Cargando…

Ten Years of Experience with Biphasic Insulin Aspart 30: From Drug Development to the Latest Clinical Findings

Biphasic insulin aspart 30 (BIAsp 30) includes 30% soluble rapid-acting insulin aspart (IAsp) along with an intermediate-acting 70% protaminated IAsp that provides coverage of prandial and basal insulin in a single injection. As BIAsp 30 has been available internationally for 10 years, this review p...

Descripción completa

Detalles Bibliográficos
Autores principales: Liebl, Andreas, Prusty, Vinay, Valensi, Paul, Kawamori, Ryuzo, Christiansen, Jens Sandahl, Palmer, Andrew J., Balschmidt, Per, Ligthelm, Robert, Mohan, Viswanathan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3590411/
https://www.ncbi.nlm.nih.gov/pubmed/22818015
http://dx.doi.org/10.2165/11635490-000000000-00000
_version_ 1782261856121913344
author Liebl, Andreas
Prusty, Vinay
Valensi, Paul
Kawamori, Ryuzo
Christiansen, Jens Sandahl
Palmer, Andrew J.
Balschmidt, Per
Ligthelm, Robert
Mohan, Viswanathan
author_facet Liebl, Andreas
Prusty, Vinay
Valensi, Paul
Kawamori, Ryuzo
Christiansen, Jens Sandahl
Palmer, Andrew J.
Balschmidt, Per
Ligthelm, Robert
Mohan, Viswanathan
author_sort Liebl, Andreas
collection PubMed
description Biphasic insulin aspart 30 (BIAsp 30) includes 30% soluble rapid-acting insulin aspart (IAsp) along with an intermediate-acting 70% protaminated IAsp that provides coverage of prandial and basal insulin in a single injection. As BIAsp 30 has been available internationally for 10 years, this review provides a comprehensive overview of the discovery of BIAsp 30, its pharmacokinetic and pharmacodynamic profile, safety and efficacy outcomes from the clinical trial programme, ‘real-life’ clinical insights provided by observational study data, and cost effectiveness and quality-of-life information. These studies have demonstrated that BIAsp 30 once or twice daily is an appropriate option for insulin initiation. BIAsp 30 also provides a switch option in patients on biphasic human insulin (BHI). Switching from BHI to BIAsp 30 is associated with improved postprandial glucose (PPG) and reduced nocturnal and major hypoglycaemia, although daytime hypoglycaemia is higher with BIAsp 30. Intensification of BIAsp 30 can be achieved by increasing the number of daily doses up to three times daily with meals. Therefore, BIAsp 30 provides an intensification option for individuals who are not achieving control with basal insulin and would prefer the simplicity of a single biphasic insulin instead of progressing to a basal-bolus approach. BIAsp 30 has a simple dose-titration algorithm, which enables patients to effectively self-titrate their insulin dose. Cost-effectiveness analyses have demonstrated that BIAsp 30 is cost effective or dominant compared with BHI 30 or insulin glargine in a number of healthcare settings. In conclusion, BIAsp 30 offers a simple and flexible option for insulin initiation and intensification that provides coverage of both fasting and prandial glucose.
format Online
Article
Text
id pubmed-3590411
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher Springer International Publishing
record_format MEDLINE/PubMed
spelling pubmed-35904112013-03-07 Ten Years of Experience with Biphasic Insulin Aspart 30: From Drug Development to the Latest Clinical Findings Liebl, Andreas Prusty, Vinay Valensi, Paul Kawamori, Ryuzo Christiansen, Jens Sandahl Palmer, Andrew J. Balschmidt, Per Ligthelm, Robert Mohan, Viswanathan Drugs Review Article Biphasic insulin aspart 30 (BIAsp 30) includes 30% soluble rapid-acting insulin aspart (IAsp) along with an intermediate-acting 70% protaminated IAsp that provides coverage of prandial and basal insulin in a single injection. As BIAsp 30 has been available internationally for 10 years, this review provides a comprehensive overview of the discovery of BIAsp 30, its pharmacokinetic and pharmacodynamic profile, safety and efficacy outcomes from the clinical trial programme, ‘real-life’ clinical insights provided by observational study data, and cost effectiveness and quality-of-life information. These studies have demonstrated that BIAsp 30 once or twice daily is an appropriate option for insulin initiation. BIAsp 30 also provides a switch option in patients on biphasic human insulin (BHI). Switching from BHI to BIAsp 30 is associated with improved postprandial glucose (PPG) and reduced nocturnal and major hypoglycaemia, although daytime hypoglycaemia is higher with BIAsp 30. Intensification of BIAsp 30 can be achieved by increasing the number of daily doses up to three times daily with meals. Therefore, BIAsp 30 provides an intensification option for individuals who are not achieving control with basal insulin and would prefer the simplicity of a single biphasic insulin instead of progressing to a basal-bolus approach. BIAsp 30 has a simple dose-titration algorithm, which enables patients to effectively self-titrate their insulin dose. Cost-effectiveness analyses have demonstrated that BIAsp 30 is cost effective or dominant compared with BHI 30 or insulin glargine in a number of healthcare settings. In conclusion, BIAsp 30 offers a simple and flexible option for insulin initiation and intensification that provides coverage of both fasting and prandial glucose. Springer International Publishing 2012-01-06 2012-07 /pmc/articles/PMC3590411/ /pubmed/22818015 http://dx.doi.org/10.2165/11635490-000000000-00000 Text en © Springer International Publishing AG 2012
spellingShingle Review Article
Liebl, Andreas
Prusty, Vinay
Valensi, Paul
Kawamori, Ryuzo
Christiansen, Jens Sandahl
Palmer, Andrew J.
Balschmidt, Per
Ligthelm, Robert
Mohan, Viswanathan
Ten Years of Experience with Biphasic Insulin Aspart 30: From Drug Development to the Latest Clinical Findings
title Ten Years of Experience with Biphasic Insulin Aspart 30: From Drug Development to the Latest Clinical Findings
title_full Ten Years of Experience with Biphasic Insulin Aspart 30: From Drug Development to the Latest Clinical Findings
title_fullStr Ten Years of Experience with Biphasic Insulin Aspart 30: From Drug Development to the Latest Clinical Findings
title_full_unstemmed Ten Years of Experience with Biphasic Insulin Aspart 30: From Drug Development to the Latest Clinical Findings
title_short Ten Years of Experience with Biphasic Insulin Aspart 30: From Drug Development to the Latest Clinical Findings
title_sort ten years of experience with biphasic insulin aspart 30: from drug development to the latest clinical findings
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3590411/
https://www.ncbi.nlm.nih.gov/pubmed/22818015
http://dx.doi.org/10.2165/11635490-000000000-00000
work_keys_str_mv AT lieblandreas tenyearsofexperiencewithbiphasicinsulinaspart30fromdrugdevelopmenttothelatestclinicalfindings
AT prustyvinay tenyearsofexperiencewithbiphasicinsulinaspart30fromdrugdevelopmenttothelatestclinicalfindings
AT valensipaul tenyearsofexperiencewithbiphasicinsulinaspart30fromdrugdevelopmenttothelatestclinicalfindings
AT kawamoriryuzo tenyearsofexperiencewithbiphasicinsulinaspart30fromdrugdevelopmenttothelatestclinicalfindings
AT christiansenjenssandahl tenyearsofexperiencewithbiphasicinsulinaspart30fromdrugdevelopmenttothelatestclinicalfindings
AT palmerandrewj tenyearsofexperiencewithbiphasicinsulinaspart30fromdrugdevelopmenttothelatestclinicalfindings
AT balschmidtper tenyearsofexperiencewithbiphasicinsulinaspart30fromdrugdevelopmenttothelatestclinicalfindings
AT ligthelmrobert tenyearsofexperiencewithbiphasicinsulinaspart30fromdrugdevelopmenttothelatestclinicalfindings
AT mohanviswanathan tenyearsofexperiencewithbiphasicinsulinaspart30fromdrugdevelopmenttothelatestclinicalfindings