A One
Dose Future

Why should you participate?
At Verve, we are committed to developing a new approach to address this unmet need. By taking part in a clinical trial you may help improve treatment options for others that have high LDL-C levels. Take the prescreener or click on one of our clinical trials below to learn more.
See if you prequalify
Your information is stored in a HIPAA-compliant database and provided to the trial sites for follow-up as appropriate. For further information, please see our privacy policy page.
See if you prequalify
Your information is stored in a HIPPA-compliant database and provided to the trial sites for follow-up as appropriate. For further information, please see our privacy policy page.

Information about our studies
Understanding cardiovascular health
Some risk factors that impact your heart health are things you cannot change:
- Age – CVD risk increases with age
- Race and ethnicity – Some groups may have higher risk of certain conditions such as diabetes, which increase the risk of CVD
- Genetics – family history and genetic conditions may increase risk of CVD
Others risk factors are changeable. Your risk of CVD may be reduced by lifestyle changes such as:
- Maintaining a healthy weight
- Exercising regularly
- Managing blood sugar levels
- Not smoking
- Following a heart healthy diet
- Managing blood pressure
- Getting enough sleep
About our clinical trials

The Heart-2 study is a clinical trial for people who have high levels of LDL-C despite being on cholesterol-lowering medicines and have been diagnosed with the following:
Heterozygous familial hypercholesterolemia (HeFH), an inherited condition that causes lifelong high LDL-C levels.
and/or
Premature coronary artery disease (CAD), which is a serious heart disease because of high cholesterol, occurring before the age of 65 in women or 55 in men.
The purpose of the Heart-2 study is to assess the safety and tolerability of the investigational medicine called VERVE-102 and see if it can help lower LDL-C levels with a single dose.


Understanding clinical trials
How new approved medicines are developed



- Evaluate safety and side effects
- Determine a safe dosage range
- Assess tolerability



- Evaluate effectiveness
- Evaluate safety and side effects
- Confirm dosage



- Confirm effectiveness
- Monitor adverse reactions
- Compare with standard treatments



- Collect long-term data
- Identify rare side effects
- Ensure ongoing safety