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Molecular and pharmacological characterization of insulin icodec: a new basal insulin analog designed for once-weekly dosing
INTRODUCTION: Insulin icodec is a novel, long-acting insulin analog designed to cover basal insulin requirements with once-weekly subcutaneous administration. Here we describe the molecular engineering and the biological and pharmacological properties of insulin icodec. RESEARCH DESIGN AND METHODS:...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8378355/ https://www.ncbi.nlm.nih.gov/pubmed/34413118 http://dx.doi.org/10.1136/bmjdrc-2021-002301 |
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author | Nishimura, Erica Pridal, Lone Glendorf, Tine Hansen, Bo Falk Hubálek, František Kjeldsen, Thomas Kristensen, Niels Rode Lützen, Anne Lyby, Karsten Madsen, Peter Pedersen, Thomas Åskov Ribel-Madsen, Rasmus Stidsen, Carsten Enggaard Haahr, Hanne |
author_facet | Nishimura, Erica Pridal, Lone Glendorf, Tine Hansen, Bo Falk Hubálek, František Kjeldsen, Thomas Kristensen, Niels Rode Lützen, Anne Lyby, Karsten Madsen, Peter Pedersen, Thomas Åskov Ribel-Madsen, Rasmus Stidsen, Carsten Enggaard Haahr, Hanne |
author_sort | Nishimura, Erica |
collection | PubMed |
description | INTRODUCTION: Insulin icodec is a novel, long-acting insulin analog designed to cover basal insulin requirements with once-weekly subcutaneous administration. Here we describe the molecular engineering and the biological and pharmacological properties of insulin icodec. RESEARCH DESIGN AND METHODS: A number of in vitro assays measuring receptor binding, intracellular signaling as well as cellular metabolic and mitogenic responses were used to characterize the biological properties of insulin icodec. To evaluate the pharmacological properties of insulin icodec in individuals with type 2 diabetes, a randomized, double-blind, double-dummy, active-controlled, multiple-dose, dose escalation trial was conducted. RESULTS: The long half-life of insulin icodec was achieved by introducing modifications to the insulin molecule aiming to obtain a safe, albumin-bound circulating depot of insulin icodec, providing protracted insulin action and clearance. Addition of a C20 fatty diacid-containing side chain imparts strong, reversible albumin binding, while three amino acid substitutions (A14E, B16H and B25H) provide molecular stability and contribute to attenuating insulin receptor (IR) binding and clearance, further prolonging the half-life. In vitro cell-based studies showed that insulin icodec activates the same dose-dependent IR-mediated signaling and metabolic responses as native human insulin (HI). The affinity of insulin icodec for the insulin-like growth factor-1 receptor was proportionately lower than its binding to the IR, and the in vitro mitogenic effect of insulin icodec in various human cells was low relative to HI. The clinical pharmacology trial in people with type 2 diabetes showed that insulin icodec was well tolerated and has pharmacokinetic/pharmacodynamic properties that are suited for once-weekly dosing, with a mean half-life of 196 hours and close to even distribution of glucose-lowering effect over the entire dosing interval of 1 week. CONCLUSIONS: The molecular modifications introduced into insulin icodec provide a novel basal insulin with biological and pharmacokinetic/pharmacodynamic properties suitable for once-weekly dosing. TRIAL REGISTRATION NUMBER: NCT02964104. |
format | Online Article Text |
id | pubmed-8378355 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-83783552021-09-02 Molecular and pharmacological characterization of insulin icodec: a new basal insulin analog designed for once-weekly dosing Nishimura, Erica Pridal, Lone Glendorf, Tine Hansen, Bo Falk Hubálek, František Kjeldsen, Thomas Kristensen, Niels Rode Lützen, Anne Lyby, Karsten Madsen, Peter Pedersen, Thomas Åskov Ribel-Madsen, Rasmus Stidsen, Carsten Enggaard Haahr, Hanne BMJ Open Diabetes Res Care Emerging Technologies, Pharmacology and Therapeutics INTRODUCTION: Insulin icodec is a novel, long-acting insulin analog designed to cover basal insulin requirements with once-weekly subcutaneous administration. Here we describe the molecular engineering and the biological and pharmacological properties of insulin icodec. RESEARCH DESIGN AND METHODS: A number of in vitro assays measuring receptor binding, intracellular signaling as well as cellular metabolic and mitogenic responses were used to characterize the biological properties of insulin icodec. To evaluate the pharmacological properties of insulin icodec in individuals with type 2 diabetes, a randomized, double-blind, double-dummy, active-controlled, multiple-dose, dose escalation trial was conducted. RESULTS: The long half-life of insulin icodec was achieved by introducing modifications to the insulin molecule aiming to obtain a safe, albumin-bound circulating depot of insulin icodec, providing protracted insulin action and clearance. Addition of a C20 fatty diacid-containing side chain imparts strong, reversible albumin binding, while three amino acid substitutions (A14E, B16H and B25H) provide molecular stability and contribute to attenuating insulin receptor (IR) binding and clearance, further prolonging the half-life. In vitro cell-based studies showed that insulin icodec activates the same dose-dependent IR-mediated signaling and metabolic responses as native human insulin (HI). The affinity of insulin icodec for the insulin-like growth factor-1 receptor was proportionately lower than its binding to the IR, and the in vitro mitogenic effect of insulin icodec in various human cells was low relative to HI. The clinical pharmacology trial in people with type 2 diabetes showed that insulin icodec was well tolerated and has pharmacokinetic/pharmacodynamic properties that are suited for once-weekly dosing, with a mean half-life of 196 hours and close to even distribution of glucose-lowering effect over the entire dosing interval of 1 week. CONCLUSIONS: The molecular modifications introduced into insulin icodec provide a novel basal insulin with biological and pharmacokinetic/pharmacodynamic properties suitable for once-weekly dosing. TRIAL REGISTRATION NUMBER: NCT02964104. BMJ Publishing Group 2021-08-19 /pmc/articles/PMC8378355/ /pubmed/34413118 http://dx.doi.org/10.1136/bmjdrc-2021-002301 Text en © Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) . |
spellingShingle | Emerging Technologies, Pharmacology and Therapeutics Nishimura, Erica Pridal, Lone Glendorf, Tine Hansen, Bo Falk Hubálek, František Kjeldsen, Thomas Kristensen, Niels Rode Lützen, Anne Lyby, Karsten Madsen, Peter Pedersen, Thomas Åskov Ribel-Madsen, Rasmus Stidsen, Carsten Enggaard Haahr, Hanne Molecular and pharmacological characterization of insulin icodec: a new basal insulin analog designed for once-weekly dosing |
title | Molecular and pharmacological characterization of insulin icodec: a new basal insulin analog designed for once-weekly dosing |
title_full | Molecular and pharmacological characterization of insulin icodec: a new basal insulin analog designed for once-weekly dosing |
title_fullStr | Molecular and pharmacological characterization of insulin icodec: a new basal insulin analog designed for once-weekly dosing |
title_full_unstemmed | Molecular and pharmacological characterization of insulin icodec: a new basal insulin analog designed for once-weekly dosing |
title_short | Molecular and pharmacological characterization of insulin icodec: a new basal insulin analog designed for once-weekly dosing |
title_sort | molecular and pharmacological characterization of insulin icodec: a new basal insulin analog designed for once-weekly dosing |
topic | Emerging Technologies, Pharmacology and Therapeutics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8378355/ https://www.ncbi.nlm.nih.gov/pubmed/34413118 http://dx.doi.org/10.1136/bmjdrc-2021-002301 |
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