This study investigates the treatment of refractory solid tumors.
The study evaluates the safety and dosage of an investigational medication to determine the best dose for future studies. It also looks at how the medication is absorbed and its preliminary effectiveness.
- Who can participate: Adults aged 18 and older with solid tumors that have not responded to standard treatments or who refuse standard treatments are eligible. Participants must have a performance status of 2 or less.
- Study details: Participants will take the investigational medication orally twice daily. The study will also test the medication in combination with a TKI for certain patients.