CREATING BETTER HEALTH CARE TOGETHER
WHAT IS A CLINICAL TRIAL?
In a clinical trial, participants are provided investigational medication under physician and other research professional supervision. This investigational medication has not received approval by health organizations such as US Food and Drug Administration (FDA). Clinical trials are overseen by an ethics committee or an institutional review board (IRB) who prioritizes participant safety, welfare and rights.
WHAT SHOULD I EXPECT?
Volunteers will be provided a informed consent form (ICF) which provides a detailed explanation regarding study participation. Volunteers will be given ample time to review this information and an opportunity to ask questions. Qualifying participants will be allowed to participate in the clinical trial.
Once enrolled, participants will attend scheduled visits and perform study activities relevant to the clinical trial.