Volunteer to help advance medical science
We are continuously conducting new studies. The list changes often, so the most accurate answer comes from our team directly.

The five stages in detail
What happens at each point, from your first call to your final visit.
Pre-screening
We review the study's inclusion and exclusion criteria with you and check other suitability questions. This may include a short telephone interview.
Screening
You receive the study's Informed Consent Form and meet the study doctors and the clinical coordinator. A physical assessment and a review of your medical history are typically required, and there may be a waiting period before the next step.
Randomization
Once you qualify, treatment begins. You are randomly assigned to one of the study's interventions, which may include a placebo. Neither you nor your doctor will know which one you receive.
Treatment period
We monitor your progress and evaluate any adverse events throughout. Depending on the study, this can include follow-up visits, laboratory tests, and EKGs.
End of treatment
When the trial is complete, you come in for a final safety visit with laboratory tests, a physical assessment, and documentation of any adverse events.
Register for future studies
Not a match for a current study? Leave your name and phone in our registry and a coordinator will contact you when a new study fits.
Find out if you qualify. A coordinator will call you back.
Send your details and we will tell you which studies are enrolling and what the next step is.
