Sihuan Pharmaceutical Wins FDA Fast Track for NG-350A in Rectal Cancer

Reuters
10/28
Sihuan Pharmaceutical Wins FDA <a href="https://laohu8.com/S/FTRK">Fast Track</a> for NG-350A in Rectal Cancer

Sihuan Pharmaceutical Holdings Group Ltd. announced that NG-350A, a product developed by its non-wholly owned subsidiary Xuanzhu Biopharmaceutical Co., Ltd. and licensed from Akamis Bio Ltd., has been granted Fast Track designation by the U.S. Food and Drug Administration (FDA). The designation is for the treatment of mismatch repair-proficient (pMMR) locally advanced rectal cancer (LARC). Xuanzhu Biopharm holds exclusive rights to develop, produce, and commercialize NG-350A in Greater China.

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. Sihuan Pharmaceutical Holdings Group Ltd. published the original content used to generate this news brief on October 28, 2025, and is solely responsible for the information contained therein.

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