Lixisenatide for type 2 diabetes mellitus

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Lixisenatide for type 2 diabetes mellitus. / Christensen, Mikkel; Knop, Filip K; Vilsbøll, Tina; Holst, Jens Juul.

In: Expert Opinion on Investigational Drugs, Vol. 20, No. 4, 2011, p. 549-57.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Christensen, M, Knop, FK, Vilsbøll, T & Holst, JJ 2011, 'Lixisenatide for type 2 diabetes mellitus', Expert Opinion on Investigational Drugs, vol. 20, no. 4, pp. 549-57. https://doi.org/10.1517/13543784.2011.562191

APA

Christensen, M., Knop, F. K., Vilsbøll, T., & Holst, J. J. (2011). Lixisenatide for type 2 diabetes mellitus. Expert Opinion on Investigational Drugs, 20(4), 549-57. https://doi.org/10.1517/13543784.2011.562191

Vancouver

Christensen M, Knop FK, Vilsbøll T, Holst JJ. Lixisenatide for type 2 diabetes mellitus. Expert Opinion on Investigational Drugs. 2011;20(4):549-57. https://doi.org/10.1517/13543784.2011.562191

Author

Christensen, Mikkel ; Knop, Filip K ; Vilsbøll, Tina ; Holst, Jens Juul. / Lixisenatide for type 2 diabetes mellitus. In: Expert Opinion on Investigational Drugs. 2011 ; Vol. 20, No. 4. pp. 549-57.

Bibtex

@article{201d3a40cd9849dfa88c58cca3ec90ce,
title = "Lixisenatide for type 2 diabetes mellitus",
abstract = "Introduction: Type 2 diabetes mellitus (T2DM) is an increasing health problem worldwide. Glucagon-like peptide-1 (GLP-1) receptor agonists are an expanding drug class that target several of the pathophysiological traits of T2DM. Lixisenatide is a GLP-1 receptor agonist in development for once-daily treatment of T2DM. Areas covered: Pharmacological, preclinical and clinical evidence demonstrating the applicability of lixisenatide for the treatment of T2DM are reviewed. Available data and pending clinical development are summarized, critically appraised and compared to competitor drugs. The most relevant papers and meeting abstracts published up to November 2010 are used as sources for this review. Expert opinion: Efficacy and safety in T2DM are demonstrated with lixisenatide in monotherapy and in combination with metformin. However, limited data with the intended once-daily 20 µg subcutaneous dosing necessitate further evaluation of lixisenatide as add-on to various antidiabetic treatments. It remains to be established whether the slightly differing chemical properties compared to other GLP-1 receptor agonists including a rather short duration of action will be a disadvantage or maybe even an advantage, for example, when combined with long-acting insulin. Read More: http://informahealthcare.com/doi/abs/10.1517/13543784.2011.562191",
keywords = "Animals, Clinical Trials as Topic, Diabetes Mellitus, Type 2, Drug Evaluation, Preclinical, Drug Therapy, Combination, Glucagon-Like Peptide 1, Humans, Hypoglycemic Agents, Metformin, Peptides",
author = "Mikkel Christensen and Knop, {Filip K} and Tina Vilsb{\o}ll and Holst, {Jens Juul}",
year = "2011",
doi = "10.1517/13543784.2011.562191",
language = "English",
volume = "20",
pages = "549--57",
journal = "Current Opinion in Investigational Drugs",
issn = "1354-3784",
publisher = "Taylor & Francis",
number = "4",

}

RIS

TY - JOUR

T1 - Lixisenatide for type 2 diabetes mellitus

AU - Christensen, Mikkel

AU - Knop, Filip K

AU - Vilsbøll, Tina

AU - Holst, Jens Juul

PY - 2011

Y1 - 2011

N2 - Introduction: Type 2 diabetes mellitus (T2DM) is an increasing health problem worldwide. Glucagon-like peptide-1 (GLP-1) receptor agonists are an expanding drug class that target several of the pathophysiological traits of T2DM. Lixisenatide is a GLP-1 receptor agonist in development for once-daily treatment of T2DM. Areas covered: Pharmacological, preclinical and clinical evidence demonstrating the applicability of lixisenatide for the treatment of T2DM are reviewed. Available data and pending clinical development are summarized, critically appraised and compared to competitor drugs. The most relevant papers and meeting abstracts published up to November 2010 are used as sources for this review. Expert opinion: Efficacy and safety in T2DM are demonstrated with lixisenatide in monotherapy and in combination with metformin. However, limited data with the intended once-daily 20 µg subcutaneous dosing necessitate further evaluation of lixisenatide as add-on to various antidiabetic treatments. It remains to be established whether the slightly differing chemical properties compared to other GLP-1 receptor agonists including a rather short duration of action will be a disadvantage or maybe even an advantage, for example, when combined with long-acting insulin. Read More: http://informahealthcare.com/doi/abs/10.1517/13543784.2011.562191

AB - Introduction: Type 2 diabetes mellitus (T2DM) is an increasing health problem worldwide. Glucagon-like peptide-1 (GLP-1) receptor agonists are an expanding drug class that target several of the pathophysiological traits of T2DM. Lixisenatide is a GLP-1 receptor agonist in development for once-daily treatment of T2DM. Areas covered: Pharmacological, preclinical and clinical evidence demonstrating the applicability of lixisenatide for the treatment of T2DM are reviewed. Available data and pending clinical development are summarized, critically appraised and compared to competitor drugs. The most relevant papers and meeting abstracts published up to November 2010 are used as sources for this review. Expert opinion: Efficacy and safety in T2DM are demonstrated with lixisenatide in monotherapy and in combination with metformin. However, limited data with the intended once-daily 20 µg subcutaneous dosing necessitate further evaluation of lixisenatide as add-on to various antidiabetic treatments. It remains to be established whether the slightly differing chemical properties compared to other GLP-1 receptor agonists including a rather short duration of action will be a disadvantage or maybe even an advantage, for example, when combined with long-acting insulin. Read More: http://informahealthcare.com/doi/abs/10.1517/13543784.2011.562191

KW - Animals

KW - Clinical Trials as Topic

KW - Diabetes Mellitus, Type 2

KW - Drug Evaluation, Preclinical

KW - Drug Therapy, Combination

KW - Glucagon-Like Peptide 1

KW - Humans

KW - Hypoglycemic Agents

KW - Metformin

KW - Peptides

U2 - 10.1517/13543784.2011.562191

DO - 10.1517/13543784.2011.562191

M3 - Journal article

C2 - 21391833

VL - 20

SP - 549

EP - 557

JO - Current Opinion in Investigational Drugs

JF - Current Opinion in Investigational Drugs

SN - 1354-3784

IS - 4

ER -

ID: 34145317