Graefe-Mody E U, Padula S, Ring A, Withopf B, Dugi K A
Drug Metabolism and Pharmacokinetics, Boehringer Ingelheim Pharma GmbH & Co. KG, Birkendorfer Strasse 65, D-88397 Biberach/Riss, Germany.
Curr Med Res Opin. 2009 Aug;25(8):1963-72. doi: 10.1185/03007990903094361.
Linagliptin (BI 1356) is a novel, orally available inhibitor of dipeptidyl peptidase-4 (DPP-4). Linagliptin improves glycaemic control in type 2 diabetic patients by increasing the half-life of the incretin hormone glucagon-like peptide-1 (GLP-1). Linagliptin is expected to be used as monotherapy or in combination with other antihyperglycaemic agents. This study was conducted to investigate potential pharmacokinetic or pharmacodynamic interactions between linagliptin and metformin.
This randomised, monocentric, open-label, two-way crossover design study was conducted in 16 healthy male subjects. Linagliptin (10 mg/day) and metformin (850 mg three times daily) were each administered alone and concomitantly. The steady-state pharmacokinetics of linagliptin and metformin and the inhibition of DPP-4 activity were determined at the end of each dosing period.
Co-administration of linagliptin had no apparent effect on metformin exposure (metformin AUC(tau,ss); geometric mean ratio [GMR] co-administration:individual administration was 1.01; 90% confidence interval [CI] was 0.89-1.14). Effects on maximum concentration (C(max,ss)) were small (GMR: 0.89; 90% CI: 0.78-1.00). Co-administration of metformin did not significantly affect C(max,ss) of linagliptin (GMR: 1.03; 90% CI: 0.86-1.24), but increased AUC(tau)(,ss) by 20% (GMR: 1.20; 90% CI: 1.07-1.34). Metformin alone had no effect on DPP-4 activity, and the inhibition of DPP-4 caused by linagliptin was not affected by concomitant administration of metformin. Tolerability was good whether linagliptin and metformin were administered alone or concomitantly. No serious adverse events occurred and the frequency of adverse events was low; 7 events in 6 subjects. The most frequent events were related to the gastrointestinal tract, as expected with metformin. Importantly, no subjects experienced signs or symptoms relating to episodes of hypoglycaemia.
In this small, multiple dose study carried out in healthy subjects, co-administration of linagliptin with metformin did not have a clinically relevant effect on the pharmacokinetics or pharmacodynamics of either agent. This study suggests linagliptin and metformin can safely be administered concomitantly in type 2 diabetes patients without dose adjustment; larger, longer-term clinical trials in diabetic patients are underway.
利格列汀(BI 1356)是一种新型的口服二肽基肽酶-4(DPP-4)抑制剂。利格列汀通过延长肠促胰岛素激素胰高血糖素样肽-1(GLP-1)的半衰期来改善2型糖尿病患者的血糖控制。利格列汀有望用作单一疗法或与其他降糖药物联合使用。本研究旨在调查利格列汀与二甲双胍之间潜在的药代动力学或药效学相互作用。
本随机、单中心、开放标签、双向交叉设计研究在16名健康男性受试者中进行。利格列汀(10毫克/天)和二甲双胍(850毫克,每日三次)分别单独给药和联合给药。在每个给药期结束时测定利格列汀和二甲双胍的稳态药代动力学以及DPP-4活性的抑制情况。
联合使用利格列汀对二甲双胍的暴露量无明显影响(二甲双胍AUC(tau,ss);联合给药:单独给药的几何平均比值[GMR]为1.01;90%置信区间[CI]为0.89-1.14)。对最大浓度(C(max,ss))的影响较小(GMR:0.89;90% CI:0.78-1.00)。联合使用二甲双胍对利格列汀的C(max,ss)无显著影响(GMR:1.03;90% CI:0.86-1.24),但使AUC(tau)(,ss)增加了20%(GMR:1.20;90% CI:1.07-1.34)。单独使用二甲双胍对DPP-4活性无影响,利格列汀引起的DPP-4抑制不受二甲双胍联合给药的影响。无论利格列汀和二甲双胍单独给药还是联合给药,耐受性均良好。未发生严重不良事件,不良事件发生率较低;6名受试者出现7次事件。最常见的事件与胃肠道有关,这与二甲双胍的预期情况一致。重要的是,没有受试者出现与低血糖发作相关的体征或症状。
在这项针对健康受试者进行的小样本、多剂量研究中,利格列汀与二甲双胍联合使用对任何一种药物的药代动力学或药效学均无临床相关影响。本研究表明,利格列汀和二甲双胍可在2型糖尿病患者中安全联合给药,无需调整剂量;针对糖尿病患者的更大规模、更长期的临床试验正在进行中。