China NMPA Accepts Hansoh Dalmelitinib NDA for EGFR-Mutant NSCLC

Reuters02-27

China NMPA Accepts Hansoh Dalmelitinib NDA for EGFR-Mutant NSCLC

Hansoh Pharmaceutical Group Co. Ltd. said China’s National Medical Products Administration has accepted a new drug application for dalmelitinib mesylate tablets used in combination with aumolertinib mesylate tablets (Ameile) to treat patients with locally advanced or metastatic EGFR mutation-positive non-small cell lung cancer whose tumors have MET amplification after prior EGFR tyrosine kinase inhibitor therapy. The company said dalmelitinib (HS-10241) is an oral, highly selective c-MET tyrosine kinase inhibitor it developed.

Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Hansoh Pharmaceutical Group Co. Ltd. published the original content used to generate this news brief via IIS, the Issuer Information Service operated by the Hong Kong Stock Exchange (HKex) (Ref. ID: HKEX-EPS-20260227-12032672), on February 27, 2026, and is solely responsible for the information contained therein.

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