drugset / Trial / NCT05767684
Neoantigen Derived DCs as Cancer Treatment
Phase 1
Unknown
12 enrolled
National Health Research Institutes, Taiwan
National Cheng-Kung University Hospital · collab
RandomizedParallel-groupOpen-labelTreatment
Summary
Tumor lysate or carcinoembryonic antigen (CEA) derived DCs-based therapy is safe and can elicites remarkable T-cell responses but mostly did not really transfer into significant clinical benefit. One possible reason is the lack of effective antigen and the immunosuppressive microenvironment. Now we are exploring another new strategy, prediction of neoantigen for priming DCs as cell-based therapy with or without booster of anti-VEGF/anti-PD-1.
Timeline
- Start
- 2023-06-01
- Primary completion
- 2025-03-30
- Completion
- 2026-03-30
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | DC vaccine | Vaccine | 1.5e+06 cells | Subcutaneous |
| Subject | Lenvatinib | Small molecule | 10 mg | — |
| Subject | Nivolumab | Monoclonal antibody | 3 mg/kg | — |