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Efficacy and safety of gemigliptin, a dipeptidyl peptidase-4 inhibitor, in patients with type 2 diabetes mellitus inadequately controlled with combination treatment of metformin and sulphonylurea: a 24-week, multicentre, randomized, double-blind, placebo-controlled study (TROICA study)

Authors
Ahn, Chang HoHan, Kyung AhYu, Jae MyungNam, Joo YoungAhn, Kyu JeungOh, Tae KeunLee, Hyoung WooLee, Dae HoKim, JaetaekChung, Choon HeePark, Tae SunKim, Byung JoonPark, Seok WonPark, Hyeong KyuLee, Kwang JaeKim, Sang-WookPark, Jeong HyunKo, Kwan PyoKim, Chong HwaLee, HyunjinJang, Hak ChulPark, Kyong Soo
Issue Date
May-2017
Publisher
WILEY
Keywords
clinical trial; DPP-4 inhibitor; phase III study
Citation
DIABETES OBESITY & METABOLISM, v.19, no.5, pp.635 - 643
Journal Title
DIABETES OBESITY & METABOLISM
Volume
19
Number
5
Start Page
635
End Page
643
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/6162
DOI
10.1111/dom.12866
ISSN
1462-8902
Abstract
Aims: To assess the efficacy and safety of gemigliptin, a dipeptidyl peptidase-4 inhibitor, added to metformin and sulphonylurea in patients with type 2 diabetes (T2DM). Materials and methods: We conducted a randomized, double-blind, placebo-controlled trial in 219 Korean patients inadequately controlled with metformin and glimepiride. Participants were randomized to gemigliptin 50 mg once daily or placebo added to metformin and glimepiride. The primary endpoint was change in glycated haemoglobin (HbA1c) level from baseline to week 24. Results: The baseline HbA1c was 8.2% in both groups. The addition of gemigliptin to metformin and glimepiride significantly reduced HbA1c levels at week 24 compared with placebo (between-group difference in adjusted mean change -0.87%, 95% confidence interval [CI] -1.09% to -0.64%). Fasting plasma glucose level was also significantly reduced with gemigliptin (-0.93 mmol/L, 95% CI -1.50 to -0.35 mmol/L), and a higher proportion of participants achieved an HbA1c level of < 7% (39.3% vs 5.5%; P<. 001) in the gemigliptin group than in the placebo group. Total cholesterol and LDL cholesterol were modestly but significantly reduced in the gemigliptin group compared with the placebo group (-0.21 mmol/L, 95% CI -0.38 to -0.03 mmol/L for total cholesterol, -0.18 mmol/L, 95% CI -0.34 to -0.01 mmol/L for LDL cholesterol). The incidence of hypoglycaemia was 9.4% in the gemigliptin group and 2.7% in the placebo group. Conclusions: Gemigliptin significantly improved glycaemic control in patients with T2DM inadequately controlled with metformin and sulphonylurea. The incidence of hypoglycaemia was higher with gemigliptin than with placebo, which highlights the importance of optimal dose adjustment for sulphonylurea.
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