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.
- Galantamine HydrobromideExisting use: Alzheimer disease, Dementia89.6% AI-predicted activityagainst K. pneumoniaeLab records exist50+ registered studies
- Chlorhexidine GluconateExisting use: Eye infection, Gingivitis, Infection and 2 more69.3% AI-predicted activityagainst K. pneumoniaeLab records exist50+ registered studies
- TriclosanExisting use: Phenol and derivatives, Medicated dressings with antiinfectives68.0% AI-predicted activityagainst K. pneumoniaeLab records exist50+ registered studies
- ElvitegravirExisting use: HIV infection, HIV-1 infection, Viral disease60.2% AI-predicted activityagainst K. pneumoniae50+ registered studies
- Caspofungin AcetateExisting use: Aspergillosis, Candidemia, Candidiasis and 1 more57.5% AI-predicted activityagainst K. pneumoniae50+ registered studies
- DactinomycinExisting use: Kidney Wilms tumor, Neoplasm56.8% AI-predicted activityagainst K. pneumoniae50+ registered studies
- CyclosporineExisting use: Conjunctivitis, Corneal disease, Eye disease and 6 more56.1% AI-predicted activityagainst K. pneumoniae50+ registered studies
- LinaclotideExisting use: Constipation, Constipation disorder, Irritable bowel syndrome56.0% AI-predicted activityagainst K. pneumoniae50+ registered studies
- Irinotecan HydrochlorideExisting use: Adenocarcinoma, Cancer, Carcinoma and 4 more54.5% AI-predicted activityagainst K. pneumoniae50+ registered studies
- OxytocinExisting use: Hemorrhage, Uterine Inertia52.7% AI-predicted activityagainst K. pneumoniae50+ registered studies
- Micafungin SodiumExisting use: Candidiasis52.4% AI-predicted activityagainst K. pneumoniae50+ registered studies
- VoclosporinExisting use: Immune system disease, Lupus nephritis52.2% AI-predicted activityagainst K. pneumoniae28 registered studies
Registered studies
A registration describes a study; it does not establish a positive result.
PET/MR Imaging In Patients With Cardiac Sarcoidosis
NCT03705884 · start 2017-10-30
Registered record
- Registry ID
- NCT03705884
- Conditions
- Cardiac Sarcoidosis
- Interventions
- 18F-FDG; Prednisolone
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2017-10-30
- Completion
- 2018-12-01
- Enrolment
- 40
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCardiac SarcoidosisIntervention18F-FDG; PrednisolonePhaseNot applicableRegistry statusCompletedNon-alcoholic Fatty Liver Disease Parametric PET (FLiPP) Study
NCT02754037 · start 2016-04-30
Registered record
- Registry ID
- NCT02754037
- Conditions
- Non-alcoholic Fatty Liver Disease (NAFLD); Non-alcoholic Steatohepatitis (NASH)
- Interventions
- Fluorodeoxyglucose (FDG) positron emission tomography (PET); Magnetic resonance imaging (MRI); PET Explorer
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Active not recruiting
- Start
- 2016-04-30
- Completion
- 2026-06-30
- Enrolment
- 120
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionNon-alcoholic Fatty Liver Disease (NAFLD); Non-alcoholic Steatohepatitis (NASH)InterventionFluorodeoxyglucose (FDG) positron emission tomography (PET); Magnetic resonance imaging (MRI); PET ExplorerPhaseNot recordedRegistry statusActive not recruitingPET Combined With MRI for Monitoring Inflammatory Activity in Patients With Ulcerative Colitis
NCT03781284 · start 2016-01-01
Registered record
- Registry ID
- NCT03781284
- Conditions
- Ulcerative Colitis
- Interventions
- [18F]-FDG PET/MRI; Colonoscopy
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2016-01-01
- Completion
- 2018-10-31
- Enrolment
- 53
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionUlcerative ColitisIntervention[18F]-FDG PET/MRI; ColonoscopyPhaseNot applicableRegistry statusCompletedUse of PET/MR Imaging in Chronic Pain
NCT03195270 · start 2014-11-24
Registered record
- Registry ID
- NCT03195270
- Conditions
- Chronic Pain
- Interventions
- [18F]FDG; PET/MRI
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2014-11-24
- Completion
- 2022-01-20
- Enrolment
- 88
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionChronic PainIntervention[18F]FDG; PET/MRIPhasePhase 1Registry statusCompletedIntestinal Remodeling And Reprogramming of Glucose Metabolism Following Laparoscopic Roux-en-Y Gastric Bypass
NCT02288351 · start 2014-11
Registered record
- Registry ID
- NCT02288351
- Conditions
- Type 2 Diabetes; Obesity
- Interventions
- Mix Nutrient Meal; labs; Biopsy; Second Mix Nutrient Meal; Second biopsy; PET/CT
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Withdrawn
- Start
- 2014-11
- Completion
- 2015-04
- Enrolment
- 0
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionType 2 Diabetes; ObesityInterventionMix Nutrient Meal; labs; Biopsy; Second Mix Nutrient Meal +2 morePhaseNot applicableRegistry statusWithdrawn68Ga-AlfatideII for the Differential Diagnosis of of Lung Cancer and Lung Tuberculosis by PET/CT
NCT02481726 · start 2014-03
Registered record
- Registry ID
- NCT02481726
- Conditions
- Lung Cancer; Lung Tuberculosis
- Interventions
- 68Ga-labeled peptides of dimer RGD (Alfatide II) and 18F-FDG
- Study type
- INTERVENTIONAL
- Phase
- Phase 1 / Phase 2
- Registry status
- Completed
- Start
- 2014-03
- Completion
- Not recorded
- Enrolment
- 31
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionLung Cancer; Lung TuberculosisIntervention68Ga-labeled peptides of dimer RGD (Alfatide II) and 18F-FDGPhasePhase 1 / Phase 2Registry statusCompletedEarly Interim 18F-FDG-PET and 18F-FLT-PET for Predicting Treatment Response and Survival in Metastatic Breast Cancer
NCT04411966 · start 2014-01-01
Registered record
- Registry ID
- NCT04411966
- Conditions
- Metastatic Breast Cancer
- Interventions
- 18F-fluorothymidine
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2014-01-01
- Completion
- 2019-05-30
- Enrolment
- 32
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMetastatic Breast CancerIntervention18F-fluorothymidinePhaseNot applicableRegistry statusCompletedFunctional Brain Imaging in PTSD
NCT02053532 · start 2013-05
Registered record
- Registry ID
- NCT02053532
- Conditions
- Post-traumatic Stress Disorder (PTSD); Trauma
- Interventions
- Positron emission tomography/magnetic resonance imaging
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2013-05
- Completion
- 2016-02
- Enrolment
- 50
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPost-traumatic Stress Disorder (PTSD); TraumaInterventionPositron emission tomography/magnetic resonance imagingPhaseNot recordedRegistry statusCompletedPerformance of PET 18 F-FDG Coupled to CT With Contrast Injection Iodized in the Diagnosis of Early Recurrences of Head and Neck Carcinoma Treated With Concurrent Chemoradiation. Comparison With 18F-FDG PET Coupled With CT Not Injected With Filling CT Standard Injection
NCT02510872 · start 2011-12
Registered record
- Registry ID
- NCT02510872
- Conditions
- Squamous Cell Carcinoma of the Head and Neck
- Interventions
- 18F-FDG PET combined with CT with iodinated contrast injection; 18F-FDG PET combined with CT without injection
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2011-12
- Completion
- Not recorded
- Enrolment
- 19
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSquamous Cell Carcinoma of the Head and NeckIntervention18F-FDG PET combined with CT with iodinated contrast injection; 18F-FDG PET combined with CT without injectionPhaseNot applicableRegistry statusCompletedPredictive Value of FDG PET/CT, DWI and DCE-MRI Scans for Non-small Cell Lung Cancer Patients Receiving Chemotherapy
NCT01482182 · start 2011-11
Registered record
- Registry ID
- NCT01482182
- Conditions
- Non-small Cell Lung Cancer
- Interventions
- Not recorded
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2011-11
- Completion
- 2014-01
- Enrolment
- 35
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionNon-small Cell Lung CancerInterventionNot recordedPhaseNot recordedRegistry statusCompletedMRI and PET-CT for Radiotherapy Planning for Head and Neck Cancer
NCT02273778 · start 2011-06
Registered record
- Registry ID
- NCT02273778
- Conditions
- Head and Neck Cancer
- Interventions
- MRI Scan; PET-CT Scan; No intervention
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2011-06
- Completion
- 2013-06
- Enrolment
- Not recorded
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHead and Neck CancerInterventionMRI Scan; PET-CT Scan; No interventionPhaseNot applicableRegistry statusCompletedCediranib, Temozolomide, and Radiation Therapy in Treating Patients With Newly Diagnosed Glioblastoma
NCT00662506 · start 2008-04
Registered record
- Registry ID
- NCT00662506
- Conditions
- Adult Giant Cell Glioblastoma; Adult Glioblastoma; Adult Gliosarcoma
- Interventions
- Cediranib Maleate; Diffusion Tensor Imaging; Diffusion Weighted Imaging; Dynamic Contrast-Enhanced Magnetic Resonance Imaging; Fludeoxyglucose F-18; Intensity-Modulated Radiation Therapy; Laboratory Biomarker Analysis; Perfusion Magnetic Resonance Imaging; Positron Emission Tomography; Temozolomide
- Study type
- INTERVENTIONAL
- Phase
- Phase 1 / Phase 2
- Registry status
- Completed
- Start
- 2008-04
- Completion
- 2014-04
- Enrolment
- 46
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAdult Giant Cell Glioblastoma; Adult Glioblastoma; Adult GliosarcomaInterventionCediranib Maleate; Diffusion Tensor Imaging; Diffusion Weighted Imaging; Dynamic Contrast-Enhanced Magnetic Resonance Imaging +6 morePhasePhase 1 / Phase 2Registry statusCompletedObservation Study for Prediction of Allograft Survival and Impact of Imaging in Kidney Transplant Recipients.
NCT03764124 · start 2007-01-01
Registered record
- Registry ID
- NCT03764124
- Conditions
- Kidney Transplantation
- Interventions
- PET/CT imaging
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Unknown
- Start
- 2007-01-01
- Completion
- 2024-08
- Enrolment
- 1,000
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionKidney TransplantationInterventionPET/CT imagingPhaseNot recordedRegistry statusUnknownFluorodeoxyglucose (FDG)-Positron Emission Tomography (PET) in Cancer Associated Venothromboembolism
NCT01107327 · start 2006-08
Registered record
- Registry ID
- NCT01107327
- Conditions
- Venothromboembolism
- Interventions
- FDG-PET/CT
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2006-08
- Completion
- 2012-01
- Enrolment
- 26
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionVenothromboembolismInterventionFDG-PET/CTPhaseNot recordedRegistry statusCompletedWhole-Body 18F-FDG PET in Induction Chemotherapeutic Response for Advanced NPC Patients
NCT00304694 · start 2006-03
Registered record
- Registry ID
- NCT00304694
- Conditions
- Nasopharyngeal Cancer
- Interventions
- Not recorded
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Unknown
- Start
- 2006-03
- Completion
- Not recorded
- Enrolment
- 50
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionNasopharyngeal CancerInterventionNot recordedPhaseNot recordedRegistry statusUnknown