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SELINE: Second-Line Iressa Phase IV Study in NSCLC Patients — SELINE  

Non Small Cell Lung Carcinoma Clinical Trial

Official title:
A Phase IV, Multicenter, Non-randomized, Open-labeled Study to Evaluate the Efficacy of Gefitinib (IRESSA®) as a Second-line Therapy in NSCLC Patients

Clinical Trial Summary

The purpose of this study is to evaluate ORR (Objective Response Rate) of gefitinib as a second-line therapy for NSCLC patients based on RECIST (Response Evaluation Criteria in Solid Tumors Group) and check up ORR difference by EGFR mutation, gender, smoking history, and type of tumor.

Clinical Trial Description

n/a

Study Design

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00608868
Study type Interventional
Source AstraZeneca
Contact
Status Completed
Phase Phase 4
Start date January 2007
Completion date January 2009
View Details
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