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Pfizer Inc. (PFE)’s XALKORI® Receives Conditional Marketing Authorization From the European Commission (EC) for the Treatment of Adults With Previously Treated ALK-Positive Advanced Non-Small Cell Lung Cancer in the EU



10/24/2012 9:13:19 AM

NEW YORK--(BUSINESS WIRE)--Pfizer Inc. announced today that the European Commission has given conditional marketing authorization for XALKORI® (crizotinib) in the European Union (EU) for the treatment of adults with previously treated anaplastic lymphoma kinase (ALK)-positive advanced non-small cell lung cancer (NSCLC).

Read at BioSpace.com


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