The primary objective of this trial is to estimate efficacy of the novel regimen. The primary endpoint is the 1-year PFS rate after treatment with one dose of pembrolizumab followed by four to six cycles of chemo-immunotherapy with P-BrECADD, and PET-guided radiotherapy as per standard of care
Protocol Amendment History
2 amendments
This ClinicalTrials.gov record has been amended 2 times since 2023-09-19; most recent amendment 2025-04-02.