Active Studies

Protocols open for enrollment at our West Palm Beach site. Each is conducted with informed consent and Institutional Review Board (IRB) oversight.

Sample processing in a research laboratory
Every study sample and data point is processed per protocol and Good Clinical Practice.
Protocols

Studies underway

If a study interests you, contact us: the eligibility evaluation is free and carries no obligation.

Frequently asked questions

The essentials about participating in a clinical study. Have another question? Call or write to us.

It is medical research that evaluates, under an approved protocol, whether a treatment or procedure is safe and effective. Every study follows Good Clinical Practice (GCP) and is overseen by an independent ethics board (IRB).

Each protocol has eligibility criteria (age, diagnosis, prior treatments, among others). Our team performs a free initial evaluation — by phone or at the site — to find out whether a study may be right for you.

Yes, at any time and without giving a reason. Participation is completely voluntary, and withdrawing never affects your regular medical care or your relationship with your doctor.

No. Study assessments, visits, and study medication are provided at no cost to the participant. Some studies also compensate for time and travel.

Yes. We provide transportation for participants who need it: we pick you up and take you back home for study visits, at no cost. Mention it during your initial evaluation and we will arrange it.

Your health information is handled according to HIPAA and the study protocol. Research data uses a code instead of your name, and only authorized staff can link it back to you.

Aggregate study results are reported to the sponsor and regulatory authorities. If anything relevant to your health is found during the study, the team will tell you directly.

Interested in one of these studies?

Tell us which one, and together we will check — at no cost — whether you meet the eligibility criteria.

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