RSS China Approves Merck's Keytruda To Treat Patients With Resectable Stage II, IIIA Or IIIB NSCLC

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 RSS China Approves Merck's Keytruda To Treat Patients With Resectable Stage II, IIIA Or IIIB NSCLC

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Merck & Co Inc. (MRK) announced on Monday that China's National Medical Products Administration (NMPA) has granted approval for the use of Keytruda in combination with chemotherapy as a neoadjuvant treatment, followed by its use as an adjuvant therapy post-surgery for patients diagnosed with non-small cell lung cancer (NSCLC).

This approval is underpinned by the findings from the KEYNOTE-671 study, in which Keytruda was assessed alongside chemotherapy as a pre-surgical treatment and as a standalone therapy post-surgery for patients with stage II, IIIA, or IIIB NSCLC. The study's data demonstrated a 28% reduction in the risk of death with this treatment protocol.

This marks the fourth approved indication for Keytruda in the treatment of NSCLC in China.

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