drugset / Trial / NCT00160030

Study Comparing Radiochemotherapy With Folfox 4 Regimen or 5FU-Cisplatin in Patients With Inoperable Esophageal Cancer

NCT00160030 ↗

Phase 2 Completed 97 enrolled Sanofi
RandomizedParallel-groupOpen-labelTreatment

Summary

The primary objectives of this study are to assess the feasibility (completion of full treatment) in both arms and to assess endoscopic complete response rate in both arms. The secondary objective of this study is to assess the toxicity profile of each arm using the National Cancer Institute-Common Toxicity Criteria (NCI-CTC) scale (V.3).

Timeline

Start
2004-09
Primary completion
2007-10
Completion
—

Drugs

EvaluationDrugModalityDoseRoute
Comparator Cisplatin Other / unclassified — —
Comparator fluorouracil Small molecule — —

Indications