Exenatide

被引:62
作者
Barnett, A.
机构
[1] Birmingham Heartlands Hosp, Undergrad Ctr, Birmingham B9 5SS, W Midlands, England
[2] Heart England NHS Fdn Trust, Birmingham, W Midlands, England
[3] Univ Birmingham, Birmingham B15 2TT, W Midlands, England
关键词
exenatide; exenatide LAR; glucagon-like peptide-1; incretin mimetic; Type; 2; diabetes;
D O I
10.1517/14656566.8.15.2593
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Exenaticle is the first in a new class of compounds, which possess similar activity to the naturally-occurring hormone glucagon-like pepticle-1 (GLP-1). It mirrors many of the effects of GLP-1, improving glycaemic control through a combination of mechanisms, which include glucose-dependent stimulation of insulin secretion, suppression of glucagon secretion, slowing of gastric emptying and reduced appetite. Phase III clinical trials showed exenaticle therapy for 30 weeks significantly reduced glycated haemoglobin, and fasting and postprandial plasma glucose compared with baseline when added to metformin and sulfonylureas or a combination of the two, with an average weight loss of similar to 2 kg. Exenaticle can also be used in combination with thiazoliclinediones and may be an alternative to insulin in patients requiring additional therapy. In patients with established Type 2 diabetes, control of both glycaemia and body weight are important to minimise the risk of future diabetes complications. Open-label extensions from these pivotal trials demonstrate that patients treated with exenaticle for ! 3 years sustained the reductions in glycaemic control achieved at 30 weeks and had a progressive reduction in body weight. Exenaticle is generally well tolerated; nausea is the most commonly reported side effect, but can be significantly reduced when a target dose of exenaticle is achieved in patients with gradual dose titration. Hypoglycaemia has been encountered in clinical trials of exenaticle, especially on initiation of therapy with sulfonylureas (not with metformin). Exenatide may enable patients with Type 2 diabetes to improve glycaemic control and reduce or eliminate the risk of hypoglycaemia and weight gain.
引用
收藏
页码:2593 / 2608
页数:16
相关论文
共 67 条
[1]   Gut peptides and type 2 diabetes mellitus treatment [J].
Bo Ahrén .
Current Diabetes Reports, 2003, 3 (5) :365-372
[2]   Effect of exenatide on β cell function after islet transplantation in type 1 diabetes [J].
Al Ghofaili, Khalid ;
Fung, Michelle ;
Ao, Ziliang ;
Meloche, Mark ;
Shapiro, R. Jean ;
Warnock, Garth L. ;
Elahi, Darlush ;
Meneilly, Graydon S. ;
Thompson, David M. .
TRANSPLANTATION, 2007, 83 (01) :24-28
[3]   A recombinant human glucagon-like peptide (GLP)-1-albumin protein (Albugon) mimics peptidergic activation of GLP-1 receptor-dependent pathways coupled with satiety, gastrointestinal motility, and glucose homeostasis [J].
Baggio, LL ;
Huang, QL ;
Brown, TJ ;
Drucker, DJ .
DIABETES, 2004, 53 (09) :2492-2500
[4]  
BHATIA R, 2006, PROGR ABSTR AM DIAB
[5]   Pharmacokinetics of an oral drug (acetaminophen) administered at various times in relation to subcutaneous injection of exenatide (exendin-4) in healthy subjects [J].
Blase, E ;
Taylor, K ;
Gao, HY ;
Wintle, M ;
Fineman, M .
JOURNAL OF CLINICAL PHARMACOLOGY, 2005, 45 (05) :570-577
[6]   Interim analysis of the effects of exenatide treatment on A1C, weight and cardiovascular risk factors over 82 weeks in 314 overweight patients with type 2 diabetes [J].
Blonde, L. ;
Klein, E. J. ;
Han, J. ;
Zhang, B. ;
Mac, S. M. ;
Poon, T. H. ;
Taylor, K. L. ;
Trautmann, M. E. ;
Kim, D. D. ;
Kendall, D. M. .
DIABETES OBESITY & METABOLISM, 2006, 8 (04) :436-447
[7]  
BUSE J, 2007, PROGR ABSTR 67 SCI S
[8]   Effects of exenatide (exendin-4) on glycemic control over 30 weeks in sulfonylurea-treated patients with type 2 diabetes [J].
Buse, JB ;
Henry, RR ;
Han, J ;
Kim, DD ;
Fineman, MS ;
Baron, AD .
DIABETES CARE, 2004, 27 (11) :2628-2635
[9]   Metabolic effects of two years of exenatide treatment on diabetes, obesity, and hepatic biomarkers in patients with type 2 diabetes: An interim analysis of data from the open-label, uncontrolled extension of three double-blind, placebo-controlled trials [J].
Buse, John B. ;
Klonoff, David C. ;
Nielsen, Loretta L. ;
Guan, Xuesong ;
Bowlus, Christopher L. ;
Holcombe, John H. ;
Maggs, David G. ;
Wintle, Matthew E. .
CLINICAL THERAPEUTICS, 2007, 29 (01) :139-153
[10]   A randomized, open-label, crossover study examining the effect of injection site on bioavallability of exenatide (synthetic exendin-4) [J].
Calara, F ;
Taylor, K ;
Han, J ;
Zabala, E ;
Carr, EM ;
Wintle, M ;
Fineman, M .
CLINICAL THERAPEUTICS, 2005, 27 (02) :210-215