Overview
A Single-center Clinical Study to Evaluate the Safety and Efficacy of Autologous Bone Marrow-derived DCs(CellgramDC-WT1) and Immune Checkpoint Inhibitors in Patients With Metastatic Pancreatic Cancer Who Have Failed First-line or More Standard Chemo
Status:
Not yet recruiting
Not yet recruiting
Trial end date:
2025-12-31
2025-12-31
Target enrollment:
0
0
Participant gender:
All
All
Summary
To evaluate the safety and effectiveness of immune cell therapy using autologous bone marrow-derived dendritic cells and immune checkpoint inhibitors in patients with metastatic pancreatic cancer who have failed at least one standard anticancer treatment.Phase:
Phase 1/Phase 2Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Soonchunhyang University Hospital
Criteria
Inclusion Criteria:- Patients histologically confirmed to have pancreatic cancer and diagnosed as recurrent
or metastatic
- Patients whose disease was confirmed to have progressed according to RECIST v1.1 after
1st or more standard anticancer treatments
- Patients satisfying systemic performance status ECOG 0-2
- Patients who have not undergone surgery, radiation therapy, or immunotherapy within 4
weeks and have recovered from side effects (However, tissue collection procedures that
do not affect the test subject's condition are permitted at the discretion of the
researcher.)
- Patients who voluntarily agreed in writing to participate in this clinical study
Exclusion Criteria:
- Patients with malignant tumors other than non-melanoma skin cancer in the past 3 years
- Patients who have previously received anti-tumor immunotherapy (anti-PD1, anti-PDL-1,
or CTLA4 inhibitor, etc.) or participated in clinical studies related to immunotherapy
or cell therapy
- Patients with active autoimmune disease requiring systemic immunosuppressive treatment
- Patients with a history of organ or hematopoietic stem cell transplantation
- Patients with acute or chronic infection requiring systemic treatment
- Other cases where the test manager determines that it is not suitable for clinical
research