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圖16華東醫藥減重領域構建全方位差異化GLP-1靶點產品管線-行業數據

圖16華東醫藥減重領域構建全方位差異化GLP-1靶點產品管線
圖16華東醫藥減重領域構建全方位差異化GLP-1靶點產品管線
單靶點方面，公司利拉魯肽減重適應癥已獲批上市，為國內首款，同時打造口服制劑產品 HDM1002 ，目前已獲得中國和美國的 IND 批準，已于 2024 年 10 月獲得體重管理適應癥中國 II 期臨床研究的頂線結果，計劃 2024 年 Q4 遞交 pre-III 期溝通申請，并預計在 2025年 Q1開展體重管理適應癥臨床 III期試驗。同時，該產品正在中國開展糖尿病適應癥 II 期臨床研究。司美格魯肽注射液體重管理適應癥的 IND申請已于 2024年 9月底獲批。
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圖16華東醫藥減重領域構建全方位差異化GLP-1靶點產品管線_第1頁
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圖16華東醫藥減重領域構建全方位差異化GLP-1靶點產品管線_第2頁
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圖16華東醫藥減重領域構建全方位差異化GLP-1靶點產品管線_第8頁
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圖16華東醫藥減重領域構建全方位差異化GLP-1靶點產品管線_第9頁
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圖16華東醫藥減重領域構建全方位差異化GLP-1靶點產品管線_第11頁
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圖16華東醫藥減重領域構建全方位差異化GLP-1靶點產品管線_第19頁
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圖16華東醫藥減重領域構建全方位差異化GLP-1靶點產品管線_第32頁
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所屬報告： 華東醫藥-公司研究報告-跨越轉型步入新成長-241227（28頁）.pdf
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