Efficacy and safety of triple therapy with dapagliflozin add-on to saxagliptin plus metformin over 52 weeks in patients with type 2 diabetes

被引:59
作者
Mathieu, C. [1 ]
Herrera Marmolejo, M. [2 ]
Gonzalez Gonzalez, J. G. [3 ]
Hansen, L. [4 ]
Chen, H. [5 ]
Johnsson, E. [6 ]
Garcia-Sanchez, R. [5 ]
Iqbal, N. [5 ]
机构
[1] Katholieke Univ Leuven, Clin & Expt Endocrinol, Leuven, Belgium
[2] Torre Med, Serv Endocrinol, Guadalajara, Jalisco, Mexico
[3] Univ Autonoma Nuevo Leon, Serv Endocrinol, Monterrey, Mexico
[4] Bristol Myers Squibb, Global Clin Res Metabol, Princeton, NJ USA
[5] AstraZeneca, Global Med Dev, Gaithersburg, MD USA
[6] AstraZenca, Global Med Dev, Gothenburg, Sweden
关键词
dapagliflozin; DPP-4; inhibitor; metformin; SGLT2; type; 2; diabetes; RANDOMIZED CLINICAL-TRIALS; DOUBLE-BLIND; SULFONYLUREA; CANAGLIFLOZIN; SITAGLIPTIN;
D O I
10.1111/dom.12737
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We previously reported that dapagliflozin versus placebo as add-on to saxagliptin plus metformin resulted in greater reductions in glycated haemoglobin (A1C), fasting plasma glucose (FPG) and body weight (BW) after 24 weeks of treatment in patients with type 2 diabetes (T2D). Here we report results after 52 weeks of treatment. Patients stabilized on open-label metformin and saxagliptin 5 mg/day for 8-16 weeks were randomized to placebo or dapagliflozin 10 mg/day plus open-label saxagliptin plus metformin for 52 weeks. Changes from baseline to week 52 were greater with dapagliflozin versus placebo in A1C (-0.74% vs. 0.07%), FPG (-27 vs. 10 mg/dL) and BW (-2.1 vs. -0.4 kg). More patients achieved A1C <7% with dapagliflozin (29.4%) versus placebo (12.6%). Adverse events were similar with dapagliflozin (66%) and placebo (71%), and hypoglycaemia was rare (<= 2%). Genital infections occurred more often with dapagliflozin (6%) than with placebo (1%); frequency of urinary tract infections was similar between the two groups (9% vs. 10%). Triple therapy with dapagliflozin add-on to saxagliptin plus metformin is a durable, effective and well-tolerated intervention for the treatment of T2D.
引用
收藏
页码:1134 / 1137
页数:4
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