drugset / Trial / NCT01204177

Assessing BAY86-9766 Plus Sorafenib for the Treatment of Liver Cancer.

NCT01204177

Phase 2 Completed 70 enrolled Bayer
NaSingle-groupOpen-labelTreatment

Summary

This study investigates the safety and efficacy of the combination therapy with BAY86-9766 and sorafenib in patients with liver cancer. Safety will be determined by laboratory and other evaluations. Efficacy of the combination BAY86-9766 and sorafenib will be determined by disease control rate, overall survival, time to progression, response rate and duration of response.

Timeline

Start
2010-12
Primary completion
2011-08
Completion
2013-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Refametinib Small molecule 50 mg Oral
Subject Sorafenib Small molecule 800 mg