47
Participants
Start Date
November 30, 2005
Primary Completion Date
September 30, 2014
Study Completion Date
September 30, 2014
Erlotinib
Erlotinib (150 mg PO QD) plus sulindac (150 mg PO BID) (Arm A), Erlotinib (150 mg PO QD) (Arm B) or placebo (for Erlotinib) QD (Arm C).
Erlotinib plus sulindac
Erlotinib (150 mg PO QD) plus sulindac (150 mg PO BID) (Arm A), Erlotinib (150 mg PO QD) (Arm B) or placebo (for Erlotinib) QD (Arm C).
Placebo
Erlotinib (150 mg PO QD) plus sulindac (150 mg PO BID) (Arm A), Erlotinib (150 mg PO QD) (Arm B) or placebo (for Erlotinib) QD (Arm C).
University of Pittsburgh Cancer Institute, Pittsburgh
Collaborators (1)
OSI Pharmaceuticals
INDUSTRY
University of Pittsburgh
OTHER