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:
2026-03-26 @ 3:15 PM
Ignite Modification Date:
2026-03-26 @ 3:15 PM
NCT ID:
NCT07391566
Eligibility Criteria:
Inclusion Criteria:
1. Able to provide a signed informed consent;
2. Age ≥ 18 years and ≤ 75 years, both male and female;
3. Histologically confirmed metastatic colorectal cancer (CRC) with RAS mutation;
4. Prior therapies for colorectal cancer:
(1 ) For phase 1b patients: who have failed or intolerable to prior first-line therapy; (2) For phase 2 patients: who have not received prior systemic therapy for metastatic colorectal cancer.
5\. At least one measurable lesion according to RECIST 1.1 criteria; 6. Eastern Cooperative Oncology Group (ECOG) score of 0 or 1; 7. Life expectancy≥ 6 months; 8. Adequate bone marrow and organ function; 9. Negative pregnancy test for women of childbearing potential. patients of childbearing potential should take effective contraceptive measures during study drug treatment and until 6 months after initiation of investigational product.
Exclusion Criteria:
1. Patients with known microsatellite instability (MSI-H) or mismatch repair deficiency (dMMR) who are suitable for immune checkpoint inhibitor therapy as assessed by the investigator;
2. Malignant tumors other than mCRC within 5 years before signing the informed consent;
3. Patients who did not recover from the AE of previous anti-tumor treatment to ≤ Grade 1;
4. Patients with body cavity effusion requiring local treatment or poorly controlled effusion;
5. Symptomatic brain metastasis, history of spinal cord compression or meningeal metastasis;
6. Underwent other therapeutic surgery other than diagnosis, biopsy, drainage, or expected to require major surgery during the study, or had unhealed wound, ulcer or fracture.
7. Current or previous uncontrolled concomitant non-gastrointestinal disease including, but not limited to myocardial infarction, unstable angina, coronary artery/peripheral artery bypass grafting, heart failure, cerebrovascular accident, transient ischemic attack, pulmonary embolism, deep vein thrombosis, serious arrhythmia, current uncontrolled hypertension, previous history of hypertensive crisis or hypertensive brain disease, tumor invasion into major blood vessels, interstitial lung disease, interstitial pneumonia, pulmonary interstitial fibrosis, reversible posterior leukoencephalopathy syndrome (RPLS), etc.;
8. Current or past presence of the gastrointestinal abnormalities, including but not limited to active peptic ulcer, clinically significant gastrointestinal abnormalities prior to informed consent, active colitis, long-term anticoagulant therapy, antiplatelet therapy, etc.;
9. Current or past significant risk of bleeding;
10. Use of prohibited medication or therapy within the specified time;
11. History of drug abuse or alcoholism;
12. Known hypersensitivity to any component of any investigational product;
13. Pregnant and lactating women;
14. Other conditions that may increase the risk of the study or interfere with study results, in the judgment of the investigator.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
75 Years
Study:
NCT07391566
Study Brief:
Protocol Section:
NCT07391566