drugset / Trial / NCT01631552

Study of Sacituzumab Govitecan-hziy (IMMU-132) in Adults With Epithelial Cancer

NCT01631552

Phase 1/2 Completed 515 enrolled Gilead Sciences
Non-randomizedSequentialOpen-labelTreatment

Summary

The primary objective in Phase I is to evaluate the safety and tolerability of sacituzumab govitecan-hziy (SG) as a single agent administered in 21-day treatment cycles in previously treated participants with advanced epithelial cancer. In Phase II, the primary objective is to evaluate the safety and efficacy of sacituzumab govitecan-hziy administered in 21-day treatment cycles at a dose selected in Phase I. Tumor types in the study will include: cervical, colorectal, endometrial, ovarian, esophageal, gastric adenocarcinoma, glioblastoma multiforme, head and neck cancers- squamous cell, hepatocellular, prostate, non-small-cell lung cancer, pancreatic, renal cell, small-cell lung cancer, non-triple negative breast cancer (non-TNBC), triple-negative breast cancer (TNBC) and metastatic urothelial cancer (mUC).

Timeline

Start
2012-12-17
Primary completion
2019-03-01
Completion
2020-08-13

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Sacituzumab Govitecan Monoclonal antibody 8 mg/kg Intravenous
Subject Sacituzumab Govitecan Monoclonal antibody 10 mg/kg Intravenous
Subject Sacituzumab Govitecan Monoclonal antibody 12 mg/kg Intravenous
Subject Sacituzumab Govitecan Monoclonal antibody 18 mg/kg Intravenous