Research dashboard
Search approved medicines for AI-predicted activity against four drug-resistant pathogens, and see what evidence is already documented for each one.
1,761
Approved medicines
Approved medicines matched to the FDA Orange Book, antimicrobials included
1,276
Medicines with ≥40% AI-predicted activity
Against at least one of the four supported pathogens; each medicine counted once
1,019
Repurposing candidates
Of those, the medicines that are not already antimicrobials
How the repurposing candidates are counted
1,761approved medicines
1,276with AI-predicted activity ≥40% against at least one pathogen
− 485 below ≥40%, not counted
1,120not already antimicrobials
− 156 already antimicrobials, set aside
1,019repurposing candidates
− 101 needing review, kept in the library
Existing antimicrobials are identified from WHO ATC codes and FDA pharmacologic classes. Medicines needing review (neither source says whether they are antimicrobials) stay in the approved-medicine download, marked “unclassified”. They are not assumed to be non-antimicrobials, so they are not counted as candidates.
Downloads
Download approved medicines (CSV)1,761 rowsDownload repurposing candidates (CSV)1,019 rowsPathogen coverage
A medicine can count under more than one
- MRSAMethicillin-resistant Staphylococcus aureus671Repurposing candidates with AI-predicted activity ≥40%860 at ≥40%:671 candidates117 antimicrobials72 needing reviewSee all 671 candidates →
- E. coliEscherichia coli336Repurposing candidates with AI-predicted activity ≥40%467 at ≥40%:336 candidates103 antimicrobials28 needing reviewSee all 336 candidates →
- K. pneumoniaeKlebsiella pneumoniae85Repurposing candidates with AI-predicted activity ≥40%199 at ≥40%:85 candidates98 antimicrobials16 needing reviewSee all 85 candidates →
- M. tuberculosisMycobacterium tuberculosis870Repurposing candidates with AI-predicted activity ≥40%1,072 at ≥40%:870 candidates128 antimicrobials74 needing reviewSee all 870 candidates →
Registered studies
A registration describes a study; it does not establish a positive result.
Gradual Tapering or Discontinuation of Beta-Blockers After Stabilization With Mavacamten Therapy
NCT07815301 · start 2026-12
Registered record
- Registry ID
- NCT07815301
- Conditions
- Obstructive Hypertrophic Cardiomyopathy (oHCM)
- Interventions
- Beta-Blocker Sequential Tapering and Discontinuation; Beta-Blocker Baseline Stable-Dose Maintenance
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Not yet recruiting
- Start
- 2026-12
- Completion
- 2028-12
- Enrolment
- 286
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionObstructive Hypertrophic Cardiomyopathy (oHCM)InterventionBeta-Blocker Sequential Tapering and Discontinuation; Beta-Blocker Baseline Stable-Dose MaintenancePhaseNot applicableRegistry statusNot yet recruitingModified FOLFIRINOX and Pentamidine in Advanced and Metastatic Pancreatic Cancer
NCT07829185 · start 2026-12
Registered record
- Registry ID
- NCT07829185
- Conditions
- Pancreatic Ductal Adenocarcinoma (PDAC)
- Interventions
- modified FOLFIRINOX; Pentamidine 300 MG Injection
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Not yet recruiting
- Start
- 2026-12
- Completion
- 2030-12
- Enrolment
- 30
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPancreatic Ductal Adenocarcinoma (PDAC)Interventionmodified FOLFIRINOX; Pentamidine 300 MG InjectionPhasePhase 1Registry statusNot yet recruitingEfficacy and Safety of Cryotherapy Followed by Tirbanibulin Ointment for Actinic Keratosis on the Scalp and Forehead
NCT07273656 · start 2026-11-30
Registered record
- Registry ID
- NCT07273656
- Conditions
- Keratosis; Actinic Keratoses
- Interventions
- Cryotherapy + Tirbanibulin
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Not yet recruiting
- Start
- 2026-11-30
- Completion
- 2028-11-30
- Enrolment
- 59
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionKeratosis; Actinic KeratosesInterventionCryotherapy + TirbanibulinPhasePhase 3Registry statusNot yet recruitingA Study of Lurbinectedin in Combination With Durvalumab for the Treatment of Participants With ES-SCLC
NCT07459634 · start 2026-11-30
Registered record
- Registry ID
- NCT07459634
- Conditions
- Extensive-stage Small-cell Lung Cancer
- Interventions
- Lurbinectedin; Durvalumab
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Recruiting
- Start
- 2026-11-30
- Completion
- 2028-04-30
- Enrolment
- 50
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionExtensive-stage Small-cell Lung CancerInterventionLurbinectedin; DurvalumabPhasePhase 2Registry statusRecruitingComparison of Serratus Posterior Superior Intercostal Plane Block and Deep Serratus Anterior Plane Block After Video-Assisted Thoracoscopic Surgery
NCT07553195 · start 2026-11-30
Registered record
- Registry ID
- NCT07553195
- Conditions
- Postoperative Pain; Video Assisted Thoracic Surgery (VATS); Serratus Posterior Superior Intercostal Plane Block; Deep Serratus Anterior Plane Block
- Interventions
- Serratus Posterior Superior Intercostal Plane (SPSIP) block; Deep Serratus Anterior Plane Block (Deep SAP)
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Not yet recruiting
- Start
- 2026-11-30
- Completion
- 2028-04-30
- Enrolment
- 60
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPostoperative Pain; Video Assisted Thoracic Surgery (VATS); Serratus Posterior Superior Intercostal Plane Block; Deep Serratus Anterior Plane BlockInterventionSerratus Posterior Superior Intercostal Plane (SPSIP) block; Deep Serratus Anterior Plane Block (Deep SAP)PhaseNot applicableRegistry statusNot yet recruitingEvaluation of 18F-Fluciclovine Positron Emission Tomography - Magnetic Resonance Imaging (PET-MRI) in LGG
NCT05555550 · start 2026-11-29
Registered record
- Registry ID
- NCT05555550
- Conditions
- Glioma; Low-grade Glioma; Low Grade Glioma of Brain; Glioma, Malignant; Glioma Intracranial
- Interventions
- 18F-Fluciclovine
- Study type
- INTERVENTIONAL
- Phase
- Early phase 1
- Registry status
- Recruiting
- Start
- 2026-11-29
- Completion
- 2028-09
- Enrolment
- 30
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionGlioma; Low-grade Glioma; Low Grade Glioma of Brain; Glioma, Malignant +1 moreIntervention18F-FluciclovinePhaseEarly phase 1Registry statusRecruitingTesting the Use of an IDH1 Inhibitor, Olutasidenib, in Acute Myeloid Leukemia Added to ASTX727 and Venetoclax; in High-Risk MDS Added to ASTX727; and Alone in Low Risk MDS (A MyeloMATCH Treatment Substudy)
NCT07153497 · start 2026-11-27
Registered record
- Registry ID
- NCT07153497
- Conditions
- Acute Myeloid Leukemia; Myelodysplastic Syndrome
- Interventions
- Biospecimen Collection; Bone Marrow Aspiration; Bone Marrow Biopsy; Decitabine and Cedazuridine; Olutasidenib; Venetoclax
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Not yet recruiting
- Start
- 2026-11-27
- Completion
- 2030-04-26
- Enrolment
- 132
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAcute Myeloid Leukemia; Myelodysplastic SyndromeInterventionBiospecimen Collection; Bone Marrow Aspiration; Bone Marrow Biopsy; Decitabine and Cedazuridine +2 morePhasePhase 2Registry statusNot yet recruitingA Study of Belzutifan in Adolescent Participants With Solid Tumors (MK-9999-01E/LIGHTBEAM-U01)
NCT07700758 · start 2026-11-23
Registered record
- Registry ID
- NCT07700758
- Conditions
- Malignant Neoplasm
- Interventions
- Belzutifan
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Not yet recruiting
- Start
- 2026-11-23
- Completion
- 2034-01-02
- Enrolment
- 15
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMalignant NeoplasmInterventionBelzutifanPhasePhase 2Registry statusNot yet recruitingA Study to Learn About the Safety of Diroximel Fumarate (DRF) and Dimethyl Fumarate (DMF) and Their Effects on Relapses in Pediatric Participants With Relapsing Forms of Multiple Sclerosis (RMS)
NCT07483632 · start 2026-11-16
Registered record
- Registry ID
- NCT07483632
- Conditions
- Relapsing Forms of Multiple Sclerosis
- Interventions
- Diroximel Fumarate; Dimethyl Fumarate; Fingolimod; Placebo matching DRF; Placebo matching DMF; Placebo matching fingolimod
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Not yet recruiting
- Start
- 2026-11-16
- Completion
- 2035-06-19
- Enrolment
- 185
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionRelapsing Forms of Multiple SclerosisInterventionDiroximel Fumarate; Dimethyl Fumarate; Fingolimod; Placebo matching DRF +2 morePhasePhase 3Registry statusNot yet recruitingMinoxidil 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 recruitingEffect of Theravex Tissue Care on Implant Stability
NCT07707388 · start 2026-11-12
Registered record
- Registry ID
- NCT07707388
- Conditions
- Immediate Dental Implant Placement
- Interventions
- Bone Bioactive Liquid; Bovine-derived Xenograft; Immediate Implant Placement
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Not yet recruiting
- Start
- 2026-11-12
- Completion
- 2027-09-08
- Enrolment
- 30
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionImmediate Dental Implant PlacementInterventionBone Bioactive Liquid; Bovine-derived Xenograft; Immediate Implant PlacementPhaseNot applicableRegistry statusNot yet recruitingEfficacy and Safety of Emodepside in Participants With Soil-transmitted Helminth Infections
NCT06800248 · start 2026-11-06
Registered record
- Registry ID
- NCT06800248
- Conditions
- Trichuris Trichiura; Infection; Hookworm Infection; Ascaris Lumbricoides Infection
- Interventions
- emodepside (BAY 44-4400); Mebendazole 100 MG; similar placebo to mebendazole; matching placebo of emodepside
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Not yet recruiting
- Start
- 2026-11-06
- Completion
- 2027-10
- Enrolment
- 315
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionTrichuris Trichiura; Infection; Hookworm Infection; Ascaris Lumbricoides InfectionInterventionemodepside (BAY 44-4400); Mebendazole 100 MG; similar placebo to mebendazole; matching placebo of emodepsidePhasePhase 3Registry statusNot yet recruitingDigital Treatment for Chronic Pain and Addiction in Veterans With Opioid Use Disorder Receiving Buprenorphine
NCT07361432 · start 2026-11-02
Registered record
- Registry ID
- NCT07361432
- Conditions
- Opioid Use Disorder; Chronic Pain
- Interventions
- Integrating the Management of Pain and Addiction via Collaborative Treatment (IMPACT); Enhanced Treatment as Usual (ETAU)
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Not yet recruiting
- Start
- 2026-11-02
- Completion
- 2030-05-31
- Enrolment
- 250
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionOpioid Use Disorder; Chronic PainInterventionIntegrating the Management of Pain and Addiction via Collaborative Treatment (IMPACT); Enhanced Treatment as Usual (ETAU)PhasePhase 3Registry statusNot yet recruitingSafety, Tolerability, and Efficacy of PLX-200 in Patients With CLN3
NCT04637282 · start 2026-11-01
Registered record
- Registry ID
- NCT04637282
- Conditions
- Juvenile Neuronal Ceroid Lipofuscinosis
- Interventions
- PLX-200; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Withdrawn
- Start
- 2026-11-01
- Completion
- 2026-12-31
- Enrolment
- 0
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionJuvenile Neuronal Ceroid LipofuscinosisInterventionPLX-200; PlaceboPhasePhase 3Registry statusWithdrawnEfficacy of Essential Phospholipid Versus Betaine HCL/L-Glutamic Acid in MAFLD
NCT07194863 · start 2026-11-01
Registered record
- Registry ID
- NCT07194863
- Conditions
- Essential Phospholipid in Metabolic Associated Fatty Liver Disease
- Interventions
- Not recorded
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Not yet recruiting
- Start
- 2026-11-01
- Completion
- 2027-09-01
- Enrolment
- 200
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionEssential Phospholipid in Metabolic Associated Fatty Liver DiseaseInterventionNot recordedPhaseNot recordedRegistry statusNot yet recruiting
AI-predicted activity is a model’s estimate that a molecule is active against a pathogen in the laboratory. It is not clinical effectiveness. The models describe each pathogen species; the data behind them rarely records resistant strains.