NCT04973163 is assessing BI 1823911 monotherapy and is designed to evaluate combinations with other anticancer therapies in pts with locally advanced/metastatic solid tumours with a KRAS G12C mutation….During early dose escalation (≥100 mg), 11 pts had disease control, including 8 with stable disease and 3 with confirmed PR (600 mg, n=2, lung and unknown cancer, Day 53 and 55; 900 mg, n=1, small intestine, Day 50).