Safety of AMG 706 Plus Panitumumab Plus Gemcitabine-Cisplatin in the Treatment of Patients With Advanced Cancer

PHASE1TerminatedINTERVENTIONAL
Enrollment

41

Participants

Timeline

Start Date

December 31, 2004

Primary Completion Date

June 30, 2007

Study Completion Date

April 30, 2008

Conditions
Lung CancerPancreatic CancerEsophageal Cancer
Interventions
DRUG

AMG 706

AMG 706 will be provided as 25-mg and 100-mg tablets and will be continuously self-administered orally once or twice daily based on cohort assignment starting on day 1 of Cycle 1.

BIOLOGICAL

Panitumumab

Panitumumab will be administered by intravenous (IV) infusion at a dose of 9 mg/kg on Day 1 of each 3-week cycle.

DRUG

Gemcitabine

Gemcitabine will be administered intravenously on Day 1 and Day 8 of each 21-day cycle at a dose of 1250 mg/m\^2.

DRUG

Cisplatin

Cisplatin will be administered intravenously on Day 1 of each 3-week cycle at a dose of 75 mg/m\^2.

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Amgen

INDUSTRY