FDA Approved KEYTRUDA 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
Portfolio Pulse from Charles Gross
The U.S. Food and Drug Administration (FDA) has approved Merck's (NYSE:MRK) anti-PD-1 therapy, KEYTRUDA, for the treatment of patients with resectable non-small cell lung cancer (NSCLC). The approval is based on data from the Phase 3 KEYNOTE-671 trial, which showed significant improvements in event-free survival (EFS) and overall survival (OS).
October 16, 2023 | 11:02 pm
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Merck's KEYTRUDA has received FDA approval for the treatment of resectable NSCLC, potentially increasing the company's market share in the oncology sector.
FDA approval of a new indication for KEYTRUDA expands Merck's potential customer base, which could lead to increased sales and positively impact the company's stock price in the short term.
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