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Great news! Fulaimei®, China's first long-acting hypoglycemic agent independently researched and developed by Hansoh Pharma, was approved for marketing

2019.05.07 Size

On May 5, 2019, Hansoh’s Fulaimei® (Polyethylene Glycol Loxenatide for Injection) (available in 0.5ml:0.1mg and 0.5ml:0.2mg) received NDA approval from National Medical Products Administration.


Polyethylene Glycol Loxenatide is a GLP-1 receptor agonist. It is a Category 1.1 innovative drug, independently developed by Hansoh based on long-acting drug proprietary technology, for the treatment of type 2 diabetes. As a result of its molecular structure, Polyethylene Glycol Loxenatide only needs one injection per week to achieve a long-term effect.


 

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