Eligibility Module

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: 2025-12-24 @ 4:40 PM
Ignite Modification Date: 2025-12-24 @ 4:40 PM
NCT ID: NCT03430466
Eligibility Criteria: Inclusion Criteria: 1. Patients aged \>= 20 years at informed consent. 2. Patients who have provided written informed consent themselves. 3. Patients who have metastatic and/or advanced lesion 4. Documentation of ER-positive and/or PR-positive tumor (\>=1% positive stained cells). 5. Patients with cancer confirmed to be HER2-negative. 6. Patients with confirmed menopause 7. Patients who have plans of 2nd hormone therapy. 8. Patients with a measurable lesion based on RECIST 1.1 9. Patients with ECOG PS of 0 to 1. 10. Patients without any severe disorder in the major organs. Exclusion Criteria: \- Exclusion Criteria: 1. Active or prior documented autoimmune disease within the past 2 years. 2. Current or prior use of immunosuppressive medication within 28 days before the first dose of durvalumab or tremelimumab 3. Patients with central nervous system metastasis 4. Patients with life-threatening disease. 5. Patients with a history of treatment with anti-PD-1, anti-PD-L1, anti-PD-L2 or anti-CTLA-4 antibody drug. 6. Patients who have received live vaccination within 30 days before start of the investigational products. 7. Patients with a past medical history of pneumonia requiring steroid treatment or with a past medical history of interstitial pneumonia. 8. Patients considered ineligible for participation in this study by their attending physicians.
Healthy Volunteers: False
Sex: FEMALE
Minimum Age: 20 Years
Study: NCT03430466
Study Brief:
Protocol Section: NCT03430466