CVD1 – Synexus
Help Us Advance Medicine for Those at Risk of Cardiac Events
Enroll now in a research study for Obese or Overweight Volunteers with heart disease, hypertension, Type 2 Diabetes, or high cholesterol. All study related assessments are provided at no cost. Compensation up to $125 per visit for qualified participants may be provided.

Participant Qualifications
- Obese or Overweight Adults
- 18+ years old
- Body Mass Index (BMI) of >30 kg/m2 or >27 kg/m2
- Type 2 Diabetes with at least 2 of the following: High blood pressure, taking cholesterol medication, low HDL cholesterol, or current smoker -OR- Established cardiovascular disease such as: heart attack, peripheral artery disease, stents or angioplasty of the heart, legs, or carotid, CABG, positive stress test, abnormal cardiac imaging, carotid endarterectomy)
- Smokers allowed
- Health status is further evaluated by reviewing medical history, screening assessments, and visit with physician
- Available and willing to commit to study visit structure
STUDY INFORMATION
- The purpose of the study is to evaluate the cardiovascular safety of study subjects receiving the investigational product compared with placebo and rule out excess risk of Major Adverse Cardiac Event (MACE)when given in combination with standard of care (real-world setting) to subjects with obesity or who are overweight and have an increased risk of adverse CV outcomes.
- The study drug is being developed as a potential treatment for weight loss.
- This is a research study, and your participation is voluntary. You may stop participating at any time.
Compensation
Compensation varies by study and may go up to $125 per visit.
Get Started Now!
If you are interested in learning more, please complete the contact form and we will follow up with more information.
Contact Us Now
If you are interested in participating, please complete the contact form. We will follow up with more information and schedule a screening visit to see if you qualify.
What to Expect from a Trial
Our representative will speak with you about your medical history. If you meet the criteria for a clinical trial, we will ask you to come to the clinic for a screening visit and consultation. During the screening visit, you will consult with a medical staff member about the details of the trial and discuss any known side effects associated with it. We will answer your questions about participating in the trial, and you will be asked to sign an informed consent form.

