人福医药(600079.SH)公告称，公司全资子公司武汉人福创新药物研发中心有限公司近日在国家药品监督管理局药物临床试验登记与信息公示平台公示了II期临床试验登记信息，试验名称为“玉蚕颗粒治疗糖尿病肾脏疾病显性白蛋白尿的多中心、随机、双盲、安慰剂平行对照Ⅱ期临床试验”。试验目的是初步评价玉蚕颗粒治疗糖尿病肾脏疾病显性白蛋白尿的有效性与安全性并探索剂量，为III期临床研究提供依据。玉蚕颗粒由创新药研发中心和上海复活石医药科技有限公司联合开发及申报，于2024年11月获得国家药品监督管理局颁发的《药物临床试验批准通知书》。截至目前该项目累计研发投入约为人民币900万元。
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