HDM1005(poterepatide)注射液

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华东医药董秘陈波:完成体重管理适应症临床III期研究首例受试者入组
Quan Jing Wang· 2025-06-04 04:39
Group 1 - The 2025 Zhejiang Listed Companies Investor Online Reception Day and 2024 Annual Performance Briefing was held on May 13, 2025 [1] - East China Pharmaceutical's board secretary Chen Bo announced that the oral small molecule GLP-1 receptor agonist HDM1002 (conveglipron) completed the first subject enrollment for weight management indication in the Phase III clinical study in April 2025, with plans to complete all subject enrollments by the end of June 2025 [1] - The Phase II clinical study for diabetes indication is progressing smoothly, with topline results expected in Q3 2025 and entry into Phase III clinical research planned for the second half of 2025 [1] Group 2 - The GLP-1R/GIPR dual-target long-acting peptide agonist HDM1005 (poterepatide) is currently undergoing Phase II clinical trials for weight management indication, with all subjects enrolled by April 2025 and expected to enter Phase III clinical research in Q4 2025 [1] - The Phase II clinical trial for diabetes indication also completed the first subject enrollment in April 2025, and new indication IND applications for HDM1005 have been approved by NMPA for the treatment of obstructive sleep apnea (OSA) with obesity or overweight, and heart failure with preserved ejection fraction (HFpEF) with obesity or overweight [1] Group 3 - The FGF21R/GCGR/GLP-1R tri-target agonist DR10624 injection is currently conducting Phase II clinical research in China for the treatment of metabolic-associated fatty liver disease with high-risk liver fibrosis and metabolic-associated alcoholic fatty liver disease, with the first subject enrolled in April 2025 [2] - Another Phase II clinical study for DR10624 targeting severe hypertriglyceridemia in China has completed all patient enrollments, with topline results expected in Q3 2025 [2] - DR10624 has also received approval for clinical trial applications in China for type 2 diabetes and weight indications, and key research data for DR10624 in treating obesity with hypertriglyceridemia was presented at the EASL Congress 2025 in Amsterdam [2]
华东医药董秘陈波:GLP-1受体激动剂HDM1002完成体重管理适应症临床III期研究首例受试者入组
Quan Jing Wang· 2025-05-13 12:50
他指出,FGF21R/GCGR/GLP-1R三靶点激动剂DR10624注射液目前正在中国开展治疗合并肝纤维化高 风险的代谢相关脂肪性肝病以及代谢合并酒精相关脂肪变性肝病II期临床研究,并于2025年4月完成首 例受试者入组。与此同时,此前在中国已启动的另一项DR10624治疗重度高甘油三酯血症的II期临床研 究已完成全部患者入组,预计2025年第三季度获得揭盲后的顶线结果。DR10624用于2 型糖尿病和体重 适应症的中国临床试验申请也先后获批。此外,DR10624在新西兰治疗肥胖合并高甘油三脂血症的 Ib/IIa期临床研究结果在荷兰阿姆斯特丹举办的2025年欧洲肝病研究学会年会(EASL Congress 2025)上 首次发布,展示了DR10624在肥胖合并高甘油三酯血症受试者中取得的关键研究数据(详见公司于2025 年5月13日披露于巨潮资讯网的相关公告)。 2025年浙江辖区上市公司投资者网上集体接待日暨2024年度业绩说明会活动于5月13日在全景网举行。 陈波介绍,GLP-1R/GIPR双靶点长效多肽类激动剂HDM1005(poterepatide)注射液,正在开展体重管 理适应症II期临床试验,已 ...