757-P: Efficacy and Safety of Supaglutide Monotherapy in Patients with Type 2 Diabetes

Author:

WANG QINGHUA1,ZHOU YUE1,WANG WEIMIN1,TONG GUOYU1,JIA WEINA1,LI LIANG1,CHENG ZHIFENG1,LU YIBING1,SHI BIMIN1,BIAN FANG1,WANG YIHUA1,SHI XIAOXIA1,LI QINGJU1,SU XIUHAI1,WANG KUN1,YUAN GUOYUE1,LI LIPING1,LING HONGWEI1,HU XIAOLIN1,WANG YANGANG1,ZHAO NAIQING1,YANG YEHONG1,MA JIANHUA1,LI YIMING1,ZHU DALONG1

Affiliation:

1. Nanjing, China, Haerbin, China, Suzhou, China, Nanyang, China, Henan, China, Cangzhou, China, Zhenjiang, China, Luoyang, China, Xuzhou, China, Jinan, China, Qingdao, China, Shanghai, China

Abstract

GLP-1 is an incretin hormone with broad pharmacological potential. GLP-1 receptor agonists (GLP-1RAs) are successfully in clinical use for T2D and obesity. Several GLP-1-based therapies are in clinical evaluation for treating metabolic diseases. Supaglutide (supa), a novel GLP-1RA, is in late-stage development for T2D. The efficacy and safety of supa is being investigated in 297 patients with newly diagnosed T2D inadequately controlled with diet and exercise in this randomized, double-blind, placebo-controlled phase 3 clinical trial (NCT04994288). Supa treatment resulted in a statistically and clinically significant reduction from baseline in HbA1c at Week 24 of -1.73% and -2.15% with 1 and 3 mg QW dosing, respectively (p<0.001). Body weight was decreased by 0.97% and 3.14% from baseline in the supa 1 and 3 mg groups, respectively, with a significant difference for supa 3 mg versus 1 mg group (p<0.001). Supa also significantly improved glucose excursion, and increased meal-stimulated insulin and C-peptide secretion as determined by MMTT, suggesting improved glucose tolerance and enhanced β-cell function. The most common TEAEs with supa were GI symptoms, such as nausea, vomiting, diarrhea and decreased appetite, mostly in mild or moderate severity. Our data showed that supa improved glycemic and metabolic control and was well tolerated in T2D, suggesting supa as a novel alternative therapy for T2D and metabolic disorders. Disclosure Q.Wang: None. F.Bian: None. Y.Wang: None. X.Shi: None. Q.Li: None. X.Su: None. K.Wang: None. G.Yuan: None. L.Li: None. H.Ling: None. X.Hu: None. Y.Zhou: None. Y.Wang: None. N.Zhao: None. Y.Yang: None. J.Ma: None. Y.Li: None. D.Zhu: None. W.Wang: None. G.Tong: None. W.Jia: None. L.Li: None. Z.Cheng: None. Y.Lu: None. B.Shi: None.

Publisher

American Diabetes Association

Subject

Endocrinology, Diabetes and Metabolism,Internal Medicine

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