31
Participants
Start Date
January 21, 2010
Primary Completion Date
March 21, 2014
Study Completion Date
February 13, 2015
MET/VEGFR2 inhibitor Foretinib
"PhaseI and Phase II Arm A:~Foretinib PO daily dosing starting cycle 1 day 15 and erlotinib PO daily dosing starting cycle 1 day 1. Recommended Phase II dose to be determine in Phase I."
erlotinib hydrochloride
erlotinib PO daily dosing starting cycle 1 day 1. Recommended Phase II dose to be determine in Phase I.
laboratory biomarker analysis
Tumour markers alone cannot be used to assess objective tumour response. If markers are initially above the upper normal limit, however, they must normalize for a patient to be considered in complete response
BCCA - Vancouver Cancer Centre, Vancouver
Juravinski Cancer Centre at Hamilton Health Sciences, Hamilton
Ottawa Health Research Institute - General Division, Ottawa
Univ. Health Network-Princess Margaret Hospital, Toronto
Lead Sponsor
Collaborators (1)
GlaxoSmithKline
INDUSTRY
NCIC Clinical Trials Group
NETWORK