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Clinical Trial Summary

The purpose of this study was to determine if AUY922 had superior efficacy when compared to chemotherapy agents docetaxel or pemetrexed in patients whose tumor had EGFR mutations.

The primary purpose of this study was to compare the efficacy of AUY922, when administered i.v. on a once-weekly schedule at 70 mg/m2, versus docetaxel or pemetrexed in adult patients with advanced NSCLC, whose tumors harbored EGFR activating mutations, and had developed resistance to EGFR TKI.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01646125
Study type Interventional
Source Novartis
Contact
Status Terminated
Phase Phase 2
Start date November 23, 2012
Completion date November 4, 2015