智通财经APP获悉，8月17日，药物临床试验登记与信息公示平台官网显示，礼来(LLY.US)登记了一项Brenipatide注射液在成人抑郁症参与者中的III期临床研究。Insight数据库显示，Brenipatide是全球首个启动抑郁症III期临床的GLP-1类产品。

截图来源：药物临床试验登记与信息公示平台官网

Brenipatide是一款在研GLP1R/GIPR双激动剂，也是继替尔泊肽后，礼来第二款GLP-1/GIP双靶点新药，全球最高进度在Ⅲ期，尚未获批上市。除了抑郁症，礼来还启动了2项Brenipatide针对酒精使用障碍的III期研究。除此之外，礼来还在拓展其他适应症，包括双相情感障碍、哮喘、尼古丁依赖、精神分裂、腹泻型肠易激综合征、便秘型肠易激综合征、慢性阻塞性肺疾病等等。

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