MET/VEGFR2 Inhibitor GSK1363089 and Erlotinib Hydrochloride or Erlotinib Hydrochloride Alone in Locally Advanced or Metastatic NSCLC That Has Not Responded to Previous Chemotherapy

PHASE1/PHASE2CompletedINTERVENTIONAL
Enrollment

31

Participants

Timeline

Start Date

January 21, 2010

Primary Completion Date

March 21, 2014

Study Completion Date

February 13, 2015

Conditions
Lung Cancer
Interventions
DRUG

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."

DRUG

erlotinib hydrochloride

erlotinib PO daily dosing starting cycle 1 day 1. Recommended Phase II dose to be determine in Phase I.

OTHER

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

Trial Locations (4)

V5Z 4E6

BCCA - Vancouver Cancer Centre, Vancouver

L8V 5C2

Juravinski Cancer Centre at Hamilton Health Sciences, Hamilton

K1H 8L6

Ottawa Health Research Institute - General Division, Ottawa

M5G 2M9

Univ. Health Network-Princess Margaret Hospital, Toronto

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

GlaxoSmithKline

INDUSTRY

lead

NCIC Clinical Trials Group

NETWORK