{
"info": {
"nct_id": "NCT05487248",
"official_title": "A Study of On-treatment CtDNA Changes in Chemo-refractory Colorectal Cancer Patients",
"inclusion_criteria": "1. Age ≥ 18 years old\n2. Male or female\n3. ECOG performance status ≤2\n4. Must have histologically or cytologically verified colorectal cancer adenocarcinoma\n5. Inoperable locally advanced or metastatic disease\n6. Presence of measurable disease (by RECIST criteria version 1.1) on baseline CT scan of the thorax/abdomen/pelvis or CT scan of the thorax and MRI of the abdomen/pelvis\n7. At least two prior systemic treatments for advanced/metastatic colorectal cancer including oxaliplatin and irinotecan-based therapy (adjuvant or neoadjuvant systemic chemotherapy will be considered if tumour progression was documented within 6 month of the last chemotherapy dose)\n8. Candidate for standard third-line or subsequent lines of therapy as per decision of the treating physician\n9. Life expectancy of at least 3 months\n10. Women of childbearing potential must have a negative serum pregnancy test done within 28 days prior to enrolment.\n11. Effective contraception is in place for women of childbearing potential.\n12. Completion of all necessary screening procedures within 28 days prior to enrolment.\n13. Availability of archived tumour tissue\n14. Signed Informed Consent form (ICF) obtained prior to any study related procedure.\n\n Inclusion criterion applicable to FRANCE only\n15. Affiliated to the French Social Security System\nHealthy volunteers allowed\nMust have minimum age of 18 Years",
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"miscellaneous_criteria": ""
},
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}