drugset / Trial / NCT00091806

Two Dose Schedules of Panitumumab in Subjects With Advanced Solid Tumors

NCT00091806

Phase 1 Completed 86 enrolled Amgen
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the safety and pharmacokinetics of two dose schedules of panitumumab in subjects with advanced solid tumors.

Timeline

Start
2004-08
Primary completion
2006-04
Completion
2006-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Panitumumab Monoclonal antibody 6 mg/kg Intravenous
Subject Panitumumab Monoclonal antibody 9 mg/kg Intravenous

Indications