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To compare the efficacy and safety of basal insulin peglispro (BIL), which has a flat pharmacokinetic and pharmacodynamic profile and a long duration of action, with insulin glargine (GL) in patients with type 1 diabetes.In this phase III, 52-week, blinded study, we randomized 1114 adults with type 1 diabetes in a 3 : 2 distribution to receive either BIL (n = 664) or GL (n = 450) at bedtime, with preprandial insulin lispro, using intensive insulin management. The primary objective was to compare glycated haemoglobin (HbA1c) in the groups at 52 weeks, with a non-inferiority margin of 0.4

作者:R M, Bergenstal;H, Lunt;E, Franek;F, Travert;J, Mou;Y, Qu;C J, Antalis;M L, Hartman;M, Rosilio;S J, Jacober;E J, Bastyr

来源:Diabetes, obesity & metabolism 2016 年 18卷 11期

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作者:
R M, Bergenstal;H, Lunt;E, Franek;F, Travert;J, Mou;Y, Qu;C J, Antalis;M L, Hartman;M, Rosilio;S J, Jacober;E J, Bastyr
来源:
Diabetes, obesity & metabolism 2016 年 18卷 11期
标签:
basal insulin glycaemic control hypoglycaemia randomized trial type 1 diabetes
To compare the efficacy and safety of basal insulin peglispro (BIL), which has a flat pharmacokinetic and pharmacodynamic profile and a long duration of action, with insulin glargine (GL) in patients with type 1 diabetes.In this phase III, 52-week, blinded study, we randomized 1114 adults with type 1 diabetes in a 3 : 2 distribution to receive either BIL (n = 664) or GL (n = 450) at bedtime, with preprandial insulin lispro, using intensive insulin management. The primary objective was to compare glycated haemoglobin (HbA1c) in the groups at 52 weeks, with a non-inferiority margin of 0.4

相似文献