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 @ 6:30 PM
Ignite Modification Date:
2025-12-24 @ 6:30 PM
NCT ID:
NCT05522868
Eligibility Criteria:
Inclusion Criteria:
* A patient with a histologically or cytologically confirmed diagnosis of locally advanced or metastatic solid tumors.
* A person who has failed the known standard of care or has developed resistance to the standard of care and no longer has applicable standard of care
* A patient with at least one measurable lesion according to the RECIST v1.1 criteria.
* A person with Eastern Cooperative Oncology Group (ECOG) Performance status of 0 or 1.
* Those with an expected survival period of 3 months or more at the discretion of of the investigator.
Exclusion Criteria:
* A patient who has received drugs targeting High Mobility Group Box 1 (HMGB1).
* A patient who has received or is undergoing chemotherapy (including chemotherapy, radiation therapy, immunotherapy, hormone therapy, targeted therapy, biological products, and tumor embolization) within 28 days from the first administration date of the investigational drug.
* A person who needs to take contraindicated drugs or is expected to take them during the study period.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
19 Years
Study:
NCT05522868
Study Brief:
Protocol Section:
NCT05522868