Now enrolling · 5 studies open→

Help move medicine forward. We’ll take care of you.

Join a clinical study close to home, led by a cardiologist and a research team that puts your safety and comfort first. You can leave at any time.

How it works
3 simple stepsReach out, talk with our team, then you decide.
Led byA cardiologist
Research sites
6 in California
New clinic
5 rooms ready
Trusted by research sponsors
Novo Nordisk
  • IRB-reviewedEvery study approved by an independent ethics board
  • Cardiologist-ledResearch directed by a practicing cardiologist
  • Private & secureYour health information stays protected
  • 6 local sitesCare close to home in Southern & Central California
Now enrolling

Find a study that fits you.

Each study has its own requirements. Read who it is for, then tap Check eligibility and our team will walk you through it.

Cardiology · After a heart attack

Heart Attack Recovery Study

For people who had a heart attack in the past 4 weeks. Studies whether an investigational medicine taken at home can help protect the heart after a heart attack.

Age 18+Heart attack ≤ 4 weeks ago2+ blocked arteries
Check eligibility →
Prevention · Lipoprotein(a)

Elevated Lp(a) & Heart Health Study

For people with high Lp(a) who have never had a heart attack, stroke, stent or bypass. Studies whether an investigational medicine can lower Lp(a).

Age 50+High Lp(a)No prior heart event
Check eligibility →
Heart failure · Weight

Heart Failure and Weight Management Study

For adults living with heart failure who also carry extra weight.

Age 18+Heart failureBMI 30+
Check eligibility →
Vascular · Leg circulation

PAD Walking Study

For people with peripheral artery disease who have leg pain or trouble walking long distances.

Age 18+PAD diagnosisLeg pain when walking
Check eligibility →
Heart failure · Advanced

Advanced Heart Failure Study

For people with heart failure for at least 6 months and an implanted defibrillator (ICD).

Age 18–85Ejection fraction ≤ 35%Has an ICD
Check eligibility →
How it works

Three steps. No obligation.

Joining a study starts with a conversation. Nothing is decided until you say so.

  1. 01

    Reach out

    Send the short form, or call or text us. Tell us which study caught your eye.

    Form, call or text
  2. 02

    Talk with our team

    A research team member calls you back, answers your questions and checks whether the study fits.

    A friendly phone call
  3. 03

    You decide

    Take the time you need. Joining is your choice, and you can leave at any time.

    Your choice, always
Start with step 1 →Talking with us doesn’t commit you to anything.
Our commitment

Informed. Guided. Never on your own.

From your first call, our research team explains the study in plain language, gives you printed information to take home, and walks you through every visit. Questions are always welcome.

Your study visit
  • Study brochure to take homePlain-language guide to the study
  • Consent explained, step by stepBefore anything starts
  • A coordinator guides your visitEvery step, every visit
  • Your questions answeredBefore, during and after
Free to leave at any time · Ethics-board reviewed
We inform you

Printed brochures and study guides you can read at home and share with family.

We guide you

A research coordinator walks you through each step and every visit.

We answer your questions

Call or text our team with any question, before, during and after the study.

Never rushed

Take the time you need to decide. Joining is always your choice.

CENTRAL VALLEYLOS ANGELES COUNTYSAN BERNARDINO MTNSBakersfieldMission HillsVan Nuys · HQAlhambraInglewoodLake Arrowhead
Six research sites

Close to home, across California.

From the San Fernando Valley to the Central Valley. The study team confirms which site works for you.

For sponsors & CROs

A new clinic space, ready for your next study.

Five new rooms, a full research team and modern equipment, all under one roof. We have the space and the people to start enrolling now.

Room 01Clinic photo coming soon
Room 02Photo coming soon
Room 03Photo coming soon
Room 04Photo coming soon
Room 05Photo coming soon
New clinic5 rooms ready
5
Rooms ready

A brand-new clinic space, set up for screening and study visits.

Fully staffed
Research team

A cardiologist PI, research nurses and coordinators already in place.

Fully equipped
Modern equipment

Everything a study visit needs, on site and ready to use.

6
Research sites

Van Nuys, Mission Hills, Inglewood, Alhambra, Bakersfield and Lake Arrowhead.

Therapeutic areas
CardiovascularHeart failureLipids · Lp(a)PADCardiometabolicPost-MI
A team you can trust

The people who will care for you.

Physicians, nurses and research coordinators who know volunteers by name and stay with them from the first call to the last visit.

Rodney Samaan, MD, MPH

Rodney Samaan, MD, MPH

Co-Founder · Principal Investigator

Cardiologist, founder of ProgressiveMD, and Chair of Medicine at Mission Community Hospital.

Andrew Young

Andrew Young

Co-Founder · Research Director

Oversees research and business operations across InvivoCure's sites.

Independent oversight

An IRB reviews every study before it starts and while it runs.

Informed consent, always

You get the full consent form and time to ask questions before agreeing.

Good Clinical Practice

Studies follow international GCP standards for safety and data quality.

Getting started4 questions
What is a clinical trial?

A research study that tests whether an investigational medicine or approach is safe and works. Every trial follows a written plan, and volunteers are watched closely by a medical team the whole time.

How do I find out if I qualify?

Pick a study and contact us. Only the study team can confirm eligibility, and they'll walk you through it on the phone.

Where do study visits happen?

At one of our six InvivoCure sites. The study team confirms which location works for your study.

Can I leave a study once I join?

Yes. Taking part is voluntary, and you can leave at any time.

Safety, cost & care4 questions
Who keeps volunteers safe?

An independent ethics board (an IRB) reviews and approves every study before it starts and keeps watching it while it runs. You’ll get a consent form that explains the risks and possible benefits before you agree to anything.

Does it cost anything? Will insurance be billed?

Answer pending from the study team.

Will I be paid for my time?

Answer pending from the study team.

Could I get a placebo?

Answer pending from the study team.