Keytruda® (pembrolizumab) – Expanded indication
April 11, 2019 - The FDA approved Merck’s Keytruda (pembrolizumab), as a single agent, for the first-line treatment of patients with stage III non-small cell lung cancer (NSCLC), who are not candidates for surgical resection or definitive chemoradiation, or metastatic NSCLC, and whose tumors express PD-L1 (Tumor Proportion Score [TPS] ≥ 1%) as determined by an FDA-approved test, with no EGFR or ALK genomic tumor aberrations.
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