Dual add-on therapy of gemigliptin and dapagliflozin in patients with type 2 diabetes inadequately controlled with metformin alone: The SOLUTION 2 study
- Authors
- Han, Kyung Ah; Hwang, You-Cheol; Moon, Shin Je; Cho, Ho Chan; Yoo, Hye Jin; Choi, Sung Hee; Chon, Suk; Kim, Kyoung-Ah; Kim, Tae Nyun; Kang, Jun Goo; Park, Cheol-Young; Won, Jong Chul; Cho, Eunjoo; Kim, Jeongyun; Park, Kyong Soo
- Issue Date
- Sep-2024
- Publisher
- John Wiley & Sons Ltd
- Keywords
- dapagliflozin; DPP-4 inhibitor; metformin; SGLT-2 inhibitor; type 2 diabetes
- Citation
- Diabetes, Obesity and Metabolism, v.26, no.9, pp 3743 - 3752
- Pages
- 10
- Indexed
- SCIE
SCOPUS
- Journal Title
- Diabetes, Obesity and Metabolism
- Volume
- 26
- Number
- 9
- Start Page
- 3743
- End Page
- 3752
- URI
- https://scholarworks.dongguk.edu/handle/sw.dongguk/22431
- DOI
- 10.1111/dom.15717
- ISSN
- 1462-8902
1463-1326
- Abstract
- Aim: To evaluate the efficacy and safety of gemigliptin and dapagliflozin dual add-on therapy (GEMI + DAPA) to metformin in type 2 diabetes (T2D) patients who had inadequate glycaemic control on metformin alone, compared with a single add-on of either gemigliptin (GEMI) or dapagliflozin (DAPA) to metformin. Materials and Methods: In this randomized, double-blind, double-dummy, active-controlled, parallel-group, phase 3 study, 469 T2D patients treated with a stable dose of metformin for 8 weeks or longer were randomized to receive GEMI + DAPA (n = 157) and either GEMI (n = 156) or DAPA (n = 156). The primary endpoint was change in HbA1c levels from baseline at week 24. Results: Baseline characteristics including body mass index and T2D duration were similar among groups. At week 24, the least square mean changes in HbA1c from baseline were -1.34% with GEMI + DAPA, -0.90% with GEMI (difference between GEMI + DAPA vs. GEMI -0.44% [95% confidence interval {CI}: -0.58% to -0.31%], P < .01) and -0.78% with DAPA (difference between GEMI + DAPA vs. DAPA -0.56% [95% CI: -0.69% to -0.42%], P < .01). Both upper CIs were less than 0, demonstrating the superiority of GEMI + DAPA for lowering HbA1c. The rates of responders achieving HbA1c less than 7% and less than 6.5% were greater with GEMI + DAPA (84.9%, 56.6%) than with GEMI (55.3%, 32.2%) and DAPA (49.3%, 15.3%). The incidence rate of adverse events was similar across groups, with low incidence rates of hypoglycaemia, urinary tract infection and genital infection. Conclusions: These results suggest that the addition of GEMI + DAPA to metformin as triple combination therapy was effective, safe and well-tolerated, especially for T2D patients who experienced poor glycaemic control on metformin alone.
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