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EU Approval Sought for Frontline Lazertinib Plus Amivantamab in EGFR+ NSCLC

A marketing authorization application seeking the approval of the combination of lazertinib and amivantamab in the first-line treatment of adult patients with advanced non­–small cell lung cancer harboring EGFR mutations has been submitted to the European Medicines Agency. ....

Catherine Taylor , European Medicines Agency , Janssen Pharmaceutical Companies Of Johnson , European Mediciens Agency , European Medicines , Therapy Area Strategy , Janssen Pharmaceutical Companies , European Medicines Agency , Lazertinib And Amivantamab , Phase 3 Mariposa Study ,