诺和诺德口服GLP-1和胰淀素受体双重激动剂Amycretin片临床试验申请获中国国家药监局受理，开辟减重治疗新篇章，相关产业链受关注

金融界04-11

4月10日，中国国家药品监督管理局药品审评中心（CDE）在其官方网站上公示，丹麦医药巨头诺和诺德提交的1类新药Amycretin片临床试验申请已被正式受理。Amycretin是一种新型口服GLP-1受体和胰淀素受体长效共激动剂，被视为新一代的减重疗法。诺和诺德最近公开的一项小型1期临床研究表明，在接受12周该药物治疗后，患者的体重平均下降了13.1%，相较于安慰剂组的1.1%降幅显著。值得一提的是...

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