Regadenoson
FDA-approved product (solution, intravenous), marketed as Lexiscan, Regadenoson.
- Registered studies
- 50+
- Lab records
- 0
- Pathogens at ≥40%
- 2 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Cardiovascular disease
- Myocardial Perfusion Imaging
Indications ChEMBL records as approved, from FDA and DailyMed labels.
- WHO therapeutic group
- Other cardiac preparations
- FDA pharmacologic class
- Adenosine Receptor Agonist 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 and E. coli. It was surfaced computationally for further investigation; it is not an established treatment for these infections.
AI-predicted activity
AI prediction · nothing measured- MRSA35.3% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- E. coli48.4% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- K. pneumoniae23.8% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- M. tuberculosis48.1% 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
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 Regadenoson 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.
Technical Development of Cardiovascular Magnetic Resonance Imaging (CMR) Using a Low Specific Absorption Rate (SAR) Scanner System
NCT03331380 · start 2018-01-05
Registered record
- Registry ID
- NCT03331380
- Conditions
- CAD
- Interventions
- MRI scan - obj 1; MRI scans - obj 2; MRI scans - obj 3; MRI scans - obj 4
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Recruiting
- Start
- 2018-01-05
- Completion
- 2028-05-31
- Enrolment
- 2,950
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCADInterventionMRI scan - obj 1; MRI scans - obj 2; MRI scans - obj 3; MRI scans - obj 4PhaseNot applicableRegistry statusRecruitingDetermining the Mechanism of Myocardial Injury and Role of Coronary Disease in Type 2 Myocardial Infarction
NCT03338504 · start 2017-10-23
Registered record
- Registry ID
- NCT03338504
- Conditions
- Myocardial Infarction, Acute; Myocardial Ischemia; Myocardial Injury
- Interventions
- Invasive coronary angiography; CT coronary angiography; Cardiac MRI
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2017-10-23
- Completion
- 2021-11-06
- Enrolment
- 100
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMyocardial Infarction, Acute; Myocardial Ischemia; Myocardial InjuryInterventionInvasive coronary angiography; CT coronary angiography; Cardiac MRIPhaseNot recordedRegistry statusCompletedA Dose Titration Study to Assess the Effects of SAR407899 in Patients With MVA and/or Persistent Stable Angina Despite Angiographically Successful PCI
NCT03236311 · start 2017-10-12
Registered record
- Registry ID
- NCT03236311
- Conditions
- Microvascular Coronary Artery Disease
- Interventions
- SAR407899; Placebo; Adenosine; Regadenoson; 13N-ammonia; 82Rubidium
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Terminated
- Start
- 2017-10-12
- Completion
- 2018-07-23
- Enrolment
- 10
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMicrovascular Coronary Artery DiseaseInterventionSAR407899; Placebo; Adenosine; Regadenoson +2 morePhasePhase 2Registry statusTerminatedQuantitative 13N-Ammonia Cardiac Rest/Stress Digital PET/CT
NCT03170817 · start 2017-03-29
Registered record
- Registry ID
- NCT03170817
- Conditions
- Coronary Artery Disease
- Interventions
- Cardiac Perfusion Rest/Stress Digital PET/CT; N-13 ammonia; Regadenoson
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2017-03-29
- Completion
- 2021-09-01
- Enrolment
- 15
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCoronary Artery DiseaseInterventionCardiac Perfusion Rest/Stress Digital PET/CT; N-13 ammonia; RegadenosonPhaseNot recordedRegistry statusCompletedUtility of Regadenoson Low-dose Dynamic Computed Tomography for Myocardial Perfusion Assesment (ULYSSES Study).
NCT03917199 · start 2016-11
Registered record
- Registry ID
- NCT03917199
- Conditions
- Myocardial Perfusion Imaging; Computed Tomography; Coronary Artery Disease
- Interventions
- Not recorded
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2016-11
- Completion
- 2019-07-11
- Enrolment
- 60
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMyocardial Perfusion Imaging; Computed Tomography; Coronary Artery DiseaseInterventionNot recordedPhaseNot recordedRegistry statusCompletedSimultaneous Assessment of FFR and SPECT
NCT02749045 · start 2016-07
Registered record
- Registry ID
- NCT02749045
- Conditions
- Coronary Artery Disease
- Interventions
- SPECT imaging
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Terminated
- Start
- 2016-07
- Completion
- 2021-06
- Enrolment
- 27
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCoronary Artery DiseaseInterventionSPECT imagingPhaseNot applicableRegistry statusTerminatedPerfusion Imaging With Myocardial Contrast Echocardiography in HCM
NCT02560467 · start 2015-12-01
Registered record
- Registry ID
- NCT02560467
- Conditions
- Hypertrophic Cardiomyopathy
- Interventions
- Echo and myocardial contrast echocardiography perfusion imaging
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Unknown
- Start
- 2015-12-01
- Completion
- 2019-09-15
- Enrolment
- 10
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHypertrophic CardiomyopathyInterventionEcho and myocardial contrast echocardiography perfusion imagingPhaseNot applicableRegistry statusUnknownAccuracy of an Echo-Stress Protocol Using Regadenoson With Speckle Tracking
NCT02130453 · start 2014-09-30
Registered record
- Registry ID
- NCT02130453
- Conditions
- Ischemia
- Interventions
- Regadenoson
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2014-09-30
- Completion
- 2024-06-28
- Enrolment
- 161
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionIschemiaInterventionRegadenosonPhasePhase 4Registry statusCompletedRegadenoson for Acute Vasoreactivity Testing in Pulmonary Hypertension
NCT02220634 · start 2014-08
Registered record
- Registry ID
- NCT02220634
- Conditions
- Pulmonary Hypertension
- Interventions
- Regadenoson
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Terminated
- Start
- 2014-08
- Completion
- 2017-05-25
- Enrolment
- 10
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPulmonary HypertensionInterventionRegadenosonPhaseNot applicableRegistry statusTerminatedArtifact-Free High-Resolution Myocardial Perfusion MRI in Subjects With Abnormal Nuclear Myocardial Perfusion Studies
NCT01949844 · start 2014-05-16
Registered record
- Registry ID
- NCT01949844
- Conditions
- Coronary Artery Disease; CAD
- Interventions
- regadenoson; Optimark®; Myocardial perfusion MRI
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2014-05-16
- Completion
- 2017-10-23
- Enrolment
- 44
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCoronary Artery Disease; CADInterventionregadenoson; Optimark®; Myocardial perfusion MRIPhaseNot applicableRegistry statusCompletedRegadenoson Stress-MRI to Identify Coronary Artery Disease in Atrial Fibrillation Patients
NCT01710254 · start 2013-01
Registered record
- Registry ID
- NCT01710254
- Conditions
- Atrial Fibrillation; Coronary Artery Disease
- Interventions
- Regadenoson MRI; Gadobenate dimeglumine
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2013-01
- Completion
- 2016-10
- Enrolment
- 30
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAtrial Fibrillation; Coronary Artery DiseaseInterventionRegadenoson MRI; Gadobenate dimegluminePhasePhase 2Registry statusCompletedRegadenoson and Adenosine
NCT01809743 · start 2013-01
Registered record
- Registry ID
- NCT01809743
- Conditions
- Coronary Artery Disease
- Interventions
- Regadenoson central -central; Regadenoson peripheral - peripheral; Regadenoson central - peripheral; Regadenoson peripheral - central; Adenosine
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2013-01
- Completion
- 2013-10
- Enrolment
- 100
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCoronary Artery DiseaseInterventionRegadenoson central -central; Regadenoson peripheral - peripheral; Regadenoson central - peripheral; Regadenoson peripheral - central +1 morePhasePhase 3Registry statusCompletedComparison of Quantitative MRI Perfusion Methods With Quantitative PET Perfusion Imaging
NCT02608944 · start 2012-09-30
Registered record
- Registry ID
- NCT02608944
- Conditions
- MRI Scans
- Interventions
- Adenosine; Regadenoson; O-15 labeled radioactive water; MRI; PET Imaging
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Withdrawn
- Start
- 2012-09-30
- Completion
- 2019-06-12
- Enrolment
- 0
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMRI ScansInterventionAdenosine; Regadenoson; O-15 labeled radioactive water; MRI +1 morePhaseNot applicableRegistry statusWithdrawnAbsolute Quantification of Coronary Flow Reserve by Stress Perfusion MRI
NCT01655043 · start 2012-09
Registered record
- Registry ID
- NCT01655043
- Conditions
- Myocardial Ischemia
- Interventions
- Regadenoson; gadofoveset trisodium
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2012-09
- Completion
- 2014-02
- Enrolment
- 20
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMyocardial IschemiaInterventionRegadenoson; gadofoveset trisodiumPhasePhase 2Registry statusCompletedMicrovascular Blood Flow in Sickle Cell Anemia
NCT01566890 · start 2012-07
Registered record
- Registry ID
- NCT01566890
- Conditions
- Sickle Cell Disease; Sickle Cell Anemia
- Interventions
- regadenoson infusion with contrast-enhanced ultrasound; contrast-enhanced ultrasound; contrast-enhanced ultrasound; contrast-enhanced ultrasound; contrast-enhanced ultrasound
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2012-07
- Completion
- 2020-11-16
- Enrolment
- 91
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSickle Cell Disease; Sickle Cell AnemiaInterventionregadenoson infusion with contrast-enhanced ultrasound; contrast-enhanced ultrasound; contrast-enhanced ultrasound; contrast-enhanced ultrasound +1 morePhaseNot applicableRegistry statusCompleted