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High dose Atorvastatin+enoxaparin

Hallym University Medical Center · FDA-approved active Small molecule

This combination reduces cholesterol synthesis via statin activity while simultaneously inhibiting thrombin and factor Xa to prevent blood clot formation.

This combination reduces cholesterol synthesis via statin activity while simultaneously inhibiting thrombin and factor Xa to prevent blood clot formation. Used for Acute coronary syndrome with hyperlipidemia, Secondary prevention of cardiovascular events in high-risk patients.

At a glance

Generic nameHigh dose Atorvastatin+enoxaparin
SponsorHallym University Medical Center
Drug classStatin + Low-molecular-weight heparin combination
TargetHMG-CoA reductase (atorvastatin); Factor IIa and Factor Xa (enoxaparin)
ModalitySmall molecule
Therapeutic areaCardiovascular
PhaseFDA-approved

Mechanism of action

Atorvastatin (a statin) competitively inhibits HMG-CoA reductase, the rate-limiting enzyme in cholesterol biosynthesis, thereby lowering LDL cholesterol and reducing atherosclerotic plaque formation. Enoxaparin is a low-molecular-weight heparin that potentiates antithrombin III, inactivating factors IIa and Xa to prevent thrombosis. Together, they address both lipid management and acute anticoagulation in cardiovascular disease.

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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