Overview

Neoantigen DNA Vaccine in Combination With Nivolumab/Ipilimumab and PROSTVAC in Metastatic Hormone-Sensitive Prostate Cancer

Status:
Active, not recruiting
Trial end date:
2024-01-10
Target enrollment:
Participant gender:
Summary
This study study aims to elucidate the immune responses to a shared antigen vaccine (PROSTVAC) and tumor specific antigens generated DNA vaccine in combination with checkpoint blockade using nivolumab (anti-PD-1), and ipilimumab (anti-CTLA-4). Additionally, the investigators will study the impact of the combination immunotherapy on peripheral T cell activation, as well as immune response in the tumor microenvironment. Finally, the investigators will evaluate the safety and tolerability to this novel personalized immunotherapy in combination with checkpoint blockade.
Phase:
Phase 1
Details
Lead Sponsor:
Washington University School of Medicine
Collaborators:
Bavarian Nordic
Bristol-Myers Squibb
Prostate Cancer Foundation
The Foundation for Barnes-Jewish Hospital
Treatments:
Antibodies, Monoclonal
Hormones
Ipilimumab
Nivolumab
Vaccines