歌礼制药-B向美国FDA提交ASC30_39 FDC临床试验申请,该口服小分子固定剂量复方制剂有望成为治疗肥胖症的同类首创GLP-1R激动剂与选择性胰淀素受体激动剂组合

美股速递
Nov 11

歌礼制药-B已正式向美国食品药品监督管理局(FDA)递交ASC30_39 FDC的新药临床试验(IND)申请。该药物是一种口服小分子固定剂量复方制剂,将GLP-1R激动剂与选择性胰淀素受体激动剂合二为一,拟用于肥胖症治疗,并具备成为同类首创(first-in-class)疗法的潜力。

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