85
Participants
Start Date
May 28, 2009
Primary Completion Date
August 8, 2011
Study Completion Date
June 25, 2019
Sunitinib
Sunitinib will be administered 50 mg QD and is considered to be the background therapy as it is licensed for treatment of reneal cell cancer (RCC) and will be administered to all participants.
Trebananib
Administered until a participant develops disease progression, clinical progression, unacceptable toxicity, withdraws consent, or death.
Lead Sponsor
Amgen
INDUSTRY