Efficacy and Safety of a Single-Pill Combination of Vildagliptin and Metformin in Japanese Patients with Type 2 Diabetes Mellitus: A Randomized, Double-Blind, Placebo-Controlled Trial

被引:7
|
作者
Odawara, Masato [1 ]
Yoshiki, Mika [2 ]
Sano, Misako [2 ]
Hamada, Izumi [2 ]
Lukashevich, Valentina [3 ]
Kothny, Wolfgang [4 ]
机构
[1] Tokyo Med Univ, Dept Diabet Endocrinol Metab & Rheumatol, Tokyo 1608402, Japan
[2] Novartis Pharma KK, Tokyo, Japan
[3] Nova Pharmaceut Corp, E Hanover, NJ USA
[4] Novartis Pharma AG, Basel, Switzerland
关键词
Dipeptidyl peptidase-4 inhibitor; Metformin; Single-pill combination; Type 2 diabetes mellitus; Vildagliptin;
D O I
10.1007/s13300-015-0099-x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: The use of dipeptidyl peptidase-4 inhibitors in combination with metformin is increasing in Japanese patients with type 2 diabetes mellitus (T2DM), but no single-pill combination (SPC) is currently available in Japan. The objective of this study was to assess the efficacy and safety of vildagliptin/metformin SPC in Japanese patients with T2DM inadequately controlled with vildagliptin monotherapy. Methods: This was a 14-week, randomized, double-blind, parallel-group, placebo-controlled trial. 171 patients with T2DM inadequately controlled [HbA1c (glycosylated hemoglobin) 7.0-10.0%] with vildagliptin 50 mg twice daily (bid) were randomized (2: 1) to receive either a vildagliptin/metformin SPC (n = 115) or matching vildagliptin/placebo SPC (n = 56). Results: Baseline demographics and background characteristics were generally comparable between the treatment groups. The change in HbA1c [mean +/- standard error (SE)] was -0.8 +/- 0.1% in the vildagliptin/metformin SPC (baseline HbA1c, 7.9 +/- 0.1%) group and 0.1 +/- 0.1% in the vildagliptin/placebo SPC (baseline HbA1c, 8.0 +/- 0.1%) group, with a between-treatment difference of -1.0 +/- 0.1% (P<0.001) in favor of the vildagliptin/metformin SPC group. The proportion of patients achieving target HbA1c <7.0% was significantly higher with vildagliptin/metformin SPC compared with vildagliptin/placebo SPC (45.8% vs. 13.5%, P<0.001). The overall incidences of adverse events (AEs) were 43.5% in the vildagliptin/metformin SPC and 67.9% in the vildagliptin/placebo SPC group. The incidences of serious AEs were low in both the treatment groups (0.9% vs. 3.6%, respectively). Body weight remained constant throughout the study in both the treatment groups. There were no deaths or hypoglycemic events during the study. Conclusions: Switching Japanese patients with T2DM requiring treatment intensification, from vildagliptin monotherapy to a vildagliptin/metformin SPC (50/250 or 50/500 mg) was efficacious and safe, eliciting significant reduction in HbA1c without increased risk of hypoglycemia and weight gain.
引用
收藏
页码:17 / 27
页数:11
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