Advancing Therapy in Suboptimally Controlled Basal Insulin-Treated Type 2 Diabetes: Clinical Outcomes With iGlarLixi Versus Premix BIAsp 30 in the SoliMix Randomized Controlled Trial

被引:36
|
作者
Rosenstock, Julio [1 ]
Emral, Rifat [2 ]
Sauque-Reyna, Leobardo [3 ]
Mohan, Viswanathan [4 ]
Trescoli, Carlos [5 ]
Al Sifri, Saud [6 ]
Lalic, Nebojsa [7 ]
Alvarez, Agustina [8 ]
Picard, Pascaline [9 ]
Bonnemaire, Mireille [10 ]
Demil, Nacima [11 ]
McCrimmon, Rory J. [12 ]
机构
[1] Dallas Diabet Res Ctr Med City, Dallas, TX 75230 USA
[2] Ankara Univ, Fac Med, Dept Endocrinol & Metab Dis, Ankara, Turkey
[3] Inst Diabet Obesidad & Nutr SC, Cuernavaca, Morelos, Mexico
[4] Dr Mohans Diabet Special Ctr & Madras Diabet Res, Ctr Adv Res Diabet, IDF Ctr Excellence Diabet Care & ICMR, Chennai, Tamil Nadu, India
[5] Hosp Univ La Ribera, Alzira, Spain
[6] Al Hada Mil Hosp, At Taif, Saudi Arabia
[7] Univ Belgrade, Clin Endocrinol, Clin Ctr Serbia, Fac Med, Belgrade, Serbia
[8] Sanofi, Buenos Aires, DF, Argentina
[9] IviData LIFE Sci, Levallois Perret, France
[10] Sanofi, Paris, France
[11] Sanofi, Diabet Med Operat Dept, Chilly Mazarin, France
[12] Univ Dundee, Sch Med, Div Syst Med, Dundee, Scotland
关键词
FIXED-RATIO COMBINATION; GLARGINE PLUS LIXISENATIDE; MELLITUS; EFFICACY; DEGLUDEC/LIRAGLUTIDE; LIRAGLUTIDE; PHYSICIANS; DEGLUDEC; LIXILAN; SAFETY;
D O I
10.2337/dc21-0393
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE To directly compare the efficacy and safety of a fixed-ratio combination, of insulin glargine 100 units/mL and the glucagon-like peptide 1 receptor agonist lixisenatide (iGlarLixi), with those of a premix insulin analog, biphasic aspart insulin 30 (30% insulin aspart and 70% insulin aspart protamine) (BIAsp 30) as treatment advancement in type 2 diabetes suboptimally controlled on basal insulin plus oral antihyperglycemic drugs (OADs). RESEARCH DESIGN AND METHODS In SoliMix, a 26-week, open-label, multicenter study, adults with suboptimally controlled basal insulin-treated type 2 diabetes (HbA(1c) >= 7.5% and <= 10%) were randomized to once-daily iGlarLixi or twice-daily BIAsp 30. Primary efficacy end points were noninferiority in HbA(1c) reduction (margin 0.3%) or superiority in body weight change for iGlarLixi versus BIAsp 30. RESULTS Both primary efficacy end points were met: after 26 weeks, baseline HbA(1c) (8.6%) was reduced by 1.3% with iGlarLixi and 1.1% with BIAsp 30, meeting noninferiority (least squares [LS] mean difference -0.2% [97.5% CI -0.4, -0.1]; P < 0.001). iGlarLixi was also superior to BIAsp 30 for body weight change (LS mean difference -1.9 kg [95% CI -2.3, -1.4]) and percentage of participants achieving HbA(1c) <7% without weight gain and HbA(1c) <7% without weight gain and without hypoglycemia (all P < 0.001). iGlarLixi was also superior versus BIAsp 30 for HbA(1c) reduction (P < 0.001). Incidence and rates of American Diabetes Association level 1 and 2 hypoglycemia were lower with iGlarLixi versus BIAsp 30. CONCLUSIONS Once-daily iGlarLixi provided better glycemic control with weight benefit and less hypoglycemia than twice-daily premix BIAsp 30. iGlarLixi is a more efficacious, simpler, and well-tolerated alternative to premix BIAsp 30 in suboptimally controlled type 2 diabetes requiring treatment beyond basal insulin plus OAD therapy.
引用
收藏
页码:2361 / 2370
页数:10
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