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The Effect of Food Intake on the Pharmacokinetics of Oral Basal Insulin: A Randomised Crossover Trial in Healthy Male Subjects

BACKGROUND: Oral insulin 338 is a novel tablet formulation of a long-acting basal insulin. This randomised, open-label, four-period crossover trial investigated the effect of timing of food intake on the single-dose pharmacokinetic properties of oral insulin 338. METHODS: After an overnight fast, 44...

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Autores principales: Halberg, Inge B., Lyby, Karsten, Wassermann, Karsten, Heise, Tim, Plum-Mörschel, Leona, Zijlstra, Eric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6856260/
https://www.ncbi.nlm.nih.gov/pubmed/31093929
http://dx.doi.org/10.1007/s40262-019-00772-2
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author Halberg, Inge B.
Lyby, Karsten
Wassermann, Karsten
Heise, Tim
Plum-Mörschel, Leona
Zijlstra, Eric
author_facet Halberg, Inge B.
Lyby, Karsten
Wassermann, Karsten
Heise, Tim
Plum-Mörschel, Leona
Zijlstra, Eric
author_sort Halberg, Inge B.
collection PubMed
description BACKGROUND: Oral insulin 338 is a novel tablet formulation of a long-acting basal insulin. This randomised, open-label, four-period crossover trial investigated the effect of timing of food intake on the single-dose pharmacokinetic properties of oral insulin 338. METHODS: After an overnight fast, 44 healthy males received single fixed doses of oral insulin 338 administered 0, 30, 60 or 360 min before consuming a standardised meal (500 kcal, 57 energy percent [E%] carbohydrate, 13 E% fat, 30 E% protein). Blood samples for pharmacokinetic assessment were taken up to 288 h post-dose. RESULTS: Total exposure (area under the concentration-time curve from time zero to infinity [AUC(Ins338,0–∞)]) and maximum concentration (C(max,Ins338)) of insulin 338 were both significantly lower for 0 versus 360 min post-dose fasting (ratio [95% confidence interval (CI)]: 0.36 [0.26–0.49], p < 0.001, and 0.35 [0.25–0.49], p < 0.001, respectively). There were no significant differences in AUC(Ins338,0–∞) and C(max,Ins338) for 30 or 60 versus 360 min post-dose fasting (ratio [95% CI] 30 versus 360 min: 0.85 [0.61–1.21], p = 0.36, and 0.86 [0.59–1.26], p = 0.42; ratio [95% CI] 60 versus 360 min: 0.96 [0.72–1.28], p = 0.77, and 0.99 [0.75–1.31], p = 0.95). The mean half-life was ~ 55 h independent of the post-dose fasting period. Oral insulin 338 was well-tolerated with no safety issues identified during the trial. CONCLUSIONS: Oral insulin 338 pharmacokinetics are not affected by food intake from 30 min after dosing, implying that patients with diabetes mellitus do not need to wait more than 30 min after a morning dose of oral insulin 338 before having their breakfast. This is considered important for convenience and treatment compliance. CLINICALTRIALS.GOV IDENTIFIER: NCT02304627. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s40262-019-00772-2) contains supplementary material, which is available to authorized users.
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spelling pubmed-68562602019-12-03 The Effect of Food Intake on the Pharmacokinetics of Oral Basal Insulin: A Randomised Crossover Trial in Healthy Male Subjects Halberg, Inge B. Lyby, Karsten Wassermann, Karsten Heise, Tim Plum-Mörschel, Leona Zijlstra, Eric Clin Pharmacokinet Original Research Article BACKGROUND: Oral insulin 338 is a novel tablet formulation of a long-acting basal insulin. This randomised, open-label, four-period crossover trial investigated the effect of timing of food intake on the single-dose pharmacokinetic properties of oral insulin 338. METHODS: After an overnight fast, 44 healthy males received single fixed doses of oral insulin 338 administered 0, 30, 60 or 360 min before consuming a standardised meal (500 kcal, 57 energy percent [E%] carbohydrate, 13 E% fat, 30 E% protein). Blood samples for pharmacokinetic assessment were taken up to 288 h post-dose. RESULTS: Total exposure (area under the concentration-time curve from time zero to infinity [AUC(Ins338,0–∞)]) and maximum concentration (C(max,Ins338)) of insulin 338 were both significantly lower for 0 versus 360 min post-dose fasting (ratio [95% confidence interval (CI)]: 0.36 [0.26–0.49], p < 0.001, and 0.35 [0.25–0.49], p < 0.001, respectively). There were no significant differences in AUC(Ins338,0–∞) and C(max,Ins338) for 30 or 60 versus 360 min post-dose fasting (ratio [95% CI] 30 versus 360 min: 0.85 [0.61–1.21], p = 0.36, and 0.86 [0.59–1.26], p = 0.42; ratio [95% CI] 60 versus 360 min: 0.96 [0.72–1.28], p = 0.77, and 0.99 [0.75–1.31], p = 0.95). The mean half-life was ~ 55 h independent of the post-dose fasting period. Oral insulin 338 was well-tolerated with no safety issues identified during the trial. CONCLUSIONS: Oral insulin 338 pharmacokinetics are not affected by food intake from 30 min after dosing, implying that patients with diabetes mellitus do not need to wait more than 30 min after a morning dose of oral insulin 338 before having their breakfast. This is considered important for convenience and treatment compliance. CLINICALTRIALS.GOV IDENTIFIER: NCT02304627. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s40262-019-00772-2) contains supplementary material, which is available to authorized users. Springer International Publishing 2019-05-16 2019 /pmc/articles/PMC6856260/ /pubmed/31093929 http://dx.doi.org/10.1007/s40262-019-00772-2 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/), which permits any noncommercial use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Research Article
Halberg, Inge B.
Lyby, Karsten
Wassermann, Karsten
Heise, Tim
Plum-Mörschel, Leona
Zijlstra, Eric
The Effect of Food Intake on the Pharmacokinetics of Oral Basal Insulin: A Randomised Crossover Trial in Healthy Male Subjects
title The Effect of Food Intake on the Pharmacokinetics of Oral Basal Insulin: A Randomised Crossover Trial in Healthy Male Subjects
title_full The Effect of Food Intake on the Pharmacokinetics of Oral Basal Insulin: A Randomised Crossover Trial in Healthy Male Subjects
title_fullStr The Effect of Food Intake on the Pharmacokinetics of Oral Basal Insulin: A Randomised Crossover Trial in Healthy Male Subjects
title_full_unstemmed The Effect of Food Intake on the Pharmacokinetics of Oral Basal Insulin: A Randomised Crossover Trial in Healthy Male Subjects
title_short The Effect of Food Intake on the Pharmacokinetics of Oral Basal Insulin: A Randomised Crossover Trial in Healthy Male Subjects
title_sort effect of food intake on the pharmacokinetics of oral basal insulin: a randomised crossover trial in healthy male subjects
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6856260/
https://www.ncbi.nlm.nih.gov/pubmed/31093929
http://dx.doi.org/10.1007/s40262-019-00772-2
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