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Aspirin and/or Atorvastatin

NYU Langone Health · FDA-approved active Small molecule

Aspirin and/or Atorvastatin is a Antiplatelet agent and HMG-CoA reductase inhibitor (statin) Small molecule drug developed by NYU Langone Health. It is currently FDA-approved for Secondary prevention of cardiovascular events (myocardial infarction, stroke), Primary prevention of cardiovascular disease in high-risk patients.

Aspirin inhibits platelet aggregation via COX inhibition, while atorvastatin reduces cholesterol synthesis by inhibiting HMG-CoA reductase, together reducing cardiovascular risk.

Aspirin inhibits platelet aggregation via COX inhibition, while atorvastatin reduces cholesterol synthesis by inhibiting HMG-CoA reductase, together reducing cardiovascular risk. Used for Secondary prevention of cardiovascular events (myocardial infarction, stroke), Primary prevention of cardiovascular disease in high-risk patients.

At a glance

Generic nameAspirin and/or Atorvastatin
SponsorNYU Langone Health
Drug classAntiplatelet agent and HMG-CoA reductase inhibitor (statin)
TargetCyclooxygenase (COX) and 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 competitively inhibits HMG-CoA reductase, the rate-limiting enzyme in cholesterol biosynthesis, lowering LDL cholesterol and reducing atherosclerotic plaque formation. This combination addresses both thrombotic and lipid-related mechanisms of cardiovascular disease.

Approved indications

Common side effects

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

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

Competitive intelligence

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Frequently asked questions about Aspirin and/or Atorvastatin

What is Aspirin and/or Atorvastatin?

Aspirin and/or Atorvastatin is a Antiplatelet agent and HMG-CoA reductase inhibitor (statin) drug developed by NYU Langone Health, indicated for Secondary prevention of cardiovascular events (myocardial infarction, stroke), Primary prevention of cardiovascular disease in high-risk patients.

How does Aspirin and/or Atorvastatin work?

Aspirin inhibits platelet aggregation via COX inhibition, while atorvastatin reduces cholesterol synthesis by inhibiting HMG-CoA reductase, together reducing cardiovascular risk.

What is Aspirin and/or Atorvastatin used for?

Aspirin and/or Atorvastatin is indicated for Secondary prevention of cardiovascular events (myocardial infarction, stroke), Primary prevention of cardiovascular disease in high-risk patients.

Who makes Aspirin and/or Atorvastatin?

Aspirin and/or Atorvastatin is developed and marketed by NYU Langone Health (see full NYU Langone Health pipeline at /company/nyu-langone-health).

What drug class is Aspirin and/or Atorvastatin in?

Aspirin and/or Atorvastatin belongs to the Antiplatelet agent and HMG-CoA reductase inhibitor (statin) class. See all Antiplatelet agent and HMG-CoA reductase inhibitor (statin) drugs at /class/antiplatelet-agent-and-hmg-coa-reductase-inhibitor-statin.

What development phase is Aspirin and/or Atorvastatin in?

Aspirin and/or Atorvastatin is FDA-approved (marketed).

What are the side effects of Aspirin and/or Atorvastatin?

Common side effects of Aspirin and/or Atorvastatin include Gastrointestinal bleeding or ulceration (aspirin), Muscle pain or myalgia (atorvastatin), Elevated liver enzymes (atorvastatin), Dyspepsia, Rhabdomyolysis (rare).

What does Aspirin and/or Atorvastatin target?

Aspirin and/or Atorvastatin targets Cyclooxygenase (COX) and HMG-CoA reductase and is a Antiplatelet agent and HMG-CoA reductase inhibitor (statin).

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