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dapagliflozin + sitagliptin (AstraZeneca)

Development stage
Unknown
Lead developer
AstraZeneca
Modality
Small Molecules
Administration
Oral
01

Overview

This reference drug entity represents the co-administration of the sodium-glucose co-transporter 2 (SGLT2) inhibitor dapagliflozin and the dipeptidyl peptidase-4 (DPP-4) inhibitor sitagliptin. In the context of clinical development by Chong Kun Dang Pharmaceutical, this combination (referred to by the internal codes D759 and D308) serves as the reference comparator in Phase 1 pharmacokinetic and safety studies for the fixed-dose combination product CKD-389. Dapagliflozin reduces renal glucose reabsorption, leading to urinary glucose excretion, while sitagliptin increases the levels of active incretin hormones, enhancing insulin secretion and decreasing glucagon levels. Both components are established, orally administered treatments for type 2 diabetes mellitus, providing complementary glycemic control through renal and incretin-based pathways.

Brand names
FarxigaJanuviaForxiga
Other names
dapagliflozin and sitagliptin co-administration
02

Targets

SGLT2 (Sodium-glucose cotransporter protein subunit 2)

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