drugset / Trial / NCT00081315

Subcutaneous Amifostine (Ethyol®) in the Prevention of Radiochemotherapy-Induced Esophagitis and Pneumonitis in Patients With Unresectable Non-Small Cell Lung Cancer

NCT00081315

Phase 2 Completed 130 enrolled MedImmune LLC
RandomizedSingle-groupDouble-blindPrevention

Summary

The primary objective of this study is to assess the activity of subcutaneous (SC) amifostine on the incidence and severity of acute radiochemotherapy-induced esophagitis in patients with unresectable Stage IIIA or IIIB non-small cell lung cancer (NSCLC) receiving combined modality therapy.

Timeline

Start
2003-11
Primary completion
Completion
2006-08

Drugs

EvaluationDrugModalityDoseRoute
Subject amifostine Unknown Subcutaneous