Drug intelligence / Profile preview

Glucagon + GSK1362885

Development stage
Unknown
Lead developer
GSK
Modality
Recombinant Proteins and Enzymes, Small Molecules
Administration
Intranasal, Intramuscular, Intravenous, Subcutaneous, Oral
01

Overview

Glucagon + GSK1362885 is a combination of two agents with opposing mechanisms relevant to glucose metabolism. Glucagon is a 29-amino acid polypeptide hormone used primarily as an emergency treatment for severe hypoglycemia and as a diagnostic aid in radiologic exams to inhibit gastrointestinal motility. It acts by binding to the hepatic glucagon receptor, stimulating glycogenolysis and gluconeogenesis, thereby increasing blood glucose levels[2][4][5]. GSK1362885 is an investigational small molecule developed by GSK that functions as a potent inhibitor of human glycogen phosphorylase, aiming to reduce hepatic glucose output for the treatment of type 2 diabetes mellitus[6][8]. The combination would theoretically pair the hyperglycemic effect of glucagon with the hepatic glucose output-lowering action of a glycogen phosphorylase inhibitor; however, there are no known approved or clinically developed fixed-dose combinations of these two agents.

Other names
glucagon
02

Targets

PYG (Glycogen phosphorylase)GCGR (Glucagon receptor)

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