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Sitagliptin/Empagliflozin FDC Improves Glycaemic Control with Good Safety: Study

Written By : Dr. Shravani Dali Published On 2026-04-03T09:30:34+05:30  |  Updated On 3 April 2026 10:50 AM IST
Sitagliptin/Empagliflozin FDC Improves Glycaemic Control with Good Safety: Study
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Researchers have found in a new study that fixed-dose combination of sitagliptin and empagliflozin significantly improved glycaemic control at 24 weeks, with sustained benefits up to 52 weeks. The therapy demonstrated a favorable safety profile, including a very low risk of hypoglycaemia.

Type 2 diabetes mellitus (T2DM) is a progressive, multi-organ disorder that often requires intensive combination therapy. This Phase III, randomised, double-blind, placebo-controlled study evaluated the efficacy and safety of two fixed-dose combinations (FDCs) of sitagliptin 100 mg with empagliflozin 10 mg (DW1026C1) or empagliflozin 25 mg (DW1026C2) as add-on therapy for patients with inadequately controlled T2DM.

Two hundred thirty adults with T2DM inadequately controlled by metformin (≥ 1000 mg/day) and sitagliptin (100 mg) were 1:1:1 randomised to receive DW1026C1 (E10 group, n = 77), DW1026C2 (E25 group, n = 76), or a placebo (n = 77). Treatment was administered for 24 weeks, followed by a 28-week extension period. The primary endpoint was the change in HbA1c from baseline to Week 24.

Baseline characteristics were similar among groups. At Week 24, both active treatments demonstrated statistically significant HbA1c reductions versus the placebo. The least square mean differences [95% CI] versus the placebo were −0.54% [−0.78, −0.29] for E10 group and −0.61% [−0.85, −0.36] for E25 group (both p < 0.0001). Fasting plasma glucose (FPG), insulin resistance, body weight, systolic blood pressure, albumin-creatinine ratio and high-density lipoprotein cholesterol also improved in the active groups. Reductions in HbA1c, FPG and insulin resistance were sustained in Week 52. Safety profiles were favourable with adverse events similar in frequency and no increased hypoglycaemia risk.

Sitagliptin/empagliflozin FDC doses achieved improvements in glycaemic control at 24 weeks, which was maintained through 52 weeks. These benefits were accompanied by a favourable safety profile, including a very low risk of hypoglycaemia.


Reference:

S.Lim, T. N.Kim, J. O.Mok, et al., “Efficacy and Safety of Fixed-Dose Combinations of Sitagliptin and Empagliflozin as Add-On to Metformin in Korean Patients With Type 2 Diabetes: A Randomised, Double-Blind, Multi-Centre, Placebo-Controlled, Phase III Trial,” Diabetes, Obesity and Metabolism (2026): 1–13, https://doi.org/10.1111/dom.70669.


Keywords:

Sitagliptin/Empagliflozin, FDC, Improves, Glycaemic Control, Good Safety, Study, S.Lim, T. N.Kim, J. O.Mok,Diabetes, Obesity and Metabolism




Sitagliptin/EmpagliflozinFDCImprovesGlycaemic ControlGood SafetyStudyDiabetesObesity and Metabolism
Source : Diabetes, Obesity and Metabolism
Dr. Shravani Dali
Dr. Shravani Dali

    Dr. Shravani Dali has completed her BDS from Pravara institute of medical sciences, loni. Following which she extensively worked in the healthcare sector for 2+ years. She has been actively involved in writing blogs in field of health and wellness. Currently she is pursuing her Masters of public health-health administration from Tata institute of social sciences. She can be contacted at editorial@medicaldialogues.in.

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