【翰宇药业：司美格鲁肽注射液减重适应症已完成三期临床全部受试者入组】翰宇药业在互动平台上表示，公司的司美格鲁肽注射液按照2.2类进行上市申报，其中减重适应症于今年1月已完成三期临床全部受试者入组，目前正处于随访进行阶段，且项目已进入剂量维持期。未来三期临床完成后，公司将依据相关法规要求，整理完善临床试验数据后提交上市申请。

金融界2025-06-12

翰宇药业在互动平台上表示，公司的司美格鲁肽注射液按照2.2类进行上市申报，其中减重适应症于今年1月已完成三期临床全部受试者入组，目前正处于随访进行阶段，且项目已进入剂量维持期。未来三期临床完成后，公司将依据相关法规要求，整理完善临床试验数据后提交上市申请。

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