drugset / Trial / NCT04527991

Study of Sacituzumab Govitecan Versus Physician's Choice of Treatment in Participants With Urothelial Cancer That Cannot Be Removed or Has Spread

NCT04527991 ↗

Phase 3 Completed 711 enrolled Gilead Sciences
RandomizedParallel-groupOpen-labelTreatment

Summary

The primary objective of this study is to assess overall survival (OS) with sacituzumab govitecan-hziy in comparison with treatment of physician's choice (TPC) in participants with metastatic or locally advanced unresectable urothelial cancer (UC).

Timeline

Start
2021-01-13
Primary completion
2025-07-04
Completion
2025-07-04

Outcome

Missed primary endpoint

registry analysis (superiority test); Sacituzumab Govitecan-hziy (SG) vs Treatment of Physician's Choice; p = 0.0870; Stratified Hazard Ratio 0.86 (95% CI 0.73 to 1.02); NCT04527991 ↗

paper Overall, participants who received sacituzumab govitecan did not live significantly longer than those who received chemotherapy. PMID 41277126 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Docetaxel Small molecule 75 mg/m2 Intravenous
Comparator Paclitaxel Small molecule 175 mg/m2 Intravenous
Subject Sacituzumab Govitecan Monoclonal antibody 10 mg/kg Intravenous
Comparator Vinflunine Small molecule 320 mg/m2 Intravenous

Indications