If you decide to join, you’ll first be asked to sign an Informed Consent Form that describes all study procedures, potential risks, and your rights. Our study team will walk you through everything and answer your questions before you enroll.
After giving consent, participants undergo screening to check eligibility, including lab tests, imaging, and a review of prior treatment and surgical pathology. Those who qualify are then randomized into one of the two study arms: the combination therapy group or the physician’s-choice group.
During the trial, you’ll attend regular follow-up visits. These will include physical exams, blood work, check-ins on side effects, and possibly imaging or other assessments. The care is conducted by experienced oncology specialists, and all study-related procedures are provided at no cost.
* Study-related care is offered at no charge. Expert physicians and healthcare professionals conduct thorough physical exams and assessments.
