drugset / Trial / NCT00637091

Efficacy Analysis of Cetuximab Plus Irinotecan in Patients With Wild-type KRAS Without Regard to Epidermal Growth Factor Receptor (EGFR) Expressions

NCT00637091 ↗

Phase 2 Completed 40 enrolled Asan Medical Center
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to investigate the response rate of cetuximab plus irinotecan every 2 weeks in patients harboring wild-type KRAS with and without detectable EGFR-expressing metastatic CRC after failure to irinotecan in an exploratory manner.

Timeline

Start
2008-03
Primary completion
2009-09
Completion
2011-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Cetuximab Monoclonal antibody 500 mg/m2 —
Subject Irinotecan Small molecule 150 mg/m2 —
Subject Irinotecan Small molecule 180 mg/m2 —

Indications