drugset / Trial / NCT05641545
IVAC-RCC-001: A Personalized Neoantigen Vaccine as Add-on to Standard of Care Checkpoint Inhibitor in Advanced/Metastatic RCC Patients
NaSingle-groupOpen-labelOther
Summary
This is a monocenter, single-arm, prospective phase Ib trial, designed to evaluate the safety, clinical toxicity and in vivo immunological effects of a patient-individualized peptide vaccination added to standard of care checkpoint blockade (nivolumab) in adult patients with metastatic/advanced renal cell carcinoma who experienced at least stable disease after four cycles of standard of care immune therapy (ipilimumab/nivolumab).
Timeline
- Start
- 2022-10-17
- Primary completion
- 2024-09-15
- Completion
- 2024-09-15
Outcome
Outcome not reported
Stopped (Enrollment): “Premature discontinuation due to üoor participant recruitment”
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | IVAC | Vaccine | — | Intramuscular |