Minoxidil
FDA-approved product (tablet, oral), marketed as Loniten, Men's Rogaine, Minodyl and 9 more.
- Registered studies
- 50+
- Lab records
- 0
- Pathogens at ≥40%
- 1 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Alopecia
- Androgenetic alopecia
- Hypertension
- Hypotrichosis
Indications ChEMBL records as approved, from FDA and DailyMed labels. Label ↗
- WHO therapeutic group
- Pyrimidine derivatives; Other dermatologicals
- FDA pharmacologic class
- Arteriolar Vasodilator 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 M. tuberculosis. It was surfaced computationally for further investigation; it is not an established treatment for this infection.
AI-predicted activity
AI prediction · nothing measured- MRSA29.0% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- E. coli28.0% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- K. pneumoniae11.0% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- M. tuberculosis58.0% 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 Minoxidil 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.
Minoxidil With or Without Low-Level Red-Light Therapy for Improving Chemotherapy-Induced Alopecia in Breast Cancer Patients
NCT07594678 · start 2026-11-15
Registered record
- Registry ID
- NCT07594678
- Conditions
- Anatomic Stage I Breast Cancer AJCC v8; Anatomic Stage II Breast Cancer AJCC v8; Anatomic Stage III Breast Cancer AJCC v8; Anatomic Stage IV Breast Cancer AJCC v8; Chemotherapy-Induced Alopecia
- Interventions
- Electronic Health Record Review; Minoxidil; Revian RED LED-light cap; Survey Administration
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Not yet recruiting
- Start
- 2026-11-15
- Completion
- 2027-12-31
- Enrolment
- 50
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAnatomic Stage I Breast Cancer AJCC v8; Anatomic Stage II Breast Cancer AJCC v8; Anatomic Stage III Breast Cancer AJCC v8; Anatomic Stage IV Breast Cancer AJCC v8 +1 moreInterventionElectronic Health Record Review; Minoxidil; Revian RED LED-light cap; Survey AdministrationPhasePhase 2Registry statusNot yet recruitingFor an Investigator-led Hair Study Comparing Between Healthy and Hair Loss Volunteers
NCT07716748 · start 2026-08
Registered record
- Registry ID
- NCT07716748
- Conditions
- Hair Loss
- Interventions
- Not recorded
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Not yet recruiting
- Start
- 2026-08
- Completion
- 2028-01
- Enrolment
- 66
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHair LossInterventionNot recordedPhaseNot recordedRegistry statusNot yet recruitingVENEZE Peptide Factor Hair Serum Compared With Topical 2% Minoxidil for Androgenetic Alopecia
NCT07536100 · start 2026-05-05
Registered record
- Registry ID
- NCT07536100
- Conditions
- Androgenetic Alopecia (AGA)
- Interventions
- Veneze peptide hair serum; Topical minoxidil
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Recruiting
- Start
- 2026-05-05
- Completion
- 2026-11-30
- Enrolment
- 80
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAndrogenetic Alopecia (AGA)InterventionVeneze peptide hair serum; Topical minoxidilPhaseNot applicableRegistry statusRecruitingAndrogenic Alopecia TH07 Clinical Trial
NCT07435012 · start 2026-04
Registered record
- Registry ID
- NCT07435012
- Conditions
- Androgenic Alopecia
- Interventions
- TH07; TH07; Minoxidil 5% Topical Solution; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Recruiting
- Start
- 2026-04
- Completion
- 2028-04
- Enrolment
- 420
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAndrogenic AlopeciaInterventionTH07; TH07; Minoxidil 5% Topical Solution; PlaceboPhasePhase 3Registry statusRecruitingEffects of a Topical Serum Solution on Hair Characteristics
NCT07785869 · start 2026-01-26
Registered record
- Registry ID
- NCT07785869
- Conditions
- Hair Characteristics
- Interventions
- Re:You Hair Revival Serum 1; Re:You Hair Revival Serum 2; Topical Minoxidil 2%
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Active not recruiting
- Start
- 2026-01-26
- Completion
- 2026-09-25
- Enrolment
- 190
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHair CharacteristicsInterventionRe:You Hair Revival Serum 1; Re:You Hair Revival Serum 2; Topical Minoxidil 2%PhaseNot applicableRegistry statusActive not recruitingTopical Application of Lactobacillus Reuteri for Androgenetic Alopecia
NCT07370519 · start 2026-01-25
Registered record
- Registry ID
- NCT07370519
- Conditions
- Androgenetic Alopecia (AGA)
- Interventions
- Lactobacillus reuteri; Inactivated Lactobacillus reuteri; 5% Minoxidil; Normal Saline
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Recruiting
- Start
- 2026-01-25
- Completion
- 2027-06
- Enrolment
- 388
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAndrogenetic Alopecia (AGA)InterventionLactobacillus reuteri; Inactivated Lactobacillus reuteri; 5% Minoxidil; Normal SalinePhasePhase 2Registry statusRecruitingTopical 2-Deoxy-D-ribose Hydrogel Versus Minoxidil 5% Solution for Androgenetic Alopecia
NCT07502976 · start 2026-01-01
Registered record
- Registry ID
- NCT07502976
- Conditions
- Androgenic Alopecia
- Interventions
- Topical 2-Deoxy-D-ribose Hydrogel; Topical Minoxidil 5% Solution
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Recruiting
- Start
- 2026-01-01
- Completion
- 2027-01
- Enrolment
- 60
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAndrogenic AlopeciaInterventionTopical 2-Deoxy-D-ribose Hydrogel; Topical Minoxidil 5% SolutionPhaseNot applicableRegistry statusRecruitingComparison of Outcomes Between Topical Minoxidil Versus Oral Minoxidil for the Treatment of Androgenetic Alopecia
NCT07273799 · start 2025-12-20
Registered record
- Registry ID
- NCT07273799
- Conditions
- Androgenic Alopecia
- Interventions
- Minoxidil 5 % Topical Spray; minoxidil; Placebo Spray; Placebo Tablet or Capsule
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Not yet recruiting
- Start
- 2025-12-20
- Completion
- 2026-06-01
- Enrolment
- 200
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAndrogenic AlopeciaInterventionMinoxidil 5 % Topical Spray; minoxidil; Placebo Spray; Placebo Tablet or CapsulePhasePhase 3Registry statusNot yet recruitingEffect of Minoxidil Solution Iontophoresis on Androgenic Alopecia
NCT07056933 · start 2025-07-08
Registered record
- Registry ID
- NCT07056933
- Conditions
- Alopecia
- Interventions
- Minoxidil solution iontophoresis; saline solution iontophoresis
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Not yet recruiting
- Start
- 2025-07-08
- Completion
- 2025-11-30
- Enrolment
- 25
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAlopeciaInterventionMinoxidil solution iontophoresis; saline solution iontophoresisPhaseNot applicableRegistry statusNot yet recruitingLow Dose Oral Minoxdil in Androgenic Alopecia
NCT07018349 · start 2025-06-15
Registered record
- Registry ID
- NCT07018349
- Conditions
- Androgenetic Alopecia (AGA)
- Interventions
- 2.5% Oral minoxidil; 1% Oral Minoxidil
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Not yet recruiting
- Start
- 2025-06-15
- Completion
- 2025-10-20
- Enrolment
- 76
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAndrogenetic Alopecia (AGA)Intervention2.5% Oral minoxidil; 1% Oral MinoxidilPhaseNot applicableRegistry statusNot yet recruitingEfficacy of Dihydroartemisinin for Treating Female Androgenetic Alopecia
NCT07012486 · start 2025-06
Registered record
- Registry ID
- NCT07012486
- Conditions
- Androgenetic Alopecia (AGA)
- Interventions
- Oral DHA + Topical minoxidil 5%; Topical Minoxidil 5%
- Study type
- INTERVENTIONAL
- Phase
- Early phase 1
- Registry status
- Recruiting
- Start
- 2025-06
- Completion
- 2026-12
- Enrolment
- 30
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAndrogenetic Alopecia (AGA)InterventionOral DHA + Topical minoxidil 5%; Topical Minoxidil 5%PhaseEarly phase 1Registry statusRecruitingMinoxidil for Treating White Hair: A Randomized Controlled Trial
NCT06813963 · start 2025-02-15
Registered record
- Registry ID
- NCT06813963
- Conditions
- Grey Hair
- Interventions
- Topical Minoxidil(5%) to the scalp.; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2025-02-15
- Completion
- 2026-03-15
- Enrolment
- 141
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionGrey HairInterventionTopical Minoxidil(5%) to the scalp.; PlaceboPhasePhase 4Registry statusCompletedVarious Procedural Treatment Options for Androgenetic Alopecia
NCT06826001 · start 2025-02
Registered record
- Registry ID
- NCT06826001
- Conditions
- Androgenetic Alopecia
- Interventions
- topical finasteride; Topical minoxidil
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Not yet recruiting
- Start
- 2025-02
- Completion
- 2025-07
- Enrolment
- 190
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAndrogenetic AlopeciaInterventiontopical finasteride; Topical minoxidilPhasePhase 2Registry statusNot yet recruitingClinical Study of PRP in the Treatment of Androgenetic Alopecia
NCT07551271 · start 2025-01-01
Registered record
- Registry ID
- NCT07551271
- Conditions
- Androgenetic Alopecia (AGA)
- Interventions
- PRP
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2025-01-01
- Completion
- 2026-03-01
- Enrolment
- 30
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAndrogenetic Alopecia (AGA)InterventionPRPPhaseNot applicableRegistry statusCompletedProof-of-Science, Prospective, Interventional, Three-arm, Double-Blind, Randomized, Safety and Efficacy Real World Evidence Study.
NCT06552039 · start 2024-12-26
Registered record
- Registry ID
- NCT06552039
- Conditions
- Hair Fall and Pre-mature Graying
- Interventions
- Polyherbal Hair Oil; Minoxidil Herbal Hair Oil + Minoxidil 5 (%) Hair Serum; Minoxidil Hair Serum
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2024-12-26
- Completion
- 2025-06-28
- Enrolment
- 99
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHair Fall and Pre-mature GrayingInterventionPolyherbal Hair Oil; Minoxidil Herbal Hair Oil + Minoxidil 5 (%) Hair Serum; Minoxidil Hair SerumPhaseNot applicableRegistry statusCompleted