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 @ 2:50 AM
Ignite Modification Date:
2025-12-25 @ 2:50 AM
NCT ID:
NCT04237233
Eligibility Criteria:
Inclusion Criteria:
Patients must be able to understand and voluntarily sign the informed consent form (ICF).
Patients must provide reliable contact information, including home phone numbers or follow-up phone number, and be voluntary to be followed up.
Patients must have agreed to use Tyvyt® to treat the target indication.
Exclusion Criteria:
Patients refuse to be included in the study or refuse to cooperate.
Patients have participated in another interventional studies within 4 weeks prior to enrollment.
Healthy Volunteers:
False
Sex:
ALL
Study:
NCT04237233
Study Brief:
Protocol Section:
NCT04237233