drugset / Trial / NCT01033240
CS1008- in Combination With Sorafenib Compared to Sorafenib Alone in Subjects With Advanced Liver Cancer
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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 |