33
Participants
Start Date
July 31, 2006
Primary Completion Date
September 30, 2011
Study Completion Date
October 31, 2011
Nexavar (Sorafenib, BAY43-9006)
Sorafenib 200 mg orally BID interrupted dosing
Nexavar (Sorafenib, BAY43-9006)
Sorafenib 400 mg orally BID interrupted dosing
Bevacizumab
Bevacizumab 2.5 mg/kg intravenously
Bevacizumab
Bevacizumab 5 mg/kg intravenously
Bevacizumab
Bevacizumab 7.5 mg/kg intravenously
Bevacizumab
Bevacizumab 10 mg/kg intravenously
Paclitaxel
Paclitaxel 200 mg/m² intravenously
Carboplatin
Carboplatin AUC 6 intravenously
Rochester
Houston
Lead Sponsor
Bayer
INDUSTRY