- Interventions
- Bortezomib; Dexamethasone; Pelareorep; Pembrolizumab
- Study type
- INTERVENTIONAL
- Phase
- Phase 1 / Phase 2
- Registry status
- Active not recruiting
- Start
- 2022-10-07
- Completion
- 2027-08-22
- Enrolment
- 10
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionRecurrent Plasma Cell Myeloma; Refractory Plasma Cell MyelomaInterventionBortezomib; Dexamethasone; Pelareorep; PembrolizumabPhasePhase 1 / Phase 2Registry statusActive not recruitingPermethrin-treated Baby-wraps for the Prevention of Malaria in Children
NCT05391230 · start 2022-06-03
Registered record
- Registry ID
- NCT05391230
- Conditions
- Malaria; P. Falciparum
- Interventions
- Permethrin-treated lesu; Untreated lesu
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2022-06-03
- Completion
- 2024-11-30
- Enrolment
- 400
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMalaria; P. FalciparumInterventionPermethrin-treated lesu; Untreated lesuPhaseNot applicableRegistry statusCompletedAutoMated BUrn Diagnostic System for Healthcare (AMBUSH)
NCT05167461 · start 2022-05-24
Registered record
- Registry ID
- NCT05167461
- Conditions
- Burns Multiple; Burns; Thermal Burn; Burn Infection
- Interventions
- Collection of imaging by ultrasonography
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2022-05-24
- Completion
- 2023-05-25
- Enrolment
- 30
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionBurns Multiple; Burns; Thermal Burn; Burn InfectionInterventionCollection of imaging by ultrasonographyPhaseNot recordedRegistry statusCompletedSulfur vs. Different Regimes of Permethrin for Scabies
NCT06396507 · start 2022-03-15
Registered record
- Registry ID
- NCT06396507
- Conditions
- Scabies
- Interventions
- Permethrin Solution; Sulfur
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2022-03-15
- Completion
- 2022-11-12
- Enrolment
- 250
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionScabiesInterventionPermethrin Solution; SulfurPhasePhase 3Registry statusCompletedComparison of Oral Ivermectin and Permethrin 5% Lotion in Treatment of Pediculosis Capitis
NCT05643820 · start 2022-03-01
Registered record
- Registry ID
- NCT05643820
- Conditions
- Pediculosis
- Interventions
- Permethrin 5% topical lotion; Ivermectin
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2022-03-01
- Completion
- 2022-08-31
- Enrolment
- 60
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPediculosisInterventionPermethrin 5% topical lotion; IvermectinPhasePhase 1Registry statusCompletedComparison of Topical 5% Permethrin and Topical 10% Sulfur in the Treatment of Scabies
NCT05862701 · start 2022-03-01
Registered record
- Registry ID
- NCT05862701
- Conditions
- Scabies
- Interventions
- Permethrin; Sulphur
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2022-03-01
- Completion
- 2022-09-30
- Enrolment
- 60
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionScabiesInterventionPermethrin; SulphurPhasePhase 1Registry statusCompletedA Clinical Trial to Evaluate Efficacy and Safety of a New Suffocating Head Lice Product.
NCT05378477 · start 2022-01-17
Registered record
- Registry ID
- NCT05378477
- Conditions
- Head Lice; Pediculosis Capitis
- Interventions
- X92001752; RID Super Max Solution; Nix Crème; Pouxit Végétal
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Unknown
- Start
- 2022-01-17
- Completion
- 2022-09-30
- Enrolment
- 220
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHead Lice; Pediculosis CapitisInterventionX92001752; RID Super Max Solution; Nix Crème; Pouxit VégétalPhaseNot applicableRegistry statusUnknown