Long-term safety and efficacy of linagliptin as monotherapy or in combination with other oral glucose-lowering agents in 2121 subjects with type 2 diabetes: up to 2 years exposure in 24-week phase III trials followed by a 78-week open-label extension

被引:32
作者
Gomis, R. [1 ]
Owens, D. R. [2 ]
Taskinen, M. -R. [3 ]
Del Prato, S. [4 ]
Patel, S. [5 ]
Pivovarova, A. [6 ]
Schlosser, A. [7 ]
Woerle, H. -J. [8 ]
机构
[1] Univ Barcelona, CIBERDEM, IDIBAPS, Endocrinol & Diabet Serv,Hosp Clin, Barcelona, Spain
[2] Cardiff Univ, Ctr Endocrinol & Diabet Sci, Cardiff, S Glam, Wales
[3] Univ Helsinki, Cent Hosp, Dept Med, Helsinki, Finland
[4] Univ Pisa, Dept Endocrinol & Metab, Pisa, Italy
[5] Boehringer Ingelheim GmbH & Co KG, Bracknell, Berks, England
[6] Boehringer Ingelheim GmbH & Co KG, Biberach, Germany
[7] Boehringer Ingelheim GmbH & Co KG, Alkmaar, Netherlands
[8] Boehringer Ingelheim KG, D-6507 Ingelheim, Germany
关键词
PEPTIDASE-4; INHIBITORS; ACUTE-PANCREATITIS; GLYCEMIC CONTROL; POOLED ANALYSIS; METFORMIN; THERAPY; SITAGLIPTIN; MELLITUS; ROSIGLITAZONE; SULFONYLUREA;
D O I
10.1111/j.1742-1241.2012.02975.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aim: The aim of this study was to evaluate the long-term safety, tolerability and efficacy of the dipeptidyl peptidase-4 inhibitor linagliptin given either alone or in combination with other oral glucose-lowering agents in persons with type 2 diabetes. Methods: A 78-week open-label extension study evaluated subjects who participated in one of four preceding 24-week, randomised, double-blind, placebo-controlled parent trials and who received linagliptin, linagliptin + metformin, linagliptin + metformin + a sulphonylurea or linagliptin + pioglitazone (all with linagliptin administered orally once daily). Individuals receiving one of these treatments during a previous trial continued the same treatment (n = 1532) for up to a total of 102 weeks, whereas those previously receiving placebo were switched to linagliptin (n = 589). All 2121 participants received at least one dose of the trial medication and were included in the primary safety analysis. Results: In subjects previously receiving active treatment, the glycosylated haemoglobin A1c reduction achieved during the 24-week parent trials was sustained through the 78-week extension period (change from baseline to week 102: -0.8%). Drug-related adverse events were experienced by 14.3% of participants. Hypoglycaemia occurred in 13.9% of participants and was similar between those previously receiving treatment (13.6%) and those switching from placebo to linagliptin (14.6%). Hypoglycaemia occurred most frequently with the use of metformin + a sulphonylurea background therapy (11%). Overall, no clinically relevant changes in body weight were observed. Conclusion: Long-term treatment with linagliptin was well tolerated with no change in the safety profile observed during the extension study. Sustained long-term glycaemic control was maintained for up to 102 weeks with either linagliptin monotherapy or linagliptin in combination with other oral glucose-lowering agents.
引用
收藏
页码:731 / 740
页数:10
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