Efsubaglutide alfa added to metformin improves glycaemia with β-cell functional responses in type 2 diabetes: a randomised, double-blind, placebo-controlled, two-stage adaptive phase 2b/3 trial (SUPER 2)

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Authors: Weiping Jia, Fei Gao, Jingyi Lu, Zhifeng Cheng, Xiaolin Dong, Xiaoxia Shi, Xiuhai Su, Liping Li, Wei Zhang, Yihua Wang, Jianhua Ma, Shu Li
+24 more Haifang Wang, Lin Cheng, Li Mao, Chengyan Jiang, Qingju Li, X.C. Li, Xin Zheng, Ming Liu, Jiao Sun, Hui Peng, Pan Huanfeng, Hongwei Ling, Chengxia Jiang, Junhua Song, Xi Zhang, Lili Zhang, Yang Liu, Tianshu Zeng, Yongcai Zhao, Yulong Xu, Yiming Li, Yuqian Bao, Jin Zhou, Qinghua Wang
Cited by: 1
References: 36

Abstract

Efsubaglutide alfa, a long-acting humanised GLP-1 receptor agonist, was evaluated as add-on therapy to metformin in adults with type 2 diabetes. In an operationally seamless adaptive phase 2b/3, randomised, double-blind, placebo-controlled trial, phase 2b randomised participants 1:1:1 to Efsubaglutide 1 mg, 3 mg, or placebo for 12 weeks; based on phase 2b efficacy and safety, an independent committee selected 3 mg as the recommended phase 3 dose. Phase 3 randomised new participants 1:1 to Efsubaglutide 3 mg or placebo for 24-week double-blind treatment, followed by a 28-week open-label extension. At week 12 in phase 2b, HbA1c decreased by 1.10% with 1 mg and 1.43% with 3 mg (both p < 0.0001). At week 24 in phase 3, HbA1c decreased by 1.80% with Efsubaglutide 3 mg versus 0.74% with placebo (estimated treatment difference, −1.06%; p < 0.001). Adverse events were predominantly mild to moderate gastrointestinal events. Trial registration: ClinicalTrials.gov NCT04998032. A randomised trial in metformin-treated type 2 diabetes found once-weekly efsubaglutide improved HbA1c and fasting glucose, reduced weight, and enhanced meal-stimulated insulin secretion with mainly mild GI side effects.

Fields of Study & Subjects

Diabetes Treatment and Management Metabolism Diabetes and Cancer Natural Antidiabetic Agents Studies

Publication details

Journal / source
Nature Communications
Publisher
Springer Science and Business Media LLC
Volume
17
Issue
1
Publication date
8 May 2026
Language
EN