Contribution of Liraglutide in the Fixed-Ratio Combination of Insulin Degludec and Liraglutide (IDegLira)

被引:236
作者
Buse, John B. [1 ]
Vilsboll, Tina [2 ]
Thurman, Jerry [3 ]
Blevins, Thomas C. [4 ]
Langbakke, Irene H. [5 ]
Bottcher, Susanne G. [5 ]
Rodbard, Helena W. [6 ]
机构
[1] Univ N Carolina, Sch Med, Chapel Hill, NC 27515 USA
[2] Univ Copenhagen, Ctr Diabet Res, Gentofte Hosp, Copenhagen, Denmark
[3] SSM Med Grp, St Louis, MO USA
[4] Texas Diabet & Endocrinol, Austin, TX USA
[5] Novo Nordisk AS, Soborg, Denmark
[6] Endocrine & Metab Consultants, Clin Res, Rockville, MD USA
关键词
TREATED PATIENTS; TYPE-2; METFORMIN; INTENSIFICATION; MANAGEMENT; EXENATIDE; EFFICACY; SAFETY; INITIATION; BARRIERS;
D O I
10.2337/dc14-0785
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE Insulin degludec/liraglutide (IDegLira) is a novel combination of insulin degludec (IDeg) and liraglutide. This trial investigated the contribution of the liraglutide component of IDegLira versus IDeg alone on efficacy and safety in patients with type 2 diabetes. RESEARCH DESIGN AND METHODS In a 26-week, double-blind trial, patients with type 2 diabetes (A1C 7.5-10.0%[ 5886 mmol/mol]) on basal insulin (20-40 units) and metformin with or without sulfonylurea/glinides were randomized (1: 1) to once-daily IDegLira + metformin or IDeg + metformin with titration aiming for fasting plasma glucose between 4 and 5 mmol/L. Maximum allowed doseswere 50 dose steps (equal to 50 units IDeg plus 1.8 mg liraglutide) and 50 units for IDeg. The primary end point was change in A1C from baseline. RESULTS A total of 413 patients were randomized (mean A1C 8.8% [73 mmol/mol]; BMI 33.7 kg/m(2)). IDeg dose, alone or as part of IDegLira, was equivalent (45 units). A1C decreased by 1.9% (21 mmol/mol) with IDegLira and by 0.9% (10 mmol/mol) with IDeg (estimated treatment difference -1.1% [95% CI -1.3, -0.8], -12 mmol/mol [95% CI -14, -9; P < 0.0001). Mean weight reduction with IDegLira was 2.7 kg vs. no weight change with IDeg, P < 0.0001. Hypoglycemia incidence was comparable (24% for IDegLira vs. 25% for IDeg). Overall adverse events were similar, and incidence of nausea was low in both groups (IDegLira 6.5% vs. IDeg 3.5%). CONCLUSIONS IDegLira achieved glycemic control superior to that of IDeg at equivalent insulin doses without higher risk of hypoglycemia and with the benefit of weight loss. These findings establish the efficacy and safety of IDegLira and the distinct contribution of the liraglutide component.
引用
收藏
页码:2926 / 2933
页数:8
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