Participation In a Clinical Trial

Each clinical trial is designed to treat a certain group of people with a specific medical condition. Each participant must be screened to ensure they meet the clinical trials strict criteria.

Once a participant is deemed eligible, they can start the clinical trial treatment plan. The study doctors, providers, nurses, and other clinical trial staff monitor participants very closely through frequent visits, labs, imaging, and other tests to ensure participant safety and the effectiveness of the treatment.

The clinical trial team collects information from trial participants and reports it to the clinical trial sponsor. All information reported to the clinical trial sponsor is in accordance with Heath Information Portability and Accountability Act (HIPAA). The sponsor interprets the data from each participant to determine the overall safety and effectiveness.