Clinical Trial | Phase | Target | Study Group | Control Group | Stage | Primary Outcome |
S1914/NRG | III | 480 | Atezolizumab + SBRT | SBRT | I-IIA and limited T3 | OS |
NRG-LU004 (ARCHON-1) | I | 24 | Accelerated/Conventional RT + Durvalumab | none | II-III | Safety |
NCT03833154 (PACIFIC-4) | III | 733 | Durvalumab + SBRT | SBRT/Placebo | II-III | PFS |
NCT03924869 | III | 530 | Pembrolizumab + SBRT | SBRT/Placebo | I-II | EFS/OS |
NCT03383302 | I/II | 31 | Nivolumab + SBRT | SBRT/Placebo | I-II | Safety |
NCT03217071 | I-II | 12 | Pembrolizumab + SBRT (single dose)-surgery | Pembrolizumab-surgery | I-IIIA | change in tumor infiltrating CD3 + T cells |
NCT03237377 | II | 9 | Durvalumab + tremelimumab/RT | Durvalumab/RT | IIIA | Safety |