Primary objective: Comparison of independently assessed progression free survival (PFS) in subjects administered Bevacizumab + Temsirolimus vs. those administered Bevacizumab + Interferon-Alfa. Secondary objectives: safety, Investigator assessed PFS, objective response rate (independently assessed), and overall survival.
Bevacizumab 10 mg/kg intravenous (IV) q8wks
Temsirolimus 25 mg IV weekly
Bevacizumab 10 mg/kg intravenous (IV) q8wks
Interferon-Alfa 9MU SC TIW
Rosario, Santa Fe Province, Argentina
Santa Fe, Santa Fe Province, Argentina
San Miguel de Tucumán, Tucumán Province, Argentina