Linagliptin plus metformin: a pharmacokinetic and pharmacodynamic evaluation

被引:11
作者
Scheen, Andre J. [1 ]
机构
[1] CHU Sart Tilman B35, Dept Med, Liege, Belgium
关键词
dipeptidyl peptidase-4 inhibitor; fixed-dose combination; linagliptin; metformin; pharmacokinetics; type 2 diabetes mellitus; TYPE-2; DIABETES-MELLITUS; DIPEPTIDYL PEPTIDASE-4 INHIBITOR; GLUCAGON-LIKE PEPTIDE-1; SELECTIVE DPP-4 INHIBITOR; ORAL ANTIDIABETIC AGENTS; ADD-ON THERAPY; DOUBLE-BLIND; GLYCEMIC CONTROL; CLINICAL PHARMACOKINETICS; COMBINATION THERAPY;
D O I
10.1517/17425255.2013.767892
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Introduction: The first-choice drug therapy in the management of type 2 diabetes is metformin. However, most patients require a combined therapy to reach and/or maintain targets of glucose control. Dipeptidyl peptidase-4 (DPP-4) inhibitors, commonly referred to as gliptins, offer new options for combined therapy with metformin. Linagliptin is the most recently launched gliptin, with a unique pharmacokinetic (PK) profile characterized by negligible renal excretion and is now also available as a fixed-dose combination (FDC) with metformin. Areas covered: An extensive literature search was performed to analyze the potential PK and pharmacodynamic interactions between linagliptin and metformin. Linagliptin and metformin may be administered together, either separately or as FDC supported by bioequivalence studies. Linagliptin and metformin are not prone to PK drug-drug interactions. Their coadministration improves blood glucose control more potently than either compound separately, without hypoglycemia and without increasing metformin-related gastrointestinal side effects. Expert opinion: The combination linaglitpin plus metformin, if not contraindicated (renal failure), may be used as first-line or second-line therapy in the management of type 2 diabetes. That being said, the durability of the glucose-lowering effect of this combination needs to be further explored in long-term controlled trials.
引用
收藏
页码:363 / 377
页数:15
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