Liraglutide - overview of the preclinical and clinical data and its role in the treatment of type 2 diabetes

被引:58
作者
Davies, M. J. [1 ]
Kela, R. [2 ]
Khunti, K. [3 ]
机构
[1] Univ Leicester, Dept Cardiovasc Sci, Leicester LE1 5WW, Leics, England
[2] Univ Hosp Leicester NHS Trust, Leicester, Leics, England
[3] Univ Leicester, Dept Hlth Sci, Leicester LE1 5WW, Leics, England
关键词
beta cell; diabetes mellitus; GLP-1; analogue; glycaemic control; incretin-based therapy; incretin therapy; type; 2; diabetes; GLUCAGON-LIKE PEPTIDE-1; HUMAN GLP-1 ANALOG; IMPROVES GLYCEMIC CONTROL; BETA-CELL FUNCTION; PHARMACOKINETIC PROPERTIES; DERIVATIVE LIRAGLUTIDE; EXENATIDE EXENDIN-4; RECEPTOR AGONISTS; RENAL IMPAIRMENT; TREATED PATIENTS;
D O I
10.1111/j.1463-1326.2010.01330.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Type 2 diabetes is characterized by a progressive decline in glycaemic control. Many standard diabetes treatments, however, fail to achieve or maintain glycaemic control, and are often associated with an increased risk of hypoglycaemia and weight gain. Recently developed incretin-based therapies are a promising addition to the current armamentarium of diabetes treatments. Two types of incretin-based therapies are currently available: glucagon-like peptide (GLP)-1 receptor agonists (liraglutide and exenatide) and dipeptidyl peptidase-4 inhibitors (sitaglipin, vildagliptin and saxagliptin). This review aims to summarize the key efficacy and safety data of liraglutide, a once-daily human GLP-1 analogue. Extensive phase III clinical trials have shown liraglutide to improve glycaemic control with additional benefits on body weight, blood pressure and beta-cell function. Liraglutide is also generally well tolerated with a low risk of hypoglycaemia. Liraglutide has recently been approved for marketing in Europe, Japan and the USA.
引用
收藏
页码:207 / 220
页数:14
相关论文
共 50 条
[41]   Free fatty acid receptor agonists for the treatment of type 2 diabetes: drugs in preclinical to phase II clinical development [J].
Li, Zheng ;
Qiu, Qianqian ;
Geng, Xinqian ;
Yang, Jianyong ;
Huang, Wenlong ;
Qian, Hai .
EXPERT OPINION ON INVESTIGATIONAL DRUGS, 2016, 25 (08) :871-890
[42]   Is liraglutide or exenatide better in type 2 diabetes? [J].
Doggrell, Sheila A. .
EXPERT OPINION ON PHARMACOTHERAPY, 2009, 10 (16) :2769-2772
[43]   Preclinical discovery and development of colesevelam for the treatment of type 2 diabetes [J].
Nerild, Henriette Hoist ;
Christensen, Mikkel Bring ;
Knop, Filip Krag ;
Bronden, Andreas .
EXPERT OPINION ON DRUG DISCOVERY, 2018, 13 (12) :1161-1167
[44]   Early liraglutide treatment improves β-cell function in patients with type 2 diabetes: a retrospective cohort study [J].
Kondo, Yoshinobu ;
Satoh, Shinobu ;
Osada, Uru Nezu ;
Terauchi, Yasuo .
ENDOCRINE JOURNAL, 2015, 62 (11) :971-980
[45]   LIXISENATIDE FOR THE TREATMENT OF TYPE 2 DIABETES [J].
Petersen, A. B. ;
Knop, F. K. ;
Christensen, M. .
DRUGS OF TODAY, 2013, 49 (09) :537-553
[46]   Omarigliptin for the treatment of type 2 diabetes [J].
Tan, Xueying .
ENDOCRINE, 2016, 54 (01) :24-31
[47]   ALBIGLUTIDE FOR THE TREATMENT OF TYPE 2 DIABETES [J].
Muscogiuri, G. ;
Gastaldelli, A. .
DRUGS OF TODAY, 2014, 50 (10) :665-678
[48]   A Review of Efficacy and Safety Data Regarding the Use of Liraglutide, a Once-Daily Human Glucagon-Like Peptide 1 Analogue, in the Treatment of Type 2 Diabetes Mellitus [J].
Montanya, Eduard ;
Sesti, Giorgio .
CLINICAL THERAPEUTICS, 2009, 31 (11) :2472-2488
[49]   Type 2 diabetes: Where we are today: An overview of disease burden, current treatments, and treatment strategies [J].
Campbell, R. Keith .
JOURNAL OF THE AMERICAN PHARMACISTS ASSOCIATION, 2009, 49 :S3-S9
[50]   The incretin system and its role in type 2 diabetes mellitus [J].
Holst, Jens Juul ;
Vilsboll, Tina ;
Deacon, Carolyn F. .
MOLECULAR AND CELLULAR ENDOCRINOLOGY, 2009, 297 (1-2) :127-136