China CDE Grants GenFleet’s GFH375 Breakthrough Therapy Designation for KRAS G12D NSCLC

Reuters03-02

China CDE Grants GenFleet’s GFH375 Breakthrough Therapy Designation for KRAS G12D NSCLC

GenFleet Therapeutics (Shanghai) Inc. said the Center for Drug Evaluation of China’s National Medical Products Administration granted Breakthrough Therapy Designation to its oral KRAS G12D inhibitor GFH375 for treating KRAS G12D-mutant non-small cell lung cancer patients who have received at least one prior systemic therapy. The company said the designation was supported by Phase I/II data from the GFH375X1101 study.

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. Genfleet Therapeutics (Shanghai) Inc. 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-20260302-12033164), on March 02, 2026, and is solely responsible for the information contained therein.

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