drugset / Trial / NCT00671437

Determine Tumor Response Using Fluorodeoxyglucose (FDG)- Positron Emission Tomography (PET)/Computed Tomography (CT) Before and After Cetuximab in Patients With Head and Neck Cancer

NCT00671437 ↗

Phase 2 Completed 42 enrolled Washington University School of Medicine
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to collect data and evaluate how the tumor is broken down in response to standard of care cetuximab treatment by evaluating the FDG-PET/CT scans, toxicity, see how well the FDG-PET/CT scans predict response to treatment and survival.

Timeline

Start
2008-06
Primary completion
2011-12
Completion
2015-08

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Cetuximab Monoclonal antibody 250 mg/m2 Intravenous