Summary
This study will have two phases: a sacituzumab tirumotecan safety run-in and a Phase 3
portion. The safety run-in phase will be used to evaluate the efficacy and safety of
sacituzumab tirumotecan at the dose for evaluation in the Phase 3 portion. The purpose of
this study is to compare the efficacy and safety of sacituzumab tirumotecan versus
treatment of physician's choice as second-line treatment for participants with recurrent
or metastatic cervical cancer in the Phase 3 portion.
The primary study hypotheses are that, in the Phase 3 portion, sacituzumab tirumotecan
results in a superior overall survival compared to TPC in participants with high
trophoblast cell surface antigen 2 (TROP2) expression level and in all participants.