China NMPA Grants Priority Review to HUTCHMED's Savolitinib NDA for MET-Amplified Gastric Cancer

Reuters2025-12-30

China NMPA Grants Priority Review to HUTCHMED's Savolitinib NDA for MET-Amplified Gastric Cancer

HUTCHMED (China) Ltd. announced that its New Drug Application (NDA) for savolitinib, a selective MET inhibitor, has been accepted and granted priority review by the China National Medical Products Administration (NMPA) for the treatment of locally advanced or metastatic gastric cancer or gastroesophageal junction adenocarcinoma patients with MET amplification who have failed at least two prior systemic treatments. This regulatory review is supported by positive Phase II study data and follows the Breakthrough Therapy Designation granted to savolitinib in 2023. If approved, savolitinib could become the first selective MET inhibitor available in China for this patient population.

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. HUTCHMED (China) Ltd. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW9618143-en) on December 30, 2025, and is solely responsible for the information contained therein.

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