Summary
This is a multi-center, open-label, Phase 1, first-in-human (FIH), dose-escalation, and
dose expansion study to evaluate the safety, tolerability, pharmacokinetics (PK),
pharmacodynamics (PD), and efficacy of SRK-181 administered alone and in combination with
anti-PD-(L)1 therapy in adult patients with locally advanced or metastatic solid tumors.
The study is divided into 3 treatment parts (Part A1, Part A2, and Part B) and a
Long-Term Extension Phase (LTEP).