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FDA Approves Merck’s KEYTRUDA® (pembrolizumab) Plus Chemotherapy, With or Without Bevacizumab, as Treatment for Patients With Persistent, Recurrent or Metastatic Cervical Cancer Whose Tumors Express PD-L1 (CPS ≥1)

FDA Approves Merck's KEYTRUDA® (pembrolizumab) Plus Chemotherapy, With or Without Bevacizumab, as Treatment for Patients With Persistent, Recurrent or Metastatic Cervical Cancer Whose Tumors Express PD-L1 (CPS ≥1)

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KENILWORTH, N.J.–(BUSINESS WIRE)—- $MRK #MRK–FDA Approves Merck’s KEYTRUDA Plus Chemotherapy as Treatment for Patients With Persistent, Recurrent or Metastatic Cervical Cancer

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