The AZURE-Outcomes Study Are you at risk for, or

have a history of, high LDL,

heart disease, or stroke?
Check Eligibility
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Study Overview

The AstraZeneca “AZURE-Outcomes” study is testing a potential new oral, once a day, drug  to learn whether it can help lower bad cholesterol and reduce the risk of heart and blood vessel disease in adults who:

  • Have a history of heart disease OR
  • Have blood vessel disease OR
  • Are at high risk for a first cardiovascular event, such as heart attack, stroke, or circulatory issues in the legs.

Qualified Participants May Receive:

  • Reimbursement for their travel
  • Study-related care at no cost.

 

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Contact Us:

Who Can Participate In The AZURE-Outcomes Study?

People With a Prior Cardiovascular Event:

Are you taking cholesterol-lowering medication?
Are you 18+ years old with a history of heart disease?
Have you had a stroke, heart attack, or procedure to improve blood flow to the legs?
Do you have high LDL ("bad") cholesterol?

People Who Have NOT Had a Cardiovascular Event, But Are at High Risk:

Are you taking cholesterol-lowering medication?
Are you a man 50+ with high LDL ("bad") cholesterol?
Are you a woman 55+ with high LDL ("bad") cholesterol?
Have evidence of artery disease due to plaque buildup or other risk factors?

Who Can Participate In The AZURE-Outcomes Study?

People With a Prior Cardiovascular Event:

Are you taking cholesterol-lowering medication?
Are you 18+ years old with a history of heart disease?
Have you had a stroke, heart attack, or procedure to improve blood flow to the legs?
Do you have high LDL ("bad") cholesterol?

People Who Have NOT Had a Cardiovascular Event, But are at High Risk:

Are you taking cholesterol-lowering medication?
Are you a man 50+ with high LDL ("bad") cholesterol?
Are you a woman 55+ with high LDL ("bad") cholesterol?
Have evidence of artery disease due to plaque buildup or other risk factors?

What Should I Expect?

Screening Visit

Before you begin the study drug, AZD0780, or placebo, you will complete screening – including consent, medical history, and testing to determine if the study is right for you. 

Randomization Visit

Participants are randomly assigned (50/50) to receive either the investigational study tablet or a matching placebo with no active medicine.

Treatment Phase

Should you qualify, your participation may last up to ~4.5 years. You’ll take either Investigational study drug (AZD0780) or matching placebo alongside your regular cholesterol medication. Participation is voluntary, and you can stop taking it at any time. 

Start the Application:

See If You’re Eligible for the AZURE-Outcomes Study