Sone-296 ((exclusive)) Jun 2026

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| Parameter | Details | |-----------|---------| | | Open‑label, dose‑escalation (3 + 3), followed by expansion cohorts. | | Population | Adults with advanced solid tumors refractory to standard therapy. | | Dose range | 5 mg – 200 mg QD oral. | | Primary endpoints | Safety/tolerability, MTD, pharmacokinetics. | | Key secondary endpoints | Preliminary efficacy (RECIST response), pharmacodynamics (target inhibition in tumor biopsies). | | Status | Completed (2024); MTD = 150 mg QD, RP2D = 120 mg QD. |

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