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 @ 3:44 AM
Ignite Modification Date:
2025-12-25 @ 3:44 AM
NCT ID:
NCT04656002
Eligibility Criteria:
Inclusion Criteria:
1. Patients with histologically or cytologically confirmed gastric cancer, including gastric adenocarcinoma or GEJ adenocarcinoma.
2. Patients with metastatic or locally recurrent unresectable disease.
3. Patients with diseased lesions that can be measured using standard computed tomography (CT) or magnetic resonance imaging (MRI).
4. Patients who have experienced disease progression during or after primary therapy for metastatic disease.
5. Patients over 19 years of age.
6. All clinically significant toxic effects of previous chemotherapy, surgery, radiation therapy, or hormone therapy are rated ≤1 (or neuropathic Cases ≤2 grade) (excluding hair loss).
7. Patients with an Eastern Oncology Cooperative Group Performance Status (ECOG PS) score of 0 or 1.
8. Total bilirubin ≤1.5 mg/dL (25.65 µmol/L), and aspartic acid aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 3.0 x upper limit of normal (ULN; or 5.0 x with liver metastasis) Patients with adequate liver function as defined by ULN).
etc
Exclusion Criteria:
1. Patients previously receiving treatment targeting the TGF-β signaling pathway
2. Patients who previously received Taxane-based chemotherapy
3. Patients with recorded and/or symptomatic brain or meningeal metastases.
4. Patients who experienced Grade 3-4 GI bleeding within 3 months prior to enrollment.
5. Patients who have experienced arterial thromboembolic events including, but not limited to, myocardial infarction, transient ischemic attack, cerebrovascular attack, or unstable angina within 6 months prior to enrollment.
6. Ongoing or active infection, symptomatic congestive heart failure, unstable angina, symptomatic or poorly controlled cardiac arrhythmias, uncontrolled thrombotic or hemorrhagic disease, interstitial pneumonia or pulmonary fibrosis, or in the judgment of the treating physician. Patients with other serious medical conditions that are not controlled.
7. Patients with ongoing or active psychiatric conditions or social situations that may limit adherence to treatment.
8. Patients with uncontrolled or poorly controlled hypertension (systolic \>160 mmHg or diastolic \>100 mmHg for \>4 weeks) despite standard medical care.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
19 Years
Study:
NCT04656002
Study Brief:
Protocol Section:
NCT04656002