drugset / Trial / NCT00658658

Panitumumab in Children With Solid Tumors

NCT00658658

Phase 1 Completed 31 enrolled Amgen
NaSingle-groupOpen-labelTreatment

Summary

The primary objective of this study was to evaluate the safety and pharmacokinetics of up to 3 different dose schedules of panitumumab in pediatric patients with solid tumors.

Timeline

Start
2008-03
Primary completion
2015-03
Completion
2015-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Panitumumab Monoclonal antibody 2.5 mg/kg Intravenous
Subject Panitumumab Monoclonal antibody 6 mg/kg Intravenous
Subject Panitumumab Monoclonal antibody 9 mg/kg Intravenous

Indications