Clinical research studies, or clinical trials, help scientists, doctors, and patient participants explore whether a drug is safe and effective for people. Before any drug can be approved and made available to the public, it must go through several phases of clinical research. Individuals who participate in clinical trials may not only benefit from the study themselves but may help the next generation of cancer patients have access to more effective and potentially life-saving therapies.
Before enrolling in a clinical trial, you must sign an Informed Consent Form (ICF). The ICF contains information about the clinical trial, including study goals, how long the clinical trial will last, benefits and risks, and the tests and procedures you will receive.
Clinical trial participation usually involves visiting a clinic regularly, taking or receiving the medicine that is being studied, and having assessments to monitor your health. You can still see your regular doctor, but you should let them know that you are participating in a study.
Participation in a clinical trial is your choice, and you may stop at any time.
If you have additional questions about participating in a clinical research study, contact a study center near you.
