New-Generation Glucokinase Activators: Potential Game-Changers in Type 2 Diabetes Treatment

被引:12
|
作者
Haddad, Dania [1 ]
Dsouza, Vanessa Sybil [1 ]
Al-Mulla, Fahd [1 ]
Al Madhoun, Ashraf [1 ,2 ]
机构
[1] Dasman Diabet Inst, Genet & Bioinformat Dept, Dasman 15462, Kuwait
[2] Dasman Diabet Inst, Anim & Imaging Core Facil, Dasman 15462, Kuwait
关键词
dorzagliatin; TTP399; glucokinase activator; type; 2; diabetes; clinical trials; safety; efficacy; BETA-CELL GLUCOKINASE; REGULATORY PROTEIN; MUTATIONS; SAFETY; DORZAGLIATIN; INHIBITORS; SECRETION; EFFICACY; MELLITUS; THERAPY;
D O I
10.3390/ijms25010571
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Achieving glycemic control and sustaining functional pancreatic beta-cell activity remains an unmet medical need in the treatment of type 2 diabetes mellitus (T2DM). Glucokinase activators (GKAs) constitute a class of anti-diabetic drugs designed to regulate blood sugar levels and enhance beta-cell function in patients with diabetes. A significant progression in GKA development is underway to address the limitations of earlier generations. Dorzagliatin, a dual-acting GKA, targets both the liver and pancreas and has successfully completed two phase III trials, demonstrating favorable results in diabetes treatment. The hepato-selective GKA, TTP399, emerges as a strong contender, displaying clinically noteworthy outcomes with minimal adverse effects. This paper seeks to review the current literature, delve into the mechanisms of action of these new-generation GKAs, and assess their efficacy and safety in treating T2DM based on published preclinical studies and recent clinical trials.
引用
收藏
页数:16
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