Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
DW1026C2 is a fixed-dose combination (FDC) therapy containing 100 mg of sitagliptin and 25 mg of empagliflozin. Developed by Daewon Pharmaceutical, it is indicated for the treatment of type 2 diabetes mellitus (T2DM) in patients who are inadequately controlled on metformin. The combination utilizes two distinct mechanisms of action: sitagliptin is a dipeptidyl peptidase-4 (DPP-4) inhibitor that increases active incretin levels to stimulate insulin secretion and suppress glucagon, while empagliflozin is a sodium-glucose cotransporter 2 (SGLT2) inhibitor that reduces renal glucose reabsorption, leading to increased urinary glucose excretion. This dual approach provides complementary glycemic control for patients with T2DM.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on sitagliptin + empagliflozin.