Clinical Considerations When Initiating and Titrating Insulin Degludec/Liraglutide (IDegLira) in People with Type 2 Diabetes

Publikation: Bidrag til tidsskriftReviewForskningfagfællebedømt

Standard

Clinical Considerations When Initiating and Titrating Insulin Degludec/Liraglutide (IDegLira) in People with Type 2 Diabetes. / Harris, Stewart; Abrahamson, Martin J.; Ceriello, Antonio; Charpentier, Guillaume; Evans, Marc; Lehmann, Roger; Liebl, Andreas; Linjawi, Sultan; Holt, Richard I.G.; Hosszúfalusi, Nóra; Rutten, Guy; Vilsbøll, Tina.

I: Drugs, Bind 80, Nr. 2, 2020, s. 147-165.

Publikation: Bidrag til tidsskriftReviewForskningfagfællebedømt

Harvard

Harris, S, Abrahamson, MJ, Ceriello, A, Charpentier, G, Evans, M, Lehmann, R, Liebl, A, Linjawi, S, Holt, RIG, Hosszúfalusi, N, Rutten, G & Vilsbøll, T 2020, 'Clinical Considerations When Initiating and Titrating Insulin Degludec/Liraglutide (IDegLira) in People with Type 2 Diabetes', Drugs, bind 80, nr. 2, s. 147-165. https://doi.org/10.1007/s40265-019-01245-3

APA

Harris, S., Abrahamson, M. J., Ceriello, A., Charpentier, G., Evans, M., Lehmann, R., Liebl, A., Linjawi, S., Holt, R. I. G., Hosszúfalusi, N., Rutten, G., & Vilsbøll, T. (2020). Clinical Considerations When Initiating and Titrating Insulin Degludec/Liraglutide (IDegLira) in People with Type 2 Diabetes. Drugs, 80(2), 147-165. https://doi.org/10.1007/s40265-019-01245-3

Vancouver

Harris S, Abrahamson MJ, Ceriello A, Charpentier G, Evans M, Lehmann R o.a. Clinical Considerations When Initiating and Titrating Insulin Degludec/Liraglutide (IDegLira) in People with Type 2 Diabetes. Drugs. 2020;80(2):147-165. https://doi.org/10.1007/s40265-019-01245-3

Author

Harris, Stewart ; Abrahamson, Martin J. ; Ceriello, Antonio ; Charpentier, Guillaume ; Evans, Marc ; Lehmann, Roger ; Liebl, Andreas ; Linjawi, Sultan ; Holt, Richard I.G. ; Hosszúfalusi, Nóra ; Rutten, Guy ; Vilsbøll, Tina. / Clinical Considerations When Initiating and Titrating Insulin Degludec/Liraglutide (IDegLira) in People with Type 2 Diabetes. I: Drugs. 2020 ; Bind 80, Nr. 2. s. 147-165.

Bibtex

@article{ff86a6dfa69240ba8468267d01e09d02,
title = "Clinical Considerations When Initiating and Titrating Insulin Degludec/Liraglutide (IDegLira) in People with Type 2 Diabetes",
abstract = "Therapeutic inertia is a substantial obstacle to the initiation of insulin therapy in people with uncontrolled type 2 diabetes (T2D). This effect has in part been perpetuated by concerns over the impact of a burdensome regimen and the increased risk of hypoglycemia and body weight gain often associated with insulin use. An effective, yet simple, less burdensome regimen with a lower risk of body weight gain and hypoglycemia compared with an insulin-only regimen, may help to address these concerns more effectively. We review the available clinical and real-world data on IDegLira, a once-daily, injectable, fixed-ratio combination of insulin degludec (degludec) and the glucagon-like peptide-1 receptor agonist (GLP-1RA) liraglutide, in people with T2D. Evidence from the comprehensive DUAL clinical trial program suggests an advantage of IDegLira over traditional insulin therapies in a number of clinical outcomes, including maintenance of glycemic control, achievement of glycemic targets, reducing the risk of hypoglycemia, and body weight loss. These findings were demonstrated in participants with T2D irrespective of prior GLP-1RA and insulin use. Furthermore, the individual components of IDegLira have confirmed safety (degludec) or significant benefit in terms of improvement of cardiovascular risk (liraglutide). As an injectable therapy that is simple to titrate, IDegLira has the potential to optimize the ability to achieve relevant glycemic targets, and offers a suitable treatment option for people with T2D requiring insulin therapy who are at risk of hypoglycemia or weight gain.",
author = "Stewart Harris and Abrahamson, {Martin J.} and Antonio Ceriello and Guillaume Charpentier and Marc Evans and Roger Lehmann and Andreas Liebl and Sultan Linjawi and Holt, {Richard I.G.} and N{\'o}ra Hossz{\'u}falusi and Guy Rutten and Tina Vilsb{\o}ll",
year = "2020",
doi = "10.1007/s40265-019-01245-3",
language = "English",
volume = "80",
pages = "147--165",
journal = "Drugs",
issn = "0012-6667",
publisher = "Adis International Ltd",
number = "2",

}

RIS

TY - JOUR

T1 - Clinical Considerations When Initiating and Titrating Insulin Degludec/Liraglutide (IDegLira) in People with Type 2 Diabetes

AU - Harris, Stewart

AU - Abrahamson, Martin J.

AU - Ceriello, Antonio

AU - Charpentier, Guillaume

AU - Evans, Marc

AU - Lehmann, Roger

AU - Liebl, Andreas

AU - Linjawi, Sultan

AU - Holt, Richard I.G.

AU - Hosszúfalusi, Nóra

AU - Rutten, Guy

AU - Vilsbøll, Tina

PY - 2020

Y1 - 2020

N2 - Therapeutic inertia is a substantial obstacle to the initiation of insulin therapy in people with uncontrolled type 2 diabetes (T2D). This effect has in part been perpetuated by concerns over the impact of a burdensome regimen and the increased risk of hypoglycemia and body weight gain often associated with insulin use. An effective, yet simple, less burdensome regimen with a lower risk of body weight gain and hypoglycemia compared with an insulin-only regimen, may help to address these concerns more effectively. We review the available clinical and real-world data on IDegLira, a once-daily, injectable, fixed-ratio combination of insulin degludec (degludec) and the glucagon-like peptide-1 receptor agonist (GLP-1RA) liraglutide, in people with T2D. Evidence from the comprehensive DUAL clinical trial program suggests an advantage of IDegLira over traditional insulin therapies in a number of clinical outcomes, including maintenance of glycemic control, achievement of glycemic targets, reducing the risk of hypoglycemia, and body weight loss. These findings were demonstrated in participants with T2D irrespective of prior GLP-1RA and insulin use. Furthermore, the individual components of IDegLira have confirmed safety (degludec) or significant benefit in terms of improvement of cardiovascular risk (liraglutide). As an injectable therapy that is simple to titrate, IDegLira has the potential to optimize the ability to achieve relevant glycemic targets, and offers a suitable treatment option for people with T2D requiring insulin therapy who are at risk of hypoglycemia or weight gain.

AB - Therapeutic inertia is a substantial obstacle to the initiation of insulin therapy in people with uncontrolled type 2 diabetes (T2D). This effect has in part been perpetuated by concerns over the impact of a burdensome regimen and the increased risk of hypoglycemia and body weight gain often associated with insulin use. An effective, yet simple, less burdensome regimen with a lower risk of body weight gain and hypoglycemia compared with an insulin-only regimen, may help to address these concerns more effectively. We review the available clinical and real-world data on IDegLira, a once-daily, injectable, fixed-ratio combination of insulin degludec (degludec) and the glucagon-like peptide-1 receptor agonist (GLP-1RA) liraglutide, in people with T2D. Evidence from the comprehensive DUAL clinical trial program suggests an advantage of IDegLira over traditional insulin therapies in a number of clinical outcomes, including maintenance of glycemic control, achievement of glycemic targets, reducing the risk of hypoglycemia, and body weight loss. These findings were demonstrated in participants with T2D irrespective of prior GLP-1RA and insulin use. Furthermore, the individual components of IDegLira have confirmed safety (degludec) or significant benefit in terms of improvement of cardiovascular risk (liraglutide). As an injectable therapy that is simple to titrate, IDegLira has the potential to optimize the ability to achieve relevant glycemic targets, and offers a suitable treatment option for people with T2D requiring insulin therapy who are at risk of hypoglycemia or weight gain.

UR - http://www.scopus.com/inward/record.url?scp=85078247530&partnerID=8YFLogxK

U2 - 10.1007/s40265-019-01245-3

DO - 10.1007/s40265-019-01245-3

M3 - Review

C2 - 31960258

AN - SCOPUS:85078247530

VL - 80

SP - 147

EP - 165

JO - Drugs

JF - Drugs

SN - 0012-6667

IS - 2

ER -

ID: 254520683