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Aspirin + Atorvastatin

Fundacion GESICA · FDA-approved active Small molecule

This combination reduces cardiovascular risk by inhibiting platelet aggregation (aspirin) and lowering LDL cholesterol (atorvastatin).

This combination reduces cardiovascular risk by inhibiting platelet aggregation (aspirin) and lowering LDL cholesterol (atorvastatin). Used for Secondary prevention of cardiovascular events in patients with established coronary artery disease or high cardiovascular risk, Primary prevention of myocardial infarction and stroke in high-risk patients.

At a glance

Generic nameAspirin + Atorvastatin
SponsorFundacion GESICA
Drug classAntiplatelet agent + HMG-CoA reductase inhibitor (statin)
TargetCyclooxygenase (COX) + HMG-CoA reductase
ModalitySmall molecule
Therapeutic areaCardiovascular
PhaseFDA-approved

Mechanism of action

Aspirin irreversibly inhibits cyclooxygenase (COX), preventing thromboxane A2 synthesis and platelet aggregation, thereby reducing thrombotic events. Atorvastatin is an HMG-CoA reductase inhibitor that lowers LDL cholesterol and reduces atherosclerotic plaque formation. Together, they provide complementary cardioprotective effects through antiplatelet and lipid-lowering mechanisms.

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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