Learn about this study
This Expanded Access Program (EAP) provides access to 89Zr-DFO-girentuximab (TLX250-CDx) for kidney cancer imaging in the United States. The program allows access to investigational products outside of a clinical trial to patients for whom there are no comparable or satisfactory alternate options.
Who can participate?
Participating in clinical research is a significant, personal decision. Before enrolling, the study team will fully explain the research and provide an Informed Consent Form that outlines possible benefits and risks. This is your chance to ask questions and consult with your doctor to determine if the study is right for you.
You may be able to participate if:
- You have imaging evidence of renal mass(es) obtained from conventional diagnostic imaging with CT or MRI
- Your healthcare provider determines that TLX250-CDx may be beneficial for your care
- You meet the eligibility criteria for the expanded access program
Each clinical study has its own guidelines for who can participate, called eligibility criteria. However, only the research study staff can determine if you qualify to enroll in the study.