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European Commission Approves Merck s KEYTRUDA® (pembrolizumab) Plus Chemotherapy as Neoadjuvant Treatment, Then Continued as Monotherapy as Adjuvant Treatment, for Resectable Non-Small Cell Lung Cancer (NSCLC) at High Risk of Recurrence in Adults

European Commission Approves Merck s KEYTRUDA® (pembrolizumab) Plus Chemotherapy as Neoadjuvant Treatment, Then Continued as Monotherapy as Adjuvant Treatment, for Resectable Non-Small Cell Lung Cancer (NSCLC) at High Risk of Recurrence in Adults
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United statesSolange petersExchange commissionEuropean commissionEuropean commission approves merckProduct serviceMerck co incCommittee for medicinal products humanStatement of merck co incCentre hospitalier universitaire vaudoisMerck research laboratoriesNeoadjuvant treatmentThen continuedAdjuvant treatmentResectable non small cell lung cancerHigh risk

Peer-to-peer KEYLearning series – Part 3: identifying adverse events

This video series and advertorial are fully funded and developed by MSD. Click the following links for prescribing information for Keytruda®

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