drugset / Trial / NCT02574455

Trial of Sacituzumab Govitecan in Participants With Refractory/Relapsed Metastatic Triple-Negative Breast Cancer (TNBC)

NCT02574455

Phase 3 Completed 529 enrolled Gilead Sciences
RandomizedParallel-groupOpen-labelTreatment

Summary

The primary objective of this study is to compare the efficacy of sacituzumab govitecan to the treatment of physician's choice (TPC) as measured by independently-reviewed Independent Review Committee (IRC) progression-free survival (PFS) in participants with locally advanced or metastatic triple-negative breast cancer (TNBC) previously treated with at least two systemic chemotherapy regimens for unresectable, locally advanced or metastatic disease, and without brain metastasis at baseline.

Timeline

Start
2017-11-07
Primary completion
2020-03-30
Completion
2020-12-08

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Capecitabine Small molecule 1000 mg/m2 Oral
Comparator Capecitabine Small molecule 1250 mg/m2 Oral
Comparator Eribulin Small molecule 0.67 mg/m2 Intravenous
Comparator Eribulin Small molecule 0.7 mg/m2 Intravenous
Comparator Eribulin Small molecule 1.23 mg/m2 Intravenous
Comparator Eribulin Small molecule 1.4 mg/m2 Intravenous
Comparator Gemcitabine Small molecule 800 mg/m2 Intravenous
Comparator Gemcitabine Small molecule 1200 mg/m2 Intravenous
Subject Sacituzumab Govitecan Monoclonal antibody 10 mg/kg Intravenous
Comparator Vinorelbine Small molecule 25 mg/m2 Intravenous

Indications