Cangrelor
FDA-approved product (powder, intravenous), marketed as Cangrelor, Kengreal.
- Registered studies
- 45
- Lab records
- 0
- Pathogens at ≥40%
- 3 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Myocardial infarction
- Percutaneous Coronary Intervention
- Recurrent thrombophlebitis
Indications ChEMBL records as approved, from FDA and DailyMed labels. Label ↗
- WHO therapeutic group
- Platelet aggregation inhibitors excl. heparin
- FDA pharmacologic class
- P2Y12 Platelet 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 M. tuberculosis, MRSA 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- MRSA44.3% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- E. coli45.9% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- K. pneumoniae36.0% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- M. tuberculosis44.8% 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
45registered studies name this medicine, for any condition. 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 Cangrelor 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.
- DichlorphenamideExisting use: Glaucoma73.9% AI-predicted activityagainst M. tuberculosisLab records exist2 registered studies
- Tamsulosin HydrochlorideExisting use: Benign prostatic hyperplasia, Prostate carcinoma73.2% AI-predicted activityagainst M. tuberculosis50+ registered studies
- Thiethylperazine MalateExisting use: Allergic disease71.8% AI-predicted activityagainst M. tuberculosisNo documented evidence found
- SaquinavirExisting use: HIV infection, HIV-1 infection, Viral disease71.5% AI-predicted activityagainst M. tuberculosis50+ registered studies
- AvacopanExisting use: Anti-neutrophil antibody associated vasculitis, Anti-neutrophil cytoplasmic antibody-associated vasculitis, Granulomatosis with Polyangiitis and 1 more71.3% AI-predicted activityagainst M. tuberculosis26 registered studies
- Lasmiditan SuccinateExisting use: Migraine disorder71.0% AI-predicted activityagainst M. tuberculosisNo documented evidence found
- SotorasibExisting use: Neoplasm, Non-small cell lung carcinoma71.0% AI-predicted activityagainst M. tuberculosis50+ registered studies
- Vinblastine SulfateExisting use: Classic Hodgkin lymphoma, Fungal infectious disease, Hodgkins lymphoma and 3 more70.8% AI-predicted activityagainst M. tuberculosis50+ registered studies
- Haloperidol DecanoateExisting use: Conduct disorder, Mental or behavioural disorder, Psychosis and 4 more70.1% AI-predicted activityagainst M. tuberculosis50+ registered studies
- HydrochlorothiazideExisting use: Angina pectoris, Cardiovascular disease, Chronic kidney disease and 9 more70.1% AI-predicted activityagainst M. tuberculosis50+ registered studies
- TolvaptanExisting use: Autosomal dominant polycystic kidney disease, Cardiovascular disease, Congestive heart failure and 4 more70.0% AI-predicted activityagainst M. tuberculosis50+ registered studies
- Larotrectinib SulfateExisting use: Abdominal Neoplasms, Cancer, Metastasis and 1 more69.2% AI-predicted activityagainst M. tuberculosis5 registered studies
Registered studies
A registration describes a study; it does not establish a positive result.
Cangrelor Neonatal PK/PD and Safety Study
NCT02765633 · start 2017-01-03
Registered record
- Registry ID
- NCT02765633
- Conditions
- Partial Obstruction of Systemic to Pulmonary Artery Shunt; Complete Obstruction of Systemic to Pulmonary Artery Shunt
- Interventions
- Cangrelor
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2017-01-03
- Completion
- 2019-12-23
- Enrolment
- 22
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPartial Obstruction of Systemic to Pulmonary Artery Shunt; Complete Obstruction of Systemic to Pulmonary Artery ShuntInterventionCangrelorPhasePhase 1Registry statusCompletedCangrelor in ST-Elevation Myocardial Infarction to Decrease Infarct Size
NCT03043274 · start 2017-01
Registered record
- Registry ID
- NCT03043274
- Conditions
- STEMI - ST Elevation Myocardial Infarction
- Interventions
- Cangrelor
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Terminated
- Start
- 2017-01
- Completion
- 2019-05
- Enrolment
- 23
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSTEMI - ST Elevation Myocardial InfarctionInterventionCangrelorPhasePhase 4Registry statusTerminatedThe Effect of IV Cangrelor and Oral Ticagrelor Study
NCT02733341 · start 2016-07-21
Registered record
- Registry ID
- NCT02733341
- Conditions
- Acute Coronary Syndrome (ACS); High On-treatment Platelet Reactivity (HTPR); Microvascular Obstruction (MVO); ST-segment Elevation Myocardial Infarction (STEMI); Thrombolysis in Myocardial Infarction (TIMI); Unstable Angina (UA)
- Interventions
- Cangrelor; Ticagrelor
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2016-07-21
- Completion
- 2018-10-01
- Enrolment
- 100
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAcute Coronary Syndrome (ACS); High On-treatment Platelet Reactivity (HTPR); Microvascular Obstruction (MVO); ST-segment Elevation Myocardial Infarction (STEMI) +2 moreInterventionCangrelor; TicagrelorPhasePhase 4Registry statusCompletedPlatelet Function in Resuscitated Patients-2
NCT03445546 · start 2016-05-01
Registered record
- Registry ID
- NCT03445546
- Conditions
- Acute Myocardial Infarction; Cardiac Arrest
- Interventions
- diagnostic test of platelet function
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2016-05-01
- Completion
- 2018-05-15
- Enrolment
- 25
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAcute Myocardial Infarction; Cardiac ArrestInterventiondiagnostic test of platelet functionPhaseNot recordedRegistry statusCompletedIn Vitro Pharmacodynamic Effects of Cangrelor in Ticagrelor Treated Patients
NCT02081443 · start 2014-04
Registered record
- Registry ID
- NCT02081443
- Conditions
- Coronary Artery Disease
- Interventions
- Ticagrelor 180mg; Ticagrelor 90mg
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2014-04
- Completion
- 2015-10
- Enrolment
- 60
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCoronary Artery DiseaseInterventionTicagrelor 180mg; Ticagrelor 90mgPhaseNot applicableRegistry statusCompletedCangrelor to Clopidogrel or Prasugrel Transition Study
NCT01979445 · start 2013-12-02
Registered record
- Registry ID
- NCT01979445
- Conditions
- Coronary Artery Disease (CAD)
- Interventions
- Cangrelor; Clopidogrel; Prasugrel
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2013-12-02
- Completion
- 2014-01-20
- Enrolment
- 15
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCoronary Artery Disease (CAD)InterventionCangrelor; Clopidogrel; PrasugrelPhasePhase 2Registry statusCompletedCangrelor Prasugrel Transition Study
NCT01852019 · start 2013-06
Registered record
- Registry ID
- NCT01852019
- Conditions
- Coronary Artery Disease
- Interventions
- Cangrelor; Prasugrel
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2013-06
- Completion
- 2013-07
- Enrolment
- 12
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCoronary Artery DiseaseInterventionCangrelor; PrasugrelPhasePhase 2Registry statusCompletedCangrelor Ticagrelor Transition Study
NCT01766466 · start 2013-01
Registered record
- Registry ID
- NCT01766466
- Conditions
- Coronary Artery Disease
- Interventions
- cangrelor; Ticagrelor
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2013-01
- Completion
- 2013-02
- Enrolment
- 12
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCoronary Artery DiseaseInterventioncangrelor; TicagrelorPhasePhase 2Registry statusCompletedA Clinical Trial Comparing Cangrelor to Clopidogrel Standard Therapy in Subjects Who Require Percutaneous Coronary Intervention (PCI) (CHAMPION PHOENIX)
NCT01156571 · start 2010-09
Registered record
- Registry ID
- NCT01156571
- Conditions
- Atherosclerosis; Percutaneous Coronary Intervention; Acute Coronary Syndrome
- Interventions
- cangrelor P2Y12 (platelet) inhibitor; Clopidogrel - 300 or 600 mg (study arm); Clopidogrel 600 mg post cangrelor
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2010-09
- Completion
- 2012-12
- Enrolment
- 11,145
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAtherosclerosis; Percutaneous Coronary Intervention; Acute Coronary SyndromeInterventioncangrelor P2Y12 (platelet) inhibitor; Clopidogrel - 300 or 600 mg (study arm); Clopidogrel 600 mg post cangrelorPhasePhase 3Registry statusCompletedMaintenance of Platelet Inhibition With Cangrelor
NCT00767507 · start 2008-10
Registered record
- Registry ID
- NCT00767507
- Conditions
- Acute Coronary Syndrome (ACS)
- Interventions
- cangrelor; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2008-10
- Completion
- 2011-07
- Enrolment
- 221
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAcute Coronary Syndrome (ACS)Interventioncangrelor; PlaceboPhasePhase 2Registry statusCompletedAssess the Effect of Cangrelor at the Therapeutic Dose and a Supratherapeutic Dose Level on the QT/QTc Interval in Healthy Volunteers
NCT00699504 · start 2008-06
Registered record
- Registry ID
- NCT00699504
- Conditions
- Healthy
- Interventions
- cangrelor; cangrelor; cangrelor; moxifloxacin; placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2008-06
- Completion
- 2008-11
- Enrolment
- 67
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHealthyInterventioncangrelor; cangrelor; cangrelor; moxifloxacin +1 morePhasePhase 1Registry statusCompletedAspirin Resistance and Percutaneous Coronary Intervention (PCI)
NCT01103440 · start 2007-04
Registered record
- Registry ID
- NCT01103440
- Conditions
- Stable Angina
- Interventions
- Intravenous Glycoprotein inhibitor + ASA, Clopidogrel; Antiplatelet Therapy (ASA, Clopidogrel)
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2007-04
- Completion
- 2009-06
- Enrolment
- 36
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionStable AnginaInterventionIntravenous Glycoprotein inhibitor + ASA, Clopidogrel; Antiplatelet Therapy (ASA, Clopidogrel)PhasePhase 2Registry statusCompletedCangrelor Versus Standard Therapy to Achieve Optimal Management of Platelet Inhibition.
NCT00385138 · start 2006-09
Registered record
- Registry ID
- NCT00385138
- Conditions
- Atherosclerosis; Acute Coronary Syndrome (ACS)
- Interventions
- Cangrelor; clopidogrel; Placebo bolus & placebo infusion; Placebo capsules - end of PCI; Placebo capsules - end of infusion
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Terminated
- Start
- 2006-09
- Completion
- 2010-06
- Enrolment
- 5,364
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAtherosclerosis; Acute Coronary Syndrome (ACS)InterventionCangrelor; clopidogrel; Placebo bolus & placebo infusion; Placebo capsules - end of PCI +1 morePhasePhase 3Registry statusTerminatedA Clinical Trial to Demonstrate the Efficacy of Cangrelor
NCT00305162 · start 2006-04
Registered record
- Registry ID
- NCT00305162
- Conditions
- Myocardial Infarction (MI); Acute Coronary Syndromes (ACS)
- Interventions
- Cangrelor (P2Y12 inhibitor); clopidogrel (oral P2Y12 inhibitor); Placebo bolus & placebo infusion; Placebo capsules - end of infusion; Placebo capsules - as soon as possible after randomization
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Terminated
- Start
- 2006-04
- Completion
- 2010-06
- Enrolment
- 8,882
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMyocardial Infarction (MI); Acute Coronary Syndromes (ACS)InterventionCangrelor (P2Y12 inhibitor); clopidogrel (oral P2Y12 inhibitor); Placebo bolus & placebo infusion; Placebo capsules - end of infusion +1 morePhasePhase 3Registry statusTerminatedPharmacokinetics/Pharmacodynamics (PK/PD) of Cangrelor
NCT00102674 · start 2005-03
Registered record
- Registry ID
- NCT00102674
- Conditions
- Healthy
- Interventions
- cangrelor
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2005-03
- Completion
- 2005-05
- Enrolment
- 40
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHealthyInterventioncangrelorPhasePhase 1Registry statusCompleted