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Clinical Trial Summary

1. Trial design: Prospective observational study 2. Target population: 200 NSCLC patients with histologically or cytologically confirmed stage IV or recurrent NSCLC who have progressive disease after 1st line chemotherapy who consent for study participation and meet the study selection criteria 3. Primary objective: To investigate C-met expression/amplification and EGFR gene mutations in NSCLC patients treated with Erlotinib - C-met expression by IHC C-met amplification by SISH EGFR mutation by real time PCR 4. We will also assess the correlation of EGFR mutations and c-MET with clinical outcome (Overall Response Rate, Progression Free survival ) 5. Duration of Trial Recruitment: 2 years


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01523340
Study type Observational
Source Chonnam National University Hospital
Contact
Status Completed
Phase
Start date September 2011
Completion date November 2017

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