drugset / Trial / NCT00101894

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

NCT00101894

Phase 1 Completed 119 enrolled Amgen
Non-randomizedParallel-groupOpen-labelTreatment

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.

Timeline

Start
2004-12
Primary completion
2010-04
Completion
2011-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Panitumumab Monoclonal antibody 6 mg/kg Intravenous
Subject motesanib Small molecule 50 mg Oral
Subject motesanib Small molecule 75 mg Oral
Subject motesanib Small molecule 100 mg Oral
Subject motesanib Small molecule 125 mg Oral
Background Irinotecan Small molecule
Background Leucovorin Small molecule 100 mg/m2 Intravenous
Background Leucovorin Small molecule 200 mg/m2 Intravenous
Background Oxaliplatin Small molecule 85 mg/m2 Intravenous
Background fluorouracil Small molecule 400 mg/m2 Intravenous
Background fluorouracil Small molecule 600 mg/m2 Intravenous