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Merck: EC approves KEYTRUDA as adjuvant treatment for NSCLC

Merck announced that the European Commission has approved KEYTRUDA, Merck’s anti-PD-1 therapy, as a monotherapy for the adjuvant treatment of adults with non-small cell lung cancer who are at high risk of recurrence following complete resection and platinum-based chemotherapy. The decision marks fifth approval for KEYTRUDA in lung cancer in the EU.

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