Before you participate in a clinical trial, a detailed description of the research study, as well as possible risks and benefits, will be provided in writing in an “informed consent document” and discussed with you. You will be asked to review and sign the informed consent document prior to participating. Your medical history will be reviewed, and you will be given a study-required medical exam and study-required laboratory tests. If you qualify, you may be enrolled in the study. Once enrolled, feel free to discuss your research care with the study doctor or research site staff at any time during the study.