Efficacy and Safety of LixiLan, a Titratable Fixed-Ratio Combination of Insulin Glargine Plus Lixisenatide in Type 2 Diabetes Inadequately Controlled on Basal Insulin and Metformin: The LixiLan-L Randomized Trial

被引:223
作者
Aroda, Vanita R. [1 ]
Rosenstock, Julio [2 ]
Wysham, Carol [3 ]
Unger, Jeffrey [4 ]
Bellido, Diego [5 ]
Gonzalez-Galvez, Guillermo [6 ]
Takami, Akane [7 ]
Guo, Hailing [8 ]
Niemoeller, Elisabeth [9 ]
Souhami, Elisabeth [10 ]
Bergenstal, Richard M. [11 ]
机构
[1] Medstar Hlth Res Inst, Hyattsville, MD 20782 USA
[2] Dallas Diabet Res Ctr Med City, Dallas, TX USA
[3] Rockwood Clin, Spokane, WA USA
[4] Catalina Res Inst, Chino, CA USA
[5] Univ A Coruna, Complejo Hosp Univ Ferrol, La Coruna, Spain
[6] Univ Guadalajara, Inst Jalisciense Invest Diabet & Obesidad SC, Hosp Civil Guadalajara Dr Juan I Menchaca, Guadalajara, Jalisco, Mexico
[7] Sanofi, Tokyo, Japan
[8] BMD Consulting Inc, Biostat, Somerset, NJ USA
[9] Sanofi, Diabet Div, Frankfurt, Germany
[10] Sanofi, Diabet Div, Paris, France
[11] Pk Nicollet Hlth Serv, Int Diabet Ctr, Minneapolis, MN USA
关键词
ONCE-DAILY LIXISENATIDE; MELLITUS; THERAPY; 24-WEEK;
D O I
10.2337/dc16-1495
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE This study was conducted to demonstrate the efficacy and safety of LixiLan (iGlarLixi), a novel, titratable, fixed-ratio combination of insulin glargine (iGlar) (100 units) and lixisenatide, compared with iGlar in patients with type 2 diabetes inadequately controlled on basal insulin with or without up to two oral glucose lowering agents. RESEARCH DESIGN AND METHODS After a 6-week run-in when iGlar was introduced and/or further titrated, and oral antidiabetic drugs other than metformin were stopped, 736 basal insulin-treated patients (mean diabetes duration 12 years, BMI 31 kg/m(2)) were randomized 1:1 to open-label, once-daily iGlarLixi or iGlar, both titrated to fasting plasma glucose <100 mg/dL (<5.6 mmol/mol) up to a maximum dose of 60 units/day. The primary outcome was change in HbAi, levels at 30 weeks. RESULTS HbA(1c) decreased from 8.5% (69 mmol/mol) to 8.1% (65 mmol/mol) during the run-in period. After randomization, iGlarLixi showed greater reductions in HbAi, from baseline compared with iGlar (-1.1% vs. 0.6%, P < 0.0001), reaching a mean final HbAic of 6.9% (52 mmol/mol) compared with 7.5% (58 mmol/mol) for iGlar. HbA(1c) <7.0% (53 mmol/mol) was achieved in 55% of iGlarLixi patients compared with 30% on iGlar. Mean body weight decreased by 0.7 kg with iGlarLixi and increased by 0.7 kg with iGlar (1.4 kg difference, P < 0.0001). Documented symptomatic hypoglycemia (570 mg/dL) was comparable between groups. Mild gastrointestinal adverse effects were very low but more frequent with iGlarLixi. CONCLUSIONS Compared with iGlar, a substantially higher proportion of iGlarLixi-treated patients achieved glycemic targets with a beneficial effect on body weight, no additional risk of hypoglycemia, and low levels of gastrointestinal adverse effects in inadequately controlled, basal insulin-treated, long-standing type 2 diabetes.
引用
收藏
页码:1972 / 1980
页数:9
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