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Pfizer Inc. (PFE)’s Crizotinib Receives Positive Opinion for Conditional Marketing Authorization From the Committee for Medicinal Products for Human Use for the Treatment Of Adults With Previously Treated ALK-Positive Advanced Non-Small Cell Lung Cancer in the EU  
7/20/2012 10:10:25 AM

NEW YORK--(BUSINESS WIRE)--Pfizer announced today that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) has adopted a positive opinion recommending that crizotinib be granted conditional marketing authorization 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).
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