The project relies on the participation of patients to existing cohorts, biobanks and a dedicated observation clinical study. All samples and data are collected after informed consent of participants. We thank volunteers for their participation to research.

As a participant of a clinical study, you have the right to stop your participation at any time with no justification and without healthcare consequences. You may access, verify and correct your personal data and withdraw your authorization to process such data at any time without justification. These rights apply to on-going clinical studies and studies based on data reuse.

To claim these rights, please contact the study investigator who knows your identity or the data protection officer (DPO).