EXoPERT EMERALD Clinical Study

Prior treatment

• Subjects who are currently in active treatment for drug abuse.
• Subjects who have received any treatment related to lung, breast, colorectal, pancreatic, or ovarian nodules, such as hormones prior to entering the study.

Other illness

• Any history of cancer diagnosed and treated within 5 years prior to the date of consent.
• Subjects with a history of previous cancer treatment via surgical resection, hormonal cancer treatment, chemotherapy, radiotherapy within the past 6 months for recent cancer diagnosis.
• Subjects who have any history of an allogeneic bone marrow, stem cell transplant, or solid organ transplant.
• Subjects who have consented and have undergone treatment in any other cancer related clinical trials withinthe past 6 months.

Other

• Subjects who are pregnant or breastfeeding women.
• Unsuitable sample for testing due to contamination, hemolysis, etc.

• Subject aged 45 years or older with a biopsy-proven or clinically suspected primary lung, breast, colorectal, pancreatic, or ovarian cancer, based on objective findings such as radiological, serological, endoscopic, or cytological findings, whose blood was collected prior to any systemic or definitive therapy for the cancer.
• Subjects who are willing and able to provide written informed consent.
• Subjects who are willing and able to comply with the study requirements.