Safety of AMG 706 Plus Panitumumab Plus Chemotherapy in the Treatment of Subjects With Metastatic Colorectal Cancer

Sponsor

Amgen (Industry)

Overall Status

Completed

CT.gov ID

NCT00101894

Collaborator

(none)

119

Enrollment

Arms

Duration (Months)

Study Details

Study Description

Brief Summary

The purpose of this study is to characterize the safety and tolerability of AMG 706 plus panitumumab when administered with either FOLFIRI or FOLFOX4 chemotherapy regimens. This is a Phase 1b clinical study.

Condition or Disease	Intervention/Treatment	Phase
Rectal Cancer Colon Cancer	Drug: FOLFOX-4 Drug: AMG 706 Biological: Panitumumab (Part 1a only) Drug: FOLFIRI	Phase 1

Study Design

Study Type:

Interventional

Actual Enrollment :

119 participants

Allocation:

Non-Randomized

Intervention Model:

Parallel Assignment

Masking:

None (Open Label)

Primary Purpose:

Treatment

Official Title:

An Open-Label, Dose-Finding Study to Evaluate the Safety of AMG 706 Plus Panitumumab Plus Chemotherapy in the Treatment of Subjects With Metastatic Colorectal Cancer

Study Start Date :

Dec 1, 2004

Actual Primary Completion Date :

Apr 1, 2010

Actual Study Completion Date :

Dec 1, 2011

Arms and Interventions

Arm	Intervention/Treatment
Experimental: Part 2 AMG 706 (MTD) + FOLFOX-4 Maximum Tolerated Dose of AMG 706 established in Part 1b + FOLFOX-4	Drug: FOLFOX-4 The FOLFOX-4 regimen will be administered every 2 weeks as follows: Day 1: oxaliplatin (ELOXATIN™) 85 mg/m2 IV infusion and leucovorin racemate 200 mg/m2 (or 100 mg/m2 l-LV) IV infusion given over 120 ± 10 minutes at the same time in separate bags using a Y-line, followed by 5-FU 400 mg/m2 IV bolus given over 2 to 4 minutes, followed by 5-FU 600 mg/m2 IV infusion as a 22-hour ± 2 hours continuous infusion Day 2: leucovorin racemate 200 mg/m2 (or 100 mg/m2 l-LV) IV infusion over 120 ± 10 minutes, followed by 5-FU 400 mg/m2 IV bolus given over 2 to 4 minutes, followed Drug: AMG 706 AMG 706 is a small organic molecule that has been shown in preclinical pharmacology studies to be a potent, oral, multi-kinase inhibitor with anti-angiogenic and anti-tumor activity achieved by selectively inhibiting all known VEGF receptors, PDGF receptor, and Kit.
Experimental: 125 mg QD AMG 706 + FOLFOX-4 125 mg QD AMG 706 + FOLFOX-4	Drug: FOLFOX-4 The FOLFOX-4 regimen will be administered every 2 weeks as follows: Day 1: oxaliplatin (ELOXATIN™) 85 mg/m2 IV infusion and leucovorin racemate 200 mg/m2 (or 100 mg/m2 l-LV) IV infusion given over 120 ± 10 minutes at the same time in separate bags using a Y-line, followed by 5-FU 400 mg/m2 IV bolus given over 2 to 4 minutes, followed by 5-FU 600 mg/m2 IV infusion as a 22-hour ± 2 hours continuous infusion Day 2: leucovorin racemate 200 mg/m2 (or 100 mg/m2 l-LV) IV infusion over 120 ± 10 minutes, followed by 5-FU 400 mg/m2 IV bolus given over 2 to 4 minutes, followed Drug: AMG 706 AMG 706 is a small organic molecule that has been shown in preclinical pharmacology studies to be a potent, oral, multi-kinase inhibitor with anti-angiogenic and anti-tumor activity achieved by selectively inhibiting all known VEGF receptors, PDGF receptor, and Kit.
Experimental: 50 mg QD AMG706 + panitumumab + FOLFIRI 50 mg QD AMG706 + panitumumab + FOLFIRI	Drug: AMG 706 AMG 706 is a small organic molecule that has been shown in preclinical pharmacology studies to be a potent, oral, multi-kinase inhibitor with anti-angiogenic and anti-tumor activity achieved by selectively inhibiting all known VEGF receptors, PDGF receptor, and Kit. Biological: Panitumumab (Part 1a only) Panitumumab will be administered by IV infusion at a dose of 6 mg/kg on day 1 of each 2-week cycle. Drug: FOLFIRI Irinotecan will be administered over 90 minutes ± 15 minutes on day 1 of each 2-week cycle. Leucovorin will be administered over 2 hours ± 15 minutes during the irinotecan infusion but without mixing, immediately followed by a 5-FU bolus and a 5-FU 46-hour ± 2-hour continuous intravenous infusion.
Experimental: Part 2 AMG 706 (MTD) + FOLFIRI Maximum Tolerated Dose of AMG 706 established in Part 1b + FOLFIRI	Drug: AMG 706 AMG 706 is a small organic molecule that has been shown in preclinical pharmacology studies to be a potent, oral, multi-kinase inhibitor with anti-angiogenic and anti-tumor activity achieved by selectively inhibiting all known VEGF receptors, PDGF receptor, and Kit. Drug: FOLFIRI Irinotecan will be administered over 90 minutes ± 15 minutes on day 1 of each 2-week cycle. Leucovorin will be administered over 2 hours ± 15 minutes during the irinotecan infusion but without mixing, immediately followed by a 5-FU bolus and a 5-FU 46-hour ± 2-hour continuous intravenous infusion.
Experimental: 100 mg QD AMG 706 + FOLFIRI 100 mg AMG 706 + FOLFIRI	Drug: AMG 706 AMG 706 is a small organic molecule that has been shown in preclinical pharmacology studies to be a potent, oral, multi-kinase inhibitor with anti-angiogenic and anti-tumor activity achieved by selectively inhibiting all known VEGF receptors, PDGF receptor, and Kit. Drug: FOLFIRI Irinotecan will be administered over 90 minutes ± 15 minutes on day 1 of each 2-week cycle. Leucovorin will be administered over 2 hours ± 15 minutes during the irinotecan infusion but without mixing, immediately followed by a 5-FU bolus and a 5-FU 46-hour ± 2-hour continuous intravenous infusion.
Experimental: 75 mg QD AMG 706 + panitumumab + FOLFOX-4 75 mg QD AMG 706 + panitumumab + FOLFOX-4	Drug: FOLFOX-4 The FOLFOX-4 regimen will be administered every 2 weeks as follows: Day 1: oxaliplatin (ELOXATIN™) 85 mg/m2 IV infusion and leucovorin racemate 200 mg/m2 (or 100 mg/m2 l-LV) IV infusion given over 120 ± 10 minutes at the same time in separate bags using a Y-line, followed by 5-FU 400 mg/m2 IV bolus given over 2 to 4 minutes, followed by 5-FU 600 mg/m2 IV infusion as a 22-hour ± 2 hours continuous infusion Day 2: leucovorin racemate 200 mg/m2 (or 100 mg/m2 l-LV) IV infusion over 120 ± 10 minutes, followed by 5-FU 400 mg/m2 IV bolus given over 2 to 4 minutes, followed Drug: AMG 706 AMG 706 is a small organic molecule that has been shown in preclinical pharmacology studies to be a potent, oral, multi-kinase inhibitor with anti-angiogenic and anti-tumor activity achieved by selectively inhibiting all known VEGF receptors, PDGF receptor, and Kit. Biological: Panitumumab (Part 1a only) Panitumumab will be administered by IV infusion at a dose of 6 mg/kg on day 1 of each 2-week cycle.
Experimental: 75 mg BID AMG 706 + panitumumab + FOLFIRI 75 mg BID AMG 706 + panitumumab + FOLFIRI	Drug: AMG 706 AMG 706 is a small organic molecule that has been shown in preclinical pharmacology studies to be a potent, oral, multi-kinase inhibitor with anti-angiogenic and anti-tumor activity achieved by selectively inhibiting all known VEGF receptors, PDGF receptor, and Kit. Biological: Panitumumab (Part 1a only) Panitumumab will be administered by IV infusion at a dose of 6 mg/kg on day 1 of each 2-week cycle. Drug: FOLFIRI Irinotecan will be administered over 90 minutes ± 15 minutes on day 1 of each 2-week cycle. Leucovorin will be administered over 2 hours ± 15 minutes during the irinotecan infusion but without mixing, immediately followed by a 5-FU bolus and a 5-FU 46-hour ± 2-hour continuous intravenous infusion.
Experimental: 125 mg QD AMG 706 + panitumumab + FOLFIRI 125 mg QD AMG 706 + panitumumab + FOLFIRI	Drug: AMG 706 AMG 706 is a small organic molecule that has been shown in preclinical pharmacology studies to be a potent, oral, multi-kinase inhibitor with anti-angiogenic and anti-tumor activity achieved by selectively inhibiting all known VEGF receptors, PDGF receptor, and Kit. Biological: Panitumumab (Part 1a only) Panitumumab will be administered by IV infusion at a dose of 6 mg/kg on day 1 of each 2-week cycle. Drug: FOLFIRI Irinotecan will be administered over 90 minutes ± 15 minutes on day 1 of each 2-week cycle. Leucovorin will be administered over 2 hours ± 15 minutes during the irinotecan infusion but without mixing, immediately followed by a 5-FU bolus and a 5-FU 46-hour ± 2-hour continuous intravenous infusion.
Experimental: 125 mg QD AMG 706 + FOLFIRI 125 mg QD AMG 706 + FOLFIRI	Drug: AMG 706 AMG 706 is a small organic molecule that has been shown in preclinical pharmacology studies to be a potent, oral, multi-kinase inhibitor with anti-angiogenic and anti-tumor activity achieved by selectively inhibiting all known VEGF receptors, PDGF receptor, and Kit. Drug: FOLFIRI Irinotecan will be administered over 90 minutes ± 15 minutes on day 1 of each 2-week cycle. Leucovorin will be administered over 2 hours ± 15 minutes during the irinotecan infusion but without mixing, immediately followed by a 5-FU bolus and a 5-FU 46-hour ± 2-hour continuous intravenous infusion.
Experimental: 100 mg QD AMG 706 + panitumumab + FOLFIRI 100 mg QD AMG 706 + panitumumab + FOLFIRI	Drug: AMG 706 AMG 706 is a small organic molecule that has been shown in preclinical pharmacology studies to be a potent, oral, multi-kinase inhibitor with anti-angiogenic and anti-tumor activity achieved by selectively inhibiting all known VEGF receptors, PDGF receptor, and Kit. Biological: Panitumumab (Part 1a only) Panitumumab will be administered by IV infusion at a dose of 6 mg/kg on day 1 of each 2-week cycle. Drug: FOLFIRI Irinotecan will be administered over 90 minutes ± 15 minutes on day 1 of each 2-week cycle. Leucovorin will be administered over 2 hours ± 15 minutes during the irinotecan infusion but without mixing, immediately followed by a 5-FU bolus and a 5-FU 46-hour ± 2-hour continuous intravenous infusion.
Experimental: 75 mg QD AMG 706 + FOLFOX-4 75 mg QD AMG 706 + FOLFOX-4	Drug: FOLFOX-4 The FOLFOX-4 regimen will be administered every 2 weeks as follows: Day 1: oxaliplatin (ELOXATIN™) 85 mg/m2 IV infusion and leucovorin racemate 200 mg/m2 (or 100 mg/m2 l-LV) IV infusion given over 120 ± 10 minutes at the same time in separate bags using a Y-line, followed by 5-FU 400 mg/m2 IV bolus given over 2 to 4 minutes, followed by 5-FU 600 mg/m2 IV infusion as a 22-hour ± 2 hours continuous infusion Day 2: leucovorin racemate 200 mg/m2 (or 100 mg/m2 l-LV) IV infusion over 120 ± 10 minutes, followed by 5-FU 400 mg/m2 IV bolus given over 2 to 4 minutes, followed Drug: AMG 706 AMG 706 is a small organic molecule that has been shown in preclinical pharmacology studies to be a potent, oral, multi-kinase inhibitor with anti-angiogenic and anti-tumor activity achieved by selectively inhibiting all known VEGF receptors, PDGF receptor, and Kit.
Experimental: 100 mg QD AMG 706 + FOLFOX-4 100 mg QD AMG 706 + FOLFOX-4	Drug: FOLFOX-4 The FOLFOX-4 regimen will be administered every 2 weeks as follows: Day 1: oxaliplatin (ELOXATIN™) 85 mg/m2 IV infusion and leucovorin racemate 200 mg/m2 (or 100 mg/m2 l-LV) IV infusion given over 120 ± 10 minutes at the same time in separate bags using a Y-line, followed by 5-FU 400 mg/m2 IV bolus given over 2 to 4 minutes, followed by 5-FU 600 mg/m2 IV infusion as a 22-hour ± 2 hours continuous infusion Day 2: leucovorin racemate 200 mg/m2 (or 100 mg/m2 l-LV) IV infusion over 120 ± 10 minutes, followed by 5-FU 400 mg/m2 IV bolus given over 2 to 4 minutes, followed Drug: AMG 706 AMG 706 is a small organic molecule that has been shown in preclinical pharmacology studies to be a potent, oral, multi-kinase inhibitor with anti-angiogenic and anti-tumor activity achieved by selectively inhibiting all known VEGF receptors, PDGF receptor, and Kit.
Experimental: 50 mg QD AMG 706 + panitumumab + FOLFOX-4 50 mg QD AMG 706 + panitumumab + FOLFOX-4	Drug: FOLFOX-4 The FOLFOX-4 regimen will be administered every 2 weeks as follows: Day 1: oxaliplatin (ELOXATIN™) 85 mg/m2 IV infusion and leucovorin racemate 200 mg/m2 (or 100 mg/m2 l-LV) IV infusion given over 120 ± 10 minutes at the same time in separate bags using a Y-line, followed by 5-FU 400 mg/m2 IV bolus given over 2 to 4 minutes, followed by 5-FU 600 mg/m2 IV infusion as a 22-hour ± 2 hours continuous infusion Day 2: leucovorin racemate 200 mg/m2 (or 100 mg/m2 l-LV) IV infusion over 120 ± 10 minutes, followed by 5-FU 400 mg/m2 IV bolus given over 2 to 4 minutes, followed Drug: AMG 706 AMG 706 is a small organic molecule that has been shown in preclinical pharmacology studies to be a potent, oral, multi-kinase inhibitor with anti-angiogenic and anti-tumor activity achieved by selectively inhibiting all known VEGF receptors, PDGF receptor, and Kit. Biological: Panitumumab (Part 1a only) Panitumumab will be administered by IV infusion at a dose of 6 mg/kg on day 1 of each 2-week cycle.
Experimental: 75 mg QD AMG706 + panitumumab + FOLFIRI 75 mg QD AMG706 + panitumumab + FOLFIRI	Drug: AMG 706 AMG 706 is a small organic molecule that has been shown in preclinical pharmacology studies to be a potent, oral, multi-kinase inhibitor with anti-angiogenic and anti-tumor activity achieved by selectively inhibiting all known VEGF receptors, PDGF receptor, and Kit. Biological: Panitumumab (Part 1a only) Panitumumab will be administered by IV infusion at a dose of 6 mg/kg on day 1 of each 2-week cycle. Drug: FOLFIRI Irinotecan will be administered over 90 minutes ± 15 minutes on day 1 of each 2-week cycle. Leucovorin will be administered over 2 hours ± 15 minutes during the irinotecan infusion but without mixing, immediately followed by a 5-FU bolus and a 5-FU 46-hour ± 2-hour continuous intravenous infusion.

Outcome Measures

Primary Outcome Measures

Part 1a - The incidence of adverse events and clinical laboratory abnormalities defined as dose-limiting toxicities [First 2 cycles]
Part 1b - The incidence of adverse events and clinical laboratory abnormalities defined as dose-limiting toxicities [First 2 cycles]
Part 2 - The overall objective tumor response rate (complete and partial response) in subjects treated with AMG 706 (at the dose determined in Part 1b), with either the FOLFIRI or FOLFOX-4 chemotherapy regimen [Every 8 weeks (+/- 7 days)]

Secondary Outcome Measures

Part 1a - The PK of irinotecan (and its active metabolite SN38) when administered as a part of the FOLFIRI regimen with panitumumab and AMG 706 [Cycle 1 and 2 (Days 1, 2, 3)]
Part 1a - The PK of oxaliplatin when administered as a part of the FOLFOX-4 regimen with panitumumab and AMG 706 [Cycle 1 and 2 (Day 1)]
Part 1a - The objective tumor response rate (complete and partial response) throughout the study [Every 6 to 8 weeks]
Part 1b - The incidence of adverse events and clinical laboratory abnormalities not defined as dose-limiting toxicities [Every visit]
Part 1b - The PK of AMG 706 when administered with either the FOLFIRI or FOLFOX-4 chemotherapy regimen [Cycle 2 (Day 1-2), Cycle 3 (Day 1)]
Part 1b - The PK of 5-FU when administered as a part of the FOLFIRI or FOLFOX-4 regimen with AMG 706 [Cycle 1 and 2 (Day 3)]
Part 2 - Duration of response: (Calculated for only those subjects who respond) [Time from first objective tumor response (subsequently confirmed at least 4 weeks later) to objective disease progression or death.]
Part 2 - Time-to-progression [Time from first dose of investigational product to objective disease progression or death due to disease progression.]
Part 1b - The PK of irinotecan (and its active metabolite SN38) when administered as a part of the FOLFIRI regimen with AMG 706 [Cycle 1 and 2 (Days 1, 2, 3)]
Part 1b- The PK of oxaliplatin when administered as a part of the FOLFOX-4 regimen with AMG 706 [Cycle 1 and 2 (Day 1)]
Part 1b - The objective tumor response rate (complete and partial response) throughout the study [Every 8 weeks (+/- 7 days)]
Part 2 - Overall survival [Time from first dose of investigational product to death. Subjects who have not died while on study or are lost to follow-up will be censored at their last contact date. (Time on study plus 36 months of long term follow-up)]
Part 2 - The incidence of adverse events and clinical laboratory abnormalities [Every visit]
Part 2 - The PK of AMG 706 when administered with either the FOLFIRI or FOLFOX-4 chemotherapy regimen (at a subset of the study centers with the capabilities to draw, ship and process PK samples) [Cycles 2, 4, 7, and every 3 subsequent cycles (Day 1)]
Exploratory - Potential biomarker development based on assessment of blood cells, tumor cells, and urine and the proposed mechanism of action of study drugs, and response [Day 1 of cycles 1 and 2, and within 7 days of a radiographic assessment]
Exploratory - The effects of genetic variation in drug metabolism genes, cancer genes, and drug target genes on subject response to investigational products (separate informed consent) [Day 1 of cycles 1 and 2, and within 7 days of a radiographic assessment]
Part 2 - Progression-free survival time [Time from first dose of investigational product to objective disease progression or death, subjects who have not progressed or died while on study will be censored at their last evaluable assessment date.]
Part 2 - Incidence of subjects undergoing resection of metastases for curative intent [As needed]
Part 1a - The incidence of adverse events and clinical laboratory abnormalities not defined as dose-limiting toxicities [Every visit]
Part 1a - The PK of AMG 706 when administered with panitumumab and either the FOLFIRI or FOLFOX-4 chemotherapy regimen [Cycle 2 (Day 1-2), Cycle 3 (Day 1)]
Part 1a - The serum concentration of panitumumab when administered with AMG 706 and either the FOLFIRI or FOLFOX-4 chemotherapy regimen [Cycle 1 (Day 1), Cycle 2 (Day 1), Cycle 4 (Day 1)]
Part 1a - The incidence of HAPA response following panitumumab administration [Cycle 1 (Day 1), Cycle 4 (Day 1), End of Study]
Part 1a - The PK of 5-FU when administered as a part of the FOLFIRI or FOLFOX-4 regimen with panitumumab and AMG 706 [Cycle 1 and 2 (Day 3)]

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years and Older

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

For complete inclusion and exclusion criteria, please refer to the investigator. Inclusion Criteria

Competent to comprehend, sign, and date an Institutional Review Board (IRB) approved informed consent form
Diagnosis of metastatic colorectal adenocarcinoma (may have received 1 prior chemotherapy regimen for metastatic CRC)
Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
Adequate hematological function
Adequate renal function
Adequate hepatic function
Life expectancy of greater than or equal to 3 months as documented by the investigator

Exclusion Criteria:

More than 1 prior chemotherapy regimen for metastatic CRC
Central nervous system (CNS) metastases
History of venous thrombosis
Myocardial infarction, cerebrovascular accident, transient ischemic attack, grade 2 or greater peripheral vascular disease, congestive heart failure, ongoing arrhythmias requiring medication, or unstable angina within 1 year before study enrollment
History of interstitial pneumonitis or pulmonary fibrosis or evidence of interstitial pneumonitis or pulmonary fibrosis on screening chest computed tomograph (CT) scan
Average systolic blood pressure > 150mm Hg or average diastolic blood pressure of > 90mm Hg
Radiotherapy within 28 days of study enrollment or within 14 days of study enrollment for peripheral lesions
Prior AMG 706, oral inhibitors of AMG706, panitumumab, or another anti-EGFr monoclonal antibody (mAb) (e.g., cetuximab [Erbitux®] or EMD 72000)
Systemic chemotherapy within 28 days before study enrollment
Major surgery within 28 days or minor surgery within 7days of study enrollment
History of life threatening ventricular arrhythmia (eg, sustained ventricular tachycardia)
Female and male subjects of childbearing potential not using adequate contraceptive precautions
Participation in therapeutic clinical trials within 30 days before study enrollment
Not recovered from all previous therapies
Clinically significant open would, ulcer or fracture
Any co-morbid medical condition that would increase the risk of toxicity