205
Participants
Start Date
November 1, 2011
Primary Completion Date
May 16, 2014
Study Completion Date
March 31, 2016
Sorafenib (Nexavar, BAY43-9006)
Patients scheduled for treatment with sorafenib given in regular daily dose i.e. 800mg (400mg bid)
Many Locations
Lead Sponsor
Bayer
INDUSTRY