drugset / Trial / NCT05280457
HPV 16-positive and/or HPV 18-positive Recurrent and/or For Patients With Metastatic Head and Neck Cancer to Evaluate GX-188E DNA Vaccination, GX-I7 and Nivolumab Combination Therapy
NaSingle-groupOpen-labelTreatment
Summary
This study is to explore the efficacy and safety of GX-188E DNA vaccination, GX-I7, and nivolumab combination therapy in HPV 16-positive and/or HPV-18 positive R/M HNSCC patients. The objective of this study is as follows. * Primary objective: Objective response rate (ORR) according to RECIST v1.1 * Secondary objectives: disease control rate (DCR) according to RECIST v1.1, progression-free survival (PFS) at 6 months, median progression-free survival (PFS), median overall survival (OS), biomarker correlation, safety and tolerability.
Timeline
- Start
- 2022-04-15
- Primary completion
- 2027-01
- Completion
- 2027-01
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | GX-188E | Vaccine | 2 mg | Intramuscular |
| Subject | NT-I7 | Protein / enzyme biologic | 960 ug/kg | — |
| Subject | NT-I7 | Protein / enzyme biologic | 1200 ug/kg | — |
| Subject | Nivolumab | Monoclonal antibody | 3 mg/kg | Intravenous |