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Acetylsalicylic Acid + clopidogrel

Hospital Universitari Vall d'Hebron Research Institute · FDA-approved active Small molecule

This combination inhibits platelet aggregation through two complementary pathways: acetylsalicylic acid irreversibly inhibits cyclooxygenase to block thromboxane A2 production, while clopidogrel blocks the P2Y12 adenosine diphosphate receptor.

This combination inhibits platelet aggregation through two complementary pathways: acetylsalicylic acid irreversibly inhibits cyclooxygenase to block thromboxane A2 production, while clopidogrel blocks the P2Y12 adenosine diphosphate receptor. Used for Acute coronary syndrome, Secondary prevention of cardiovascular events post-percutaneous coronary intervention, Stroke prevention in patients with acute ischemic stroke or transient ischemic attack.

At a glance

Generic nameAcetylsalicylic Acid + clopidogrel
SponsorHospital Universitari Vall d'Hebron Research Institute
Drug classDual antiplatelet agent
TargetCyclooxygenase-1 (COX-1) and P2Y12 receptor
ModalitySmall molecule
Therapeutic areaCardiovascular
PhaseFDA-approved

Mechanism of action

Acetylsalicylic acid (aspirin) prevents platelet activation by irreversibly acetylating cyclooxygenase-1, reducing thromboxane A2 synthesis. Clopidogrel is a thienopyridine that irreversibly blocks the P2Y12 ADP receptor on platelets, preventing platelet aggregation through a different mechanism. Together, they provide dual antiplatelet therapy with synergistic effects to prevent thrombotic events.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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