Methotrexate
FDA-approved product (solution, subcutaneous), marketed as Jylamvo, Methotrexate, Otrexup and 15 more.
- Registered studies
- 50+
- Lab records
- 22
- Pathogens at ≥40%
- 3 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Acute lymphoblastic leukemia
- Adenoma
- Arthritis
- B-cell acute lymphoblastic leukemia
- Breast cancer
- Breast carcinoma
- Breast neoplasm
- Cancer
- Childhood acute lymphoblastic leukemia
- Choriocarcinoma
- Fungal infectious disease
- Immune system disease
- Juvenile idiopathic arthritis
- Leptomeningeal metastasis
- Lung cancer
- Lymphoblastic lymphoma
- and 8 more
Indications ChEMBL records as approved, from FDA and DailyMed labels. Label ↗
- WHO therapeutic group
- Folic acid analogues; Other immunosuppressants
- FDA pharmacologic class
- Folate Analog Metabolic 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 E. coli, 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- MRSA64.1% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- E. coli86.8% 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.
- K. pneumoniae27.8% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- M. tuberculosis68.1% 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
- E. coli: measured active in 21 of 22 lab records
Show the 22 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 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 Methotrexate 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.
- Trimetrexate GlucuronateExisting use: Other agents against amoebiasis and other protozoal diseases88.6% AI-predicted activityagainst E. coliLab records exist17 registered studies
- Folic AcidExisting use: Acne, Anemia, Anemia (phenotype) and 8 more87.0% AI-predicted activityagainst E. coliLab records exist50+ registered studies
- PralatrexateExisting use: Cancer, Mature T-cell and NK-cell non-Hodgkin lymphoma, Neoplasm and 2 more82.2% AI-predicted activityagainst E. coli44 registered studies
- TriclosanExisting use: Phenol and derivatives, Medicated dressings with antiinfectives81.0% AI-predicted activityagainst E. coliLab records exist50+ registered studies
- Leucovorin CalciumExisting use: Osteosarcoma67.6% AI-predicted activityagainst E. coli50+ registered studies
- LevoleucovorinExisting use: Anemia, Colorectal adenocarcinoma, Colorectal cancer and 3 more67.6% AI-predicted activityagainst E. coli50+ registered studies
- PyrimethamineExisting use: Malaria, Toxoplasmosis64.6% AI-predicted activityagainst E. coliLab records exist50+ registered studies
- Copanlisib DihydrochlorideExisting use: Follicular lymphoma, Neoplasm, Neoplasm of mature B-cells63.5% AI-predicted activityagainst E. coli10 registered studies
- AfamelanotideExisting use: Erythropoietic protoporphyria62.6% AI-predicted activityagainst E. coli23 registered studies
- Rimegepant SulfateExisting use: Migraine disorder61.6% AI-predicted activityagainst E. coli50+ registered studies
- Histrelin AcetateExisting use: Neoplasm, Prostate adenocarcinoma, Prostate cancer61.6% AI-predicted activityagainst E. coli13 registered studies
- Pafolacianine SodiumExisting use: Other diagnostic agents61.4% AI-predicted activityagainst E. coli1 registered study
Registered studies
A registration describes a study; it does not establish a positive result.
Utilization of a Microdevice for Psoriasis and Atopic Dermatitis
NCT07352566 · start 2026-08-01
Registered record
- Registry ID
- NCT07352566
- Conditions
- Psoriasis; Atopic Dermatitis
- Interventions
- In situ cutaneous microdevice; Triamcinolone; 5-Fluorouracil; Calcipotriene; Tapinarof; Crisaborole; Tacrolimus; Adalimumab; Etanercept; Certolizumab; Infliximab; Secukinumab; Ixekizumab; Apremilast; Risankizumab; Ustekinumab; Hydroxychloroquine; Methotrexate; Mycophenolate; Azathioprine; Chloroquine; Cyclosporine; Tofacitinib; Deucravacitinib; Dupilumab; Tralokinumab; Guselkumab; Tildrakizumab; Baractinib; Abrocitinib; Upadacitinib; Lebrikizumab; Nemolizumab; Ruxolitinib; Bimekizumab; Roflumilast
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Not yet recruiting
- Start
- 2026-08-01
- Completion
- 2030-06-01
- Enrolment
- 10
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPsoriasis; Atopic DermatitisInterventionIn situ cutaneous microdevice; Triamcinolone; 5-Fluorouracil; Calcipotriene +32 morePhasePhase 4Registry statusNot yet recruitingThe Value of Methotrexate in NCES for Stable Vitiligo
NCT07352293 · start 2026-03-03
Registered record
- Registry ID
- NCT07352293
- Conditions
- Vitiligo
- Interventions
- Non cultured epidermal suspension
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Active not recruiting
- Start
- 2026-03-03
- Completion
- 2026-09
- Enrolment
- 20
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionVitiligoInterventionNon cultured epidermal suspensionPhasePhase 4Registry statusActive not recruitingA Study Using a Disease Registry to Observe the Long-term Effects of Nintedanib in People With Scleroderma-related Lung Fibrosis
NCT07080125 · start 2025-06-17
Registered record
- Registry ID
- NCT07080125
- Conditions
- Interstitial Lung Diseases; Systemic Sclerosis Associated Interstitial Lung Disease
- Interventions
- Ofev®
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Active not recruiting
- Start
- 2025-06-17
- Completion
- 2033-12-31
- Enrolment
- 2,000
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionInterstitial Lung Diseases; Systemic Sclerosis Associated Interstitial Lung DiseaseInterventionOfev®PhaseNot recordedRegistry statusActive not recruitingNewly-diagnosed Pediatric Ph-positive B-ALL Protocol
NCT07152041 · start 2025-03-28
Registered record
- Registry ID
- NCT07152041
- Conditions
- Acute Lymphoblastic Leukemia (ALL) Philadelphia Chromosome-positive (Ph+); Childhood Leukemia, Acute Lymphoblastic
- Interventions
- olverembatinib
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Recruiting
- Start
- 2025-03-28
- Completion
- 2030-06
- Enrolment
- 150
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAcute Lymphoblastic Leukemia (ALL) Philadelphia Chromosome-positive (Ph+); Childhood Leukemia, Acute LymphoblasticInterventionolverembatinibPhasePhase 3Registry statusRecruitingEffectiveness and Safety of InO±DLI for Relapsed B-ALL/LBL After Allo-HSCT
NCT06861348 · start 2025-03-01
Registered record
- Registry ID
- NCT06861348
- Conditions
- Leukemia, Lymphocytic, Acute
- Interventions
- Inotuzumab Ozogamicin±Donor Lymphocyte Infusion
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Not yet recruiting
- Start
- 2025-03-01
- Completion
- 2027-04-30
- Enrolment
- 23
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionLeukemia, Lymphocytic, AcuteInterventionInotuzumab Ozogamicin±Donor Lymphocyte InfusionPhasePhase 2Registry statusNot yet recruitingA Study of Dasatinib Plus Reduced Intensive Consolidation Chemotherapy in Ph+ Adult ALL
NCT05026229 · start 2021-09-06
Registered record
- Registry ID
- NCT05026229
- Conditions
- Precursor Cell Lymphoblastic Leukemia-Lymphoma; Philadelphia-Positive Acute Lymphoblastic Leukemia; ALL, Adult
- Interventions
- dasatinib plus consolidation chemotherapy with vincristine and prednisone; dasatinib plus consolidation chemotherapy with high-dose methotrexate and cytarabine
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Unknown
- Start
- 2021-09-06
- Completion
- 2023-06-30
- Enrolment
- 60
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPrecursor Cell Lymphoblastic Leukemia-Lymphoma; Philadelphia-Positive Acute Lymphoblastic Leukemia; ALL, AdultInterventiondasatinib plus consolidation chemotherapy with vincristine and prednisone; dasatinib plus consolidation chemotherapy with high-dose methotrexate and cytarabinePhaseNot applicableRegistry statusUnknownRL-MPV Followed by BBC HCT Using Autologous Stem Cells and Maintenance Therapy With Nivolumab for Newly Diagnosed PCNSL
NCT05425654 · start 2021-05-17
Registered record
- Registry ID
- NCT05425654
- Conditions
- Primary CNS Lymphoma
- Interventions
- Rituximab, Methotrexate, Vincristine, Procarbazine, Lenalidomide
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Unknown
- Start
- 2021-05-17
- Completion
- 2026-05
- Enrolment
- 30
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPrimary CNS LymphomaInterventionRituximab, Methotrexate, Vincristine, Procarbazine, LenalidomidePhasePhase 2Registry statusUnknownEffect of Two Methotrexate in Sync With the First Adalimumab to Prevent the Immunisation Anti Ada in Spondyloarthritis
NCT04360785 · start 2020-11-11
Registered record
- Registry ID
- NCT04360785
- Conditions
- Spondyloarthritis
- Interventions
- Methotrexate
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2020-11-11
- Completion
- 2023-02-27
- Enrolment
- 124
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSpondyloarthritisInterventionMethotrexatePhaseNot applicableRegistry statusCompletedMedical Treatment in Ectopic Tubal Pregnancy
NCT05208034 · start 2020-01-01
Registered record
- Registry ID
- NCT05208034
- Conditions
- Ectopic Pregnancy
- Interventions
- Methotrexate
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2020-01-01
- Completion
- 2021-07-30
- Enrolment
- 100
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionEctopic PregnancyInterventionMethotrexatePhaseNot applicableRegistry statusCompletedASP-1929 Photoimmunotherapy (PIT) Study in Recurrent Head/Neck Cancer for Patients Who Have Failed at Least Two Lines of Therapy
NCT03769506 · start 2019-05-09
Registered record
- Registry ID
- NCT03769506
- Conditions
- Head and Neck Cancer
- Interventions
- ASP-1929 Photoimmunotherapy; Physician's Choice SOC
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Active not recruiting
- Start
- 2019-05-09
- Completion
- 2025-12
- Enrolment
- 135
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHead and Neck CancerInterventionASP-1929 Photoimmunotherapy; Physician's Choice SOCPhasePhase 3Registry statusActive not recruitingSpanish Academy of Dermatology and Venereology Registry of Atopic Dermatitis Therapy
NCT05674695 · start 2019-01-01
Registered record
- Registry ID
- NCT05674695
- Conditions
- Dermatitis, Atopic
- Interventions
- Ciclosporin
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Recruiting
- Start
- 2019-01-01
- Completion
- 2029-01-01
- Enrolment
- 2,500
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionDermatitis, AtopicInterventionCiclosporinPhaseNot recordedRegistry statusRecruitingMulticentre ObservatioNal Initiative in Treat to Target Outcomes in Psoriatic Arthritis
NCT03531073 · start 2018-04-18
Registered record
- Registry ID
- NCT03531073
- Conditions
- Psoriatic Arthritis
- Interventions
- Methotrexate
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2018-04-18
- Completion
- 2024-12-31
- Enrolment
- 446
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPsoriatic ArthritisInterventionMethotrexatePhaseNot recordedRegistry statusCompletedEffect of Methotrexate on Inflammatory Response in Adult Atopic Dermatitis Patients
NCT03327116 · start 2017-11-01
Registered record
- Registry ID
- NCT03327116
- Conditions
- Atopic Dermatitis
- Interventions
- Methotrexate
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2017-11-01
- Completion
- 2018-12-01
- Enrolment
- 10
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAtopic DermatitisInterventionMethotrexatePhaseNot applicableRegistry statusCompletedA Study Comparing Upadacitinib (ABT-494) Monotherapy to Methotrexate (MTX) Monotherapy in Adults With Rheumatoid Arthritis (RA) Who Have an Inadequate Response to MTX (SELECT-MONOTHERAPY)
NCT02706951 · start 2016-03-23
Registered record
- Registry ID
- NCT02706951
- Conditions
- Rheumatoid Arthritis
- Interventions
- Methotrexate; Upadacitinib; Placebo Upadacitinib; Placebo Methotrexate
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2016-03-23
- Completion
- 2022-08-10
- Enrolment
- 648
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionRheumatoid ArthritisInterventionMethotrexate; Upadacitinib; Placebo Upadacitinib; Placebo MethotrexatePhasePhase 3Registry statusCompletedTransarterial Chemoperfusion: Cisplatin, Methotrexate, Gemcitabine for Unresectable Pleural Mesothelioma
NCT02611037 · start 2016-03-04
Registered record
- Registry ID
- NCT02611037
- Conditions
- Malignant Pleural Mesothelioma; Mesothelioma
- Interventions
- Cisplatin; Methotrexate; Gemcitabine; Lung Cancer Symptom Scale for Mesothelioma Questionnaire
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2016-03-04
- Completion
- 2024-01-26
- Enrolment
- 34
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMalignant Pleural Mesothelioma; MesotheliomaInterventionCisplatin; Methotrexate; Gemcitabine; Lung Cancer Symptom Scale for Mesothelioma QuestionnairePhasePhase 2Registry statusCompleted