Kengreal

Kengreal Uses, Dosage, Side Effects, Food Interaction and all others data.

Kengreal is an intravenous, direct-acting, reversible P2Y12 inhibitor for patients undergoing percutaneous coronary intervention (PCI) who have not been yet treated by oral P2Y12 inhibitors. An advantage Kengreal provides over oral P2Y12 inhibitors (such as prasugrel, ticagrelor, and clopidogrel) is that it is an active drug not requiring metabolic conversion therefore providing a rapid onset and offset of action. Kengreal was approved by the FDA in June 2015 for intravenous application.

Trade Name Kengreal
Availability Prescription only
Generic Cangrelor
Cangrelor Other Names Cangrelor
Related Drugs clopidogrel, Plavix, Integrilin, Angiomax, eptifibatide, bivalirudin
Type Intravenous
Formula C17H25Cl2F3N5O12P3S2
Weight Average: 776.35
Monoisotopic: 774.9483145
Protein binding

about 97-98%.

Groups Approved
Therapeutic Class
Manufacturer
Available Country United States,
Last Updated: September 19, 2023 at 7:00 am
Kengreal
Kengreal

Uses

Kengreal is a P2Y12 platelet receptor antagonist used during percutaneous coronary intervention to reduce the risk for periprocedural myocardial infarction (MI), repeat coronary revascularization, and stent thrombosis (ST).

For use as an adjunct to percutaneous coronary intervention (PCI) for reducing the risk of periprocedural myocardial infarction (MI), repeat coronary revascularization, and stent thrombosis (ST) in patients in who have not been treated with a P2Y12 platelet inhibitor and are not being given a glycoprotein IIb/IIIa inhibitor.

Kengreal is also used to associated treatment for these conditions: Post procedural myocardial infarction, Stent Thrombosis, Repeat coronary revascularization

How Kengreal works

Kengreal is a selective, reversible, P2Y12 platelet receptor antagonist which inhibits ADP platelet aggregation. ADP is typically released by damaged blood vessels, red blood cells, and/or platelets due to agonists stimulating platelet activity. ADP binds to P2Y12 to stimulate and complete platelet aggregation by inhibiting adenylyl cyclase by a Gi protein, thus potentiating dense granule secretion and increasing coagulation activity. Kengreal acts on the same target as oral irreversible inhibitors clopidogrel and ticlopidine and has a similar mechanism of action, but is reversible and provides a fast onset and offset of action.

Food Interaction

  • Avoid herbs and supplements with anticoagulant/antiplatelet activity. Examples include garlic, ginger, bilberry, danshen, piracetam, and ginkgo biloba.

Kengreal Disease Interaction

Major: bleeding

Volume of Distribution

In a study in healthy volunteers administration at a dose of 30 mcg/kg bolus plus 4 mcg/kg/min showed a volume of distribution of 3.9 L.

Half Life

The average elimination half-life of cangrelor is about 3-6 minutes.

Clearance

The mean clearance is about 43.2 L/h.

Elimination Route

Following IV administration of [3H] cangrelor, 58% of radioactivity was recovered in urine. The remaining 35% of radioactivity was in feces, presumably following biliary excretion.

Innovators Monograph

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*** Taking medicines without doctor's advice can cause long-term problems.
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