In this Phase 2, Single-Arm, Multi-Center, Open-Label Study, participants with previously treated locally advanced unresectable or metastatic solid tumors with mismatched repair deficient (dMMR) or microsatellite instability-high (MSI-H) will be treated with anti-PD-1 Monoclonal Antibody Tislelizumab (BGB-A317).
Protocol Amendment History
18 amendments
This ClinicalTrials.gov record has been amended 18 times since 2018-11-08; most recent amendment 2026-07-09.