Emerging GLP-1 receptor agonists

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Standard

Emerging GLP-1 receptor agonists. / Lund, Asger; Knop, Filip K; Vilsbøll, Tina.

I: Expert Opinion on Emerging Drugs, Bind 16, Nr. 4, 2011, s. 607-18.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Lund, A, Knop, FK & Vilsbøll, T 2011, 'Emerging GLP-1 receptor agonists', Expert Opinion on Emerging Drugs, bind 16, nr. 4, s. 607-18. https://doi.org/10.1517/14728214.2011.616493

APA

Lund, A., Knop, F. K., & Vilsbøll, T. (2011). Emerging GLP-1 receptor agonists. Expert Opinion on Emerging Drugs, 16(4), 607-18. https://doi.org/10.1517/14728214.2011.616493

Vancouver

Lund A, Knop FK, Vilsbøll T. Emerging GLP-1 receptor agonists. Expert Opinion on Emerging Drugs. 2011;16(4):607-18. https://doi.org/10.1517/14728214.2011.616493

Author

Lund, Asger ; Knop, Filip K ; Vilsbøll, Tina. / Emerging GLP-1 receptor agonists. I: Expert Opinion on Emerging Drugs. 2011 ; Bind 16, Nr. 4. s. 607-18.

Bibtex

@article{79c6800252624073998a33e9bfe43e2f,
title = "Emerging GLP-1 receptor agonists",
abstract = "Introduction: Recently, glucagon-like peptide-1 receptor (GLP-1R) agonists have become available for the treatment of type 2 diabetes. These agents exploit the physiological effects of GLP-1, which is able to address several of the pathophysiological features of type 2 diabetes. GLP-1R agonists presently available are administered once or twice daily, but several once-weekly GLP-1R agonists are in late clinical development. Areas covered: The present review aims to give an overview of the clinical data on the currently available GLP-1R agonists used for treatment of type 2 diabetes, exenatide and liraglutide, as well as the emerging GLP-1R agonists including the long-acting compounds. Expert opinion: An emerging therapeutic trend toward initial or early combination therapy with metformin- and incretin-based therapy is anticipated for patients with type 2 diabetes. GLP-1-based therapy has so far proven safe and tolerable. The determination of which incretin-based therapy to choose necessitates comparisons between the various GLP-1R agonists. The available GLP-1R agonists cause sustained weight loss and clinical relevant improvement of glycemic control. The long-acting GLP-1R agonists in late development may improve the effects of GLP-1 even further with optimized pharmacokinetic profiles resulting in fewer side effects. Meta-analyses have shown promising effects on cardiovascular disease and data from ongoing multicenter trials with cardiovascular endpoints are expected in 2015.",
author = "Asger Lund and Knop, {Filip K} and Tina Vilsb{\o}ll",
year = "2011",
doi = "http://dx.doi.org/10.1517/14728214.2011.616493",
language = "English",
volume = "16",
pages = "607--18",
journal = "Expert Opinion on Emerging Drugs",
issn = "1472-8214",
publisher = "Taylor & Francis",
number = "4",

}

RIS

TY - JOUR

T1 - Emerging GLP-1 receptor agonists

AU - Lund, Asger

AU - Knop, Filip K

AU - Vilsbøll, Tina

PY - 2011

Y1 - 2011

N2 - Introduction: Recently, glucagon-like peptide-1 receptor (GLP-1R) agonists have become available for the treatment of type 2 diabetes. These agents exploit the physiological effects of GLP-1, which is able to address several of the pathophysiological features of type 2 diabetes. GLP-1R agonists presently available are administered once or twice daily, but several once-weekly GLP-1R agonists are in late clinical development. Areas covered: The present review aims to give an overview of the clinical data on the currently available GLP-1R agonists used for treatment of type 2 diabetes, exenatide and liraglutide, as well as the emerging GLP-1R agonists including the long-acting compounds. Expert opinion: An emerging therapeutic trend toward initial or early combination therapy with metformin- and incretin-based therapy is anticipated for patients with type 2 diabetes. GLP-1-based therapy has so far proven safe and tolerable. The determination of which incretin-based therapy to choose necessitates comparisons between the various GLP-1R agonists. The available GLP-1R agonists cause sustained weight loss and clinical relevant improvement of glycemic control. The long-acting GLP-1R agonists in late development may improve the effects of GLP-1 even further with optimized pharmacokinetic profiles resulting in fewer side effects. Meta-analyses have shown promising effects on cardiovascular disease and data from ongoing multicenter trials with cardiovascular endpoints are expected in 2015.

AB - Introduction: Recently, glucagon-like peptide-1 receptor (GLP-1R) agonists have become available for the treatment of type 2 diabetes. These agents exploit the physiological effects of GLP-1, which is able to address several of the pathophysiological features of type 2 diabetes. GLP-1R agonists presently available are administered once or twice daily, but several once-weekly GLP-1R agonists are in late clinical development. Areas covered: The present review aims to give an overview of the clinical data on the currently available GLP-1R agonists used for treatment of type 2 diabetes, exenatide and liraglutide, as well as the emerging GLP-1R agonists including the long-acting compounds. Expert opinion: An emerging therapeutic trend toward initial or early combination therapy with metformin- and incretin-based therapy is anticipated for patients with type 2 diabetes. GLP-1-based therapy has so far proven safe and tolerable. The determination of which incretin-based therapy to choose necessitates comparisons between the various GLP-1R agonists. The available GLP-1R agonists cause sustained weight loss and clinical relevant improvement of glycemic control. The long-acting GLP-1R agonists in late development may improve the effects of GLP-1 even further with optimized pharmacokinetic profiles resulting in fewer side effects. Meta-analyses have shown promising effects on cardiovascular disease and data from ongoing multicenter trials with cardiovascular endpoints are expected in 2015.

U2 - http://dx.doi.org/10.1517/14728214.2011.616493

DO - http://dx.doi.org/10.1517/14728214.2011.616493

M3 - Journal article

VL - 16

SP - 607

EP - 618

JO - Expert Opinion on Emerging Drugs

JF - Expert Opinion on Emerging Drugs

SN - 1472-8214

IS - 4

ER -

ID: 40219274