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Teneligliptin + Sulfonylurea

Tanabe Pharma Corporation · Phase 3 active Small molecule

Teneligliptin inhibits dipeptidyl peptidase-4 (DPP-4) to increase incretin levels and lower blood glucose, while the sulfonylurea component stimulates pancreatic beta cells to release insulin.

Teneligliptin inhibits dipeptidyl peptidase-4 (DPP-4) to increase incretin levels and lower blood glucose, while the sulfonylurea component stimulates pancreatic beta cells to release insulin. Used for Type 2 diabetes mellitus.

At a glance

Generic nameTeneligliptin + Sulfonylurea
SponsorTanabe Pharma Corporation
Drug classDPP-4 inhibitor + Sulfonylurea combination
TargetDPP-4 enzyme; ATP-sensitive potassium channels on pancreatic beta cells
ModalitySmall molecule
Therapeutic areaDiabetes
PhasePhase 3

Mechanism of action

This is a fixed-dose combination where teneligliptin, a DPP-4 inhibitor, prolongs the action of glucagon-like peptide-1 (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP) to enhance glucose-dependent insulin secretion. The sulfonylurea component provides additional insulin secretion through direct beta-cell stimulation via ATP-sensitive potassium channel closure, offering complementary mechanisms for glycemic control in type 2 diabetes.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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