Fludeoxyglucose F-18
FDA-approved product (injectable, injection), marketed as Fludeoxyglucose F18.
- Registered studies
- 50+
- Lab records
- 0
- Pathogens at ≥40%
- 0 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLNo approved indication recorded
ChEMBL records no approved indication for Fludeoxyglucose F-18. Its therapeutic class is shown instead.
- WHO therapeutic group
- Other diagnostic radiopharmaceuticals for tumour detection
- FDA pharmacologic class
- Radioactive Diagnostic Agent FDA label ↗
- Anti-infective classification
- Not classified as an anti-infective.
Repurposing investigation
No supported pathogen reaches ≥40% AI-predicted activity for Fludeoxyglucose F-18, so it is not among the repurposing candidates. Its predictions are shown below.
AI-predicted activity
AI prediction · nothing measured- MRSA18.1% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- E. coli6.3% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- K. pneumoniae21.3% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- M. tuberculosis13.9% 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
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 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 Fludeoxyglucose F-18 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.
- FurazolidoneExisting use: Other antiinfectives and antiseptics91.4% AI-predicted activityagainst M. tuberculosisLab records exist49 registered studies
- TriflupromazineExisting use: Psychosis90.6% AI-predicted activityagainst M. tuberculosisNo documented evidence found
- ValdecoxibExisting use: Dysmenorrhea, Osteoarthritis, Rheumatic disease and 1 more88.6% AI-predicted activityagainst M. tuberculosisLab records exist31 registered studies
- CelecoxibExisting use: Ankylosing spondylitis, Cancer, Colorectal neoplasm and 15 more87.6% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
- Dorzolamide HydrochlorideExisting use: Glaucoma, Ocular hypertension, Open-angle glaucoma86.8% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
- MethazolamideExisting use: Glaucoma, Open-angle glaucoma85.6% AI-predicted activityagainst M. tuberculosisLab records exist11 registered studies
- AcetazolamideExisting use: Altitude sickness, Angle-closure glaucoma, Congestive heart failure and 5 more85.2% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
- Trifluoperazine HydrochlorideExisting use: Anxiety disorder, Mental or behavioural disorder, Psychosis and 1 more84.6% AI-predicted activityagainst M. tuberculosis1 registered study
- TriclosanExisting use: Phenol and derivatives, Medicated dressings with antiinfectives84.2% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
- NitrofurazoneExisting use: Eye infection, Leishmaniasis, Trypanosomiasis84.0% AI-predicted activityagainst M. tuberculosis8 registered studies
- BrinzolamideExisting use: Glaucoma, Ocular hypertension, Open-angle glaucoma83.8% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
- ZonisamideExisting use: Epilepsy, Focal-onset seizure, Partial epilepsy and 1 more82.8% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
Registered studies
A registration describes a study; it does not establish a positive result.
(89Zr Panitumumab) With PET/CT for Diagnosing Metastases in Patients With Head and Neck Squamous Cell Carcinoma
NCT05747625 · start 2023-05-09
Registered record
- Registry ID
- NCT05747625
- Conditions
- Head and Neck Squamous Cell Carcinoma; Metastatic Head and Neck Squamous Cell Carcinoma; Stage IV Cutaneous Squamous Cell Carcinoma of the Head and Neck
- Interventions
- Panitumumab; Zirconium Zr 89 Panitumumab; Positron Emission Tomography; Computed Tomography; Electronic Health Record Review
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Recruiting
- Start
- 2023-05-09
- Completion
- 2030-03-01
- Enrolment
- 60
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHead and Neck Squamous Cell Carcinoma; Metastatic Head and Neck Squamous Cell Carcinoma; Stage IV Cutaneous Squamous Cell Carcinoma of the Head and NeckInterventionPanitumumab; Zirconium Zr 89 Panitumumab; Positron Emission Tomography; Computed Tomography +1 morePhasePhase 1Registry statusRecruitingCharacterization of priMary And sEcondary STress Related takOtsubo
NCT05793008 · start 2023-03-30
Registered record
- Registry ID
- NCT05793008
- Conditions
- Takotsubo Cardiomyopathy; Sepsis-induced Cardiomyopathy
- Interventions
- Positron Emission Tomography (PET) analysis; Blood samples collection; Clinical follow up visit
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Unknown
- Start
- 2023-03-30
- Completion
- 2026-09-02
- Enrolment
- 60
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionTakotsubo Cardiomyopathy; Sepsis-induced CardiomyopathyInterventionPositron Emission Tomography (PET) analysis; Blood samples collection; Clinical follow up visitPhaseNot applicableRegistry statusUnknownActivation of Brown Adipose Tissue Thermogenesis in Humans Using Formoterol Fumarate (GB10)
NCT05553184 · start 2022-07-05
Registered record
- Registry ID
- NCT05553184
- Conditions
- Type 2 Diabetes; Obesity
- Interventions
- Formoterol Fumarate 12 micrograms Inhalation Powder; Nicotinic Acid 50 MG Oral Tablet; Acute Cold Exposure; Positron Emission Tomography (PET); Indirect calorimetry; dual-energy x-ray absorptiometry (DEXA scan); Biopsy; iv lines; Electromyogram (EMG)
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2022-07-05
- Completion
- 2023-05-29
- Enrolment
- 12
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionType 2 Diabetes; ObesityInterventionFormoterol Fumarate 12 micrograms Inhalation Powder; Nicotinic Acid 50 MG Oral Tablet; Acute Cold Exposure; Positron Emission Tomography (PET) +5 morePhaseNot applicableRegistry statusCompletedA Head-to-head Comparative Study of 18F-PSMA-1007 PET/CT and 18F-FDG PET/CT Imaging in Multiple Myeloma
NCT05448404 · start 2022-03-08
Registered record
- Registry ID
- NCT05448404
- Conditions
- Multiple Myeloma
- Interventions
- 18F-PSMA-1007; 18F-FDG
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Unknown
- Start
- 2022-03-08
- Completion
- 2023-06-30
- Enrolment
- 30
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMultiple MyelomaIntervention18F-PSMA-1007; 18F-FDGPhaseNot applicableRegistry statusUnknownUsefulness of 18F-FDG PET/CT in the Initial Staging and Surveillance of Endometrial Cancer Patients
NCT05056259 · start 2022-01-01
Registered record
- Registry ID
- NCT05056259
- Conditions
- Endometrial Cancer
- Interventions
- 18F-FDG PET/CT
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Unknown
- Start
- 2022-01-01
- Completion
- 2023-10
- Enrolment
- 42
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionEndometrial CancerIntervention18F-FDG PET/CTPhaseNot recordedRegistry statusUnknownPET Imaging of Systemic Sclerosis Using FDG and 68Ga-DOTA-Siglec-9
NCT05108857 · start 2021-11-29
Registered record
- Registry ID
- NCT05108857
- Conditions
- Systemic Sclerosis
- Interventions
- Not recorded
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Enrolling by invitation
- Start
- 2021-11-29
- Completion
- 2026-12-31
- Enrolment
- 10
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSystemic SclerosisInterventionNot recordedPhaseNot recordedRegistry statusEnrolling by invitationPET-imaging of Unruptured Intracranial Aneurysm Inflammation
NCT04715503 · start 2021-01-14
Registered record
- Registry ID
- NCT04715503
- Conditions
- Intracranial Aneurysm; Cerebral Aneurysm; Inflammation
- Interventions
- PET imaging, 18F-FDG; PET imaging, 68Ga-DOTANOC
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Unknown
- Start
- 2021-01-14
- Completion
- 2022-10
- Enrolment
- 20
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionIntracranial Aneurysm; Cerebral Aneurysm; InflammationInterventionPET imaging, 18F-FDG; PET imaging, 68Ga-DOTANOCPhaseNot applicableRegistry statusUnknownCombined [18F]-FDG PET-MRI in Diagnostics and Surveillance of Small Bowel Crohn's Disease
NCT06796959 · start 2020-08-01
Registered record
- Registry ID
- NCT06796959
- Conditions
- Small Bowel Crohn' s Disease
- Interventions
- Not recorded
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2020-08-01
- Completion
- 2024-10-31
- Enrolment
- 35
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSmall Bowel Crohn' s DiseaseInterventionNot recordedPhaseNot recordedRegistry statusCompletedStudy for Quantitative Analysis of the Recovered COVID-19 Patients by 18F-FDG-PET/CT
NCT04519255 · start 2020-07-01
Registered record
- Registry ID
- NCT04519255
- Conditions
- PET/CT; COVID-19; Respiratory Function; Inflammatory Lesions
- Interventions
- Not recorded
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Unknown
- Start
- 2020-07-01
- Completion
- 2023-07-31
- Enrolment
- 60
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPET/CT; COVID-19; Respiratory Function; Inflammatory LesionsInterventionNot recordedPhaseNot recordedRegistry statusUnknownMarkers to Evaluate the Efficacy of PH-based Regimen as a Neoadjuvant Therapy for Operable HER2 Positive Breast Cancer
NCT04281641 · start 2020-04-21
Registered record
- Registry ID
- NCT04281641
- Conditions
- HER2-positive Breast Cancer
- Interventions
- TCHP
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Recruiting
- Start
- 2020-04-21
- Completion
- 2030-04-30
- Enrolment
- 94
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHER2-positive Breast CancerInterventionTCHPPhaseNot applicableRegistry statusRecruitingLower-Dose Chemoradiation in Treating Patients With Early-Stage Anal Cancer, the DECREASE Study
NCT04166318 · start 2020-01-02
Registered record
- Registry ID
- NCT04166318
- Conditions
- Anal Basaloid Carcinoma; Anal Canal Cloacogenic Carcinoma; Anal Canal Squamous Cell Carcinoma; Anal Margin Squamous Cell Carcinoma; Stage I Anal Cancer AJCC v8; Stage IIA Anal Cancer AJCC v8
- Interventions
- Biopsy; Biospecimen Collection; Capecitabine; Computed Tomography; Fludeoxyglucose F-18; Fluorouracil; Intensity-Modulated Radiation Therapy; Magnetic Resonance Imaging; Mitomycin; Positron Emission Tomography; Quality-of-Life Assessment; Questionnaire Administration
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Active not recruiting
- Start
- 2020-01-02
- Completion
- 2029-12-31
- Enrolment
- 252
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAnal Basaloid Carcinoma; Anal Canal Cloacogenic Carcinoma; Anal Canal Squamous Cell Carcinoma; Anal Margin Squamous Cell Carcinoma +2 moreInterventionBiopsy; Biospecimen Collection; Capecitabine; Computed Tomography +8 morePhasePhase 2Registry statusActive not recruitingDe-intensified Radiation Therapy With Chemotherapy (Cisplatin) or Immunotherapy (Nivolumab) in Treating Patients With Early-Stage, HPV-Positive, Non-Smoking Associated Oropharyngeal Cancer
NCT03952585 · start 2019-10-09
Registered record
- Registry ID
- NCT03952585
- Conditions
- Basaloid Squamous Cell Carcinoma; Clinical Stage I HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8; Clinical Stage II HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8; Oropharyngeal Squamous Cell Carcinoma; Papillary Squamous Cell Carcinoma; Pathologic Stage I HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8; Pathologic Stage II HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8; Squamous Cell Carcinoma
- Interventions
- Biopsy Procedure; Biospecimen Collection; Cisplatin; Computed Tomography; Fludeoxyglucose F-18; Image Guided Radiation Therapy; Intensity-Modulated Radiation Therapy; Magnetic Resonance Imaging; Nivolumab; Positron Emission Tomography; Quality-of-Life Assessment; Questionnaire Administration
- Study type
- INTERVENTIONAL
- Phase
- Phase 2 / Phase 3
- Registry status
- Active not recruiting
- Start
- 2019-10-09
- Completion
- 2026-12-11
- Enrolment
- 384
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionBasaloid Squamous Cell Carcinoma; Clinical Stage I HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8; Clinical Stage II HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8; Oropharyngeal Squamous Cell Carcinoma +4 moreInterventionBiopsy Procedure; Biospecimen Collection; Cisplatin; Computed Tomography +8 morePhasePhase 2 / Phase 3Registry statusActive not recruitingF-18 FDG- PETCT in Staging and Recurrent Colorectal Cancer
NCT03572595 · start 2018-07-01
Registered record
- Registry ID
- NCT03572595
- Conditions
- Colo-rectal Cancer; Recurrence
- Interventions
- F-18 FDG-PET/CT
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Unknown
- Start
- 2018-07-01
- Completion
- 2020-02-01
- Enrolment
- 45
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionColo-rectal Cancer; RecurrenceInterventionF-18 FDG-PET/CTPhaseNot recordedRegistry statusUnknownEvaluation of a Metabolic Preparation by a Low-carbohydrate Diet as Atkins-diet to Help in Detecting Infective Endocarditis by 18F-FDG PET
NCT03465098 · start 2018-03-19
Registered record
- Registry ID
- NCT03465098
- Conditions
- Infective Endocarditis
- Interventions
- Strict low carbohydrate diet (< 3gr/day of carbohydrate) before a 18F-FDG PET/CT
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2018-03-19
- Completion
- 2021-08-03
- Enrolment
- 26
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionInfective EndocarditisInterventionStrict low carbohydrate diet (< 3gr/day of carbohydrate) before a 18F-FDG PET/CTPhaseNot applicableRegistry statusCompletedPPG Project 3 - PET/MRI of the Brain-hematopoiesis-atherosclerosis Axis in PTSD Patients
NCT03279393 · start 2017-11-28
Registered record
- Registry ID
- NCT03279393
- Conditions
- PTSD; Trauma; Healthy
- Interventions
- fluorodeoxyglucose (FDG)-PET/MRI
- Study type
- INTERVENTIONAL
- Phase
- Early phase 1
- Registry status
- Completed
- Start
- 2017-11-28
- Completion
- 2023-02-14
- Enrolment
- 190
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPTSD; Trauma; HealthyInterventionfluorodeoxyglucose (FDG)-PET/MRIPhaseEarly phase 1Registry statusCompleted