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Non DPP-4 Inhibitor
A non-DPP-4 inhibitor that works through an alternative mechanism to manage blood glucose levels in diabetes, distinct from dipeptidyl peptidase-4 inhibition.
A non-DPP-4 inhibitor that works through an alternative mechanism to manage blood glucose levels in diabetes, distinct from dipeptidyl peptidase-4 inhibition. Used for Type 2 diabetes mellitus.
At a glance
| Generic name | Non DPP-4 Inhibitor |
|---|---|
| Sponsor | Chung-Ang University |
| Modality | Small molecule |
| Therapeutic area | Diabetes |
| Phase | FDA-approved |
Mechanism of action
This drug operates outside the DPP-4 inhibitor class, meaning it does not inhibit the dipeptidyl peptidase-4 enzyme. Without additional specificity on the exact mechanism from Chung-Ang University's research, the precise target pathway remains unclear, but it is positioned as a marketed antidiabetic agent with a differentiated mechanism of action from DPP-4 inhibitors.
Approved indications
- Type 2 diabetes mellitus
Common side effects
Key clinical trials
- Early Add-On Combination of GLP-1 Receptor Agonist and SGLT2 Inhibitor in People With Cardiovascular-Kidney-Metabolic Stage 2-3
- Dose Optimization of Sitagliptin and Duloxetine in Diabetic Cirrhosis (PHASE4)
- Oral Anti Diabetic Agents in the Hospital (PHASE4)
- A Pragmatic Randomized Trial to Evaluate the Comparative Effectiveness Between Dapagliflozin and Standard of Care in Type 2 Diabetes Patients (PHASE4)
- LIGHT-MCI Trial: GLP-1 Agonist, SGLT2 Inhibitor, and DPP-4 Inhibitor for MCI Remission in Type 2 Diabetes (NA)
- DPP4 Inhibitor Intervention on Post-stroke Cognitive Impairment in Ischemic Stroke Patients With Type 2 Diabetes (PHASE3)
- Second-line Therapies for Patients With Type 2 Diabetes and Moderate Cardiovascular Disease Risk
- DOORS: A Research Study to Understand How Oral Semaglutide Works in People With Type 2 Diabetes Who Change From Dipeptidyl Peptidase-4 Inhibitor (DPP4i) Treatment to Oral Semaglutide in Italy
Primary sources
Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.
| Source | Used for |
|---|---|
| ClinicalTrials.gov | Trial enrolment, design, endpoints, results |