Drug intelligence / Profile preview

ticagrelor + prasugrel

Development stage
Preclinical
Lead developer
AstraZeneca
Modality
Small Molecules
Administration
Oral
01

Overview

Ticagrelor + prasugrel is a combination of two oral antiplatelet agents, both of which are P2Y12 receptor antagonists. Ticagrelor is a cyclopentyltriazolopyrimidine that binds reversibly to the platelet P2Y12 ADP receptor, inhibiting ADP-mediated platelet activation and aggregation. Prasugrel is a thienopyridine prodrug that irreversibly inhibits the same receptor after metabolic activation. Both drugs are used to reduce the risk of thrombotic cardiovascular events in patients with acute coronary syndromes (ACS), particularly those undergoing percutaneous coronary intervention (PCI). While each drug alone has demonstrated efficacy in preventing myocardial infarction and stroke, their combined use as dual P2Y12 inhibition increases bleeding risk compared to monotherapy and is not standard clinical practice; such combinations have been studied primarily for research purposes or in specific high-risk scenarios[4][5][6].

Other names
ticagrelor + prasugrel
02

Targets

P2Y12 (Purinergic P2Y12 receptor)

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