The purpose of the study is to investigate the safety, tolerability, and preliminary anti-neoplastic activity of S095029 alone and in combination with Sym021 in patients with advanced solid tumor malignancies followed by an expansion phase of triple combinations. \*The study sponsor has made the decision not to move forward to the expansion part of the study due to strategic considerations, unrelated to any safety issues or concerns. The study will be stopped after completion of dose escalation parts 1a and 1b of the study.
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Adverse Events (AEs) (Dose escalation part)
Timeframe: Through study completion, up to 2 years
Incidence of dose limiting toxicities (DLTs) (Dose escalation part)
Timeframe: At the end of Cycle 1 (each cycle is 28 days)