Drug intelligence / Profile preview

luseogliflozin

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

Overview

Luseogliflozin is an orally active, second-generation small molecule inhibitor of sodium-glucose co-transporter 2 (SGLT2), developed for the treatment of type 2 diabetes mellitus. By selectively inhibiting SGLT2 in the renal proximal tubules, it reduces glucose reabsorption and promotes urinary glucose excretion, thereby lowering plasma glucose levels. Clinical studies have shown that it improves glycemic control and also provides additional metabolic benefits such as reductions in body weight, blood pressure, serum triglycerides, uric acid, and liver enzymes. Luseogliflozin was first approved in Japan in 2014 and is marketed under the brand name Lusefi[1][2][3][4][5].

Brand names
Lusefi
Other names
luseogliflozin hydratelusefiluseogliflozinaluseogliflozineluseogliflozinum
02

Targets

SGLT2 (Sodium-glucose cotransporter protein subunit 2)

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