This study investigates advanced solid tumors with a KRAS G12D mutation. It will explore how the investigational medication affects these tumors.
The study focuses on evaluating the safety, tolerability, and preliminary effectiveness of the investigational medication in people with this specific mutation.
- Who can participate: Adults with advanced solid tumors and a KRAS G12D mutation who have tried or cannot tolerate standard treatments may participate. Participants must have an ECOG performance score of 0 or 1.
- Study details: Participants will take an investigational medication orally. The study will assess how the body processes the medication and its effects on the tumor. An inactive substance that looks like the investigational medication but does not contain any medicine may be used for comparison.