drugset / Trial / NCT01033240

CS1008- in Combination With Sorafenib Compared to Sorafenib Alone in Subjects With Advanced Liver Cancer

NCT01033240

Phase 2 Completed 172 enrolled Daiichi Sankyo
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to determine the safety and efficacy of CS-1008 in combination with sorafenib to sorafenib alone for treating liver cancer. Approximately 160 participants will take part in this study at approximately 22 sites (4 in the US, 8 in Japan, and 10 in Asia).

Timeline

Start
2010-07-09
Primary completion
2012-07-13
Completion
2013-09-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Sorafenib Small molecule 400 mg Oral
Subject tigatuzumab Monoclonal antibody 2 mg/kg Intravenous
Subject tigatuzumab Monoclonal antibody 4 mg/kg Intravenous
Subject tigatuzumab Monoclonal antibody 6 mg/kg Intravenous