Table 2.
ClinicalTrials.gov Trial ID | Intervention | Primary end point | Study status | Study design |
---|---|---|---|---|
NCT03811002 | CRT (EP) ± concurrent atezolizumab | PFS, OS | Active, Recruiting | Phase II/III |
NCT02402920 | CRT (EP) + concurrent pembrolizumab | Pembrolizumab maximum tolerated dose | Active, Recruiting | Phase I |
NCT04189094 | CRT (EP) ± concurrent sintilimab | PFS at 2 years | Active, not yet recruiting | Phase II |
NCT03540420 (ACHILES) | CRT (EP) ± post-treatment atezolizumab | OS at 2 years | Active, Recruiting | Phase II |
NCT03585998 | CRT (EP) + concurrent and consolidation durvalumab | PFS | Active, Recruiting | Phase II |
NCT03703297 (ADRIATIC) | Post-CRT (EP) durvalumab vs. durvalumab + tremelimumab vs. placebo | PFS, OS | Active, Recruiting | Phase III |
CRT, chemoradiotherapy; EP, etoposide-cisplatin; PFS, progression-free survival; OS, overall survival.