Drug intelligence / Profile preview

henagliflozin + retagliptin

Development stage
Unknown
Lead developer
Hengrui Pharmaceutical
Modality
Small Molecules
Administration
Oral
01

Overview

**Henagliflozin + retagliptin** is an oral fixed-dose combination therapy for type 2 diabetes mellitus. Henagliflozin is a sodium-glucose cotransporter 2 (SGLT2) inhibitor that lowers blood glucose by reducing renal glucose reabsorption, promoting urinary glucose excretion. Retagliptin is a dipeptidyl peptidase-4 (DPP-4) inhibitor that enhances the incretin system by inhibiting DPP-4, thereby increasing endogenous levels of active glucagon-like peptide-1 (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP), which stimulate insulin secretion and inhibit glucagon secretion in a glucose-dependent manner. The combination has shown superior glycemic efficacy compared to either agent alone in patients inadequately controlled with metformin, with added benefits on body weight and systolic blood pressure. No severe hypoglycemia was noted in studies[1][5]. Both drugs are being developed by Jiangsu Hengrui Medicine.

Brand names
HR20031HR-20031HR 20031
Other names
retagliptin + henagliflozinretagliptin phosphate + henagliflozin proline
02

Targets

DPP-4 (Dipeptidyl Peptidase-IV)SGLT2 (Sodium-glucose cotransporter protein subunit 2)SLC5A1 (Sodium Glucose Cotransporter 1)

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