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Clinical Trial 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.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03532217
Study type Interventional
Source Washington University School of Medicine
Contact
Status Completed
Phase Phase 1
Start date September 14, 2018
Completion date July 25, 2022

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