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Merck Announces Third-Quarter 2023 Financial Results

FDA Approves KEYTRUDA® (pembrolizumab) for Treatment of Patients With Resectable (T?4 cm or N+) NSCLC in Combination With Chemotherapy as Neoadjuvant Treatment, Then Continued as a Single Agent as Adjuvant Treatment After Surgery

FDA Approves KEYTRUDA® (pembrolizumab) for Treatment of Patients With Resectable (T?4 cm or N+) NSCLC in Combination With Chemotherapy as Neoadjuvant Treatment, Then Continued as a Single Agent as Adjuvant Treatment After Surgery
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