【博瑞医药:BGM504注射液获Ⅲ期临床试验批件】金十数据12月4日讯,博瑞医药公告,公司全资子公司博瑞新创自主研发的BGM504注射液降糖适应症的Ⅲ期临床研究方案已通过北京大学人民医院伦理审查委员会审批,获得伦理审查批件。BGM504注射液是GLP-1和GIP受体双重激动剂,属于境内外均未上市的化学药品1类创新药,展现多种代谢疾病治疗潜力。此前Ⅱ期临床试验结果显示,BGM504注射液在各剂量组的耐受性和安全性良好,降糖指标显著改善。公司将与北京大学人民医院等机构合作开展Ⅲ期临床研究。
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