Efficacy Analysis of Cetuximab Plus Irinotecan in Patients With Wild-type KRAS Without Regard to Epidermal Growth Factor Receptor (EGFR) Expressions
- Sponsor
- Asan Medical Center
- Study ID
- NCT00637091
- Phase
- PHASE2
- Status
- Completed
Conditions
- Advanced Colorectal Cancer
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 75 Years
- Healthy Volunteers
- Not accepted
Interventions
- Cetuximab, irinotecan — DRUGcetuximab, irinotecan
Study Details
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.
Key Dates
- Start date
- Mar 31, 2008
- Status verified
- Jan 2021
- Primary completion
- Sep 30, 2009
- Completion
- Sep 30, 2011
Study Design
- Enrollment
- 40 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: EGFR expressionPatients' accrual will be adjusted by EGFR expression (positive vs. negative)
Primary Outcome Measure
Response rate [ Time Frame: 8 week ]
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