Participation in a clinical trial may provide access to investigational treatments before they become widely available. Depending on your type of cancer, previous treatments, and overall health, you may be eligible for certain studies at various points in your care.
Clinical trials follow strict protocols to help protect participants and gather reliable information. These studies are typically reviewed by regulatory agencies, such as the U.S. Food and Drug Administration (FDA), and independent ethics committees before they begin
enrolling participants.
Why are clinical trials important?
Clinical trials are foundational to the development of new medicines. These rigorous studies drive advancements that shape healthcare and determine the safety and effectiveness of medicines. Results from clinical trials help healthcare professionals take informed approaches to care.
Why is it important to have a diverse population participating in clinical trials?
A diverse clinical trial population is key to understanding how medicines may affect different people. This ensures that trial results are applicable to as many people as possible who are affected by the health condition being studied.

