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New FDA Approval for KEYTRUDA®

Merck is pleased to announce that KEYTRUDA has been approved by the FDA for the adjuvant treatment of patients with melanoma with involvement of lymph node(s) following complete resection.

KEYTRUDA is also indicated for the treatment of patients with unresectable or metastatic melanoma.

·    PD-L1 diagnostic testing is not required prior to initiating treatment with KEYTRUDA in these patients

FDA=Food and Drug Administration; PD-L1=programmed death ligand 1.

KEYTRUDA® (pembrolizumab) Prescribing Information

The Medication Guide also is available.