302
Participants
Start Date
May 30, 2013
Primary Completion Date
August 6, 2016
Study Completion Date
December 29, 2016
Sorafenib (Nexavar, BAY43-9006)
sorafenib treatment (including dose, duration, modification) and TACE procedure are decided by the investigator
Multiple Locations
Lead Sponsor
Bayer
INDUSTRY