Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 3:32 AM
Ignite Modification Date:
2025-12-25 @ 3:32 AM
NCT ID:
NCT06391905
Eligibility Criteria:
Inclusion Criteria:
1. Age 18-75 years old, gender is not limited, and signed informed consent;
2. Histologically confirmed colorectal adenocarcinoma with pMMR/MSS;
3. Colorectal cancer with distant metastasis or inability to be radically surgically resected as assessed by imaging examination Patient;
4. Immunohistochemistry or sequencing to evaluate the high expression status of PCSK9 in tumors;
5. ECOG score 0-1;
6. Expected survival ≥ 3 months.
Exclusion Criteria:
1. Hypocholesterolemia, hypolipidemia and its family history, previous allergic reaction to PCSK9 inhibitors History of allergic reaction to PCSK9 inhibitors;
2. preoperative pathological diagnosis of advanced colorectal adenocarcinoma without pMMR/MSS, with the chance of radical surgical treatment;
3. Hypolipidemia caused by combination with other long-term lipid-lowering drugs;
4. malignancies other than colorectal cancer with negligible risk of metastasis or death (e.g., expected 5-year OS \>90%) within 5 years prior to enrollment and for which a radical outcome is expected after treatment (e.g., adequately treated carcinoma in situ of the uterine cervix, basal or squamous cell skin cancers, limited prostate cancers treated for radical purposes, ductal carcinomas in situ treated for radical purposes surgically), with the exception of (b) the following;
5. history of autoimmune diseases, including but not limited to myasthenia gravis, myositis, autoimmune hepatitis;
6. major surgery within 4 weeks prior to enrollment or incomplete recovery from previous surgery;
7. systemic immunostimulatory drug therapy (including but not limited to interferon or IL-2) within 4 weeks or 5 half-lives of the drug, whichever is shorter, prior to enrollment;
8. pre-existing or clinically significant CNS disease at screening, such as epilepsy, seizures, paralysis, aphasia, stroke, severe brain injury, dementia, Parkinson's disease, cerebellar disease, organic brain syndromes, or psychiatric disorders;
9. receipt of systemic corticosteroids (\>10 mg/d prednisone equivalent) or other systemic immunosuppressants, etc. within 2 weeks prior to randomization;
10. previous allogeneic bone marrow transplantation or previous solid organ transplantation;
11. subjects who, in the judgment of the Investigator, have any factors affecting compliance with the protocol, including uncontrollable medical, psychological, familial, sociological, or geographic conditions; or who are unwilling or unable to comply with the procedures required in the study protocol;
12. history of idiopathic pulmonary fibrosis, drug-induced pneumonia, organic pneumonia (i.e., occlusive bronchiolitis), idiopathic pneumonia, or evidence of active pneumonia on CT scan of the chest at the time of screening; 13. receipt of any live vaccine (e.g., vaccines against infectious diseases such as influenza vaccine, varicella vaccine, etc.) within 4 weeks (28 days) prior to randomization
14\. Pregnant or lactating female patients;
15\. Hypersensitivity to fluorouracil-based or platinum-based agents or their excipients.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
85 Years
Study:
NCT06391905
Study Brief:
Protocol Section:
NCT06391905