Oncogenic KRAS mutations are among the most prevalent driver events in solid tumors, with the KRAS G12D variant constituting the dominant allele in pancreatic ductal adenocarcinoma (PDAC) and a frequent alteration in non-small-cell lung cancer (NSCLC). Researchers from Ranok Therapeutics (Hangzhou) Co. Ltd. and collaborators described the preclinical profile of RNK-08954, an oral KRAS G12D inhibitor, in both in vitro and in vivo models.