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Pathomolecular Analysis of Rare EGFR Mutations in Advanced NSCLC
This study has been completed.
Study NCT01215474 Information provided by Provitro GmbH
First Received on October 5, 2010. Last Updated on June 15, 2011
History of Changes
Related Studies can be found by searching for the Conditions, Interventions, and Sponsors found in this study:
Conditions listed in this trial
Mutations in Exons 18 to 21
Sponsors listed in this trial
Provitro GmbH
AstraZeneca
Charite University, Berlin, Germany
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