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Preference for a prefilled syringe or an auto-injection device for delivering golimumab in patients with moderate-to-severe ulcerative colitis: a randomized crossover study

PURPOSE: Simponi(®) (golimumab, MSD) is a fully human monoclonal antibody against tumor necrosis factor alpha administered subcutaneously using an autoinjector or a prefilled syringe. This study examined preference for administration of golimumab by autoinjector or prefilled syringe in patients with...

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Autores principales: Vermeire, Séverine, D’heygere, François, Nakad, Antoine, Franchimont, Denis, Fontaine, Fernand, Louis, Edouard, Van Hootegem, Philippe, Dewit, Olivier, Lambrecht, Guy, Strubbe, Beatrijs, Baert, Filip
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6039065/
https://www.ncbi.nlm.nih.gov/pubmed/30013330
http://dx.doi.org/10.2147/PPA.S154181
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author Vermeire, Séverine
D’heygere, François
Nakad, Antoine
Franchimont, Denis
Fontaine, Fernand
Louis, Edouard
Van Hootegem, Philippe
Dewit, Olivier
Lambrecht, Guy
Strubbe, Beatrijs
Baert, Filip
author_facet Vermeire, Séverine
D’heygere, François
Nakad, Antoine
Franchimont, Denis
Fontaine, Fernand
Louis, Edouard
Van Hootegem, Philippe
Dewit, Olivier
Lambrecht, Guy
Strubbe, Beatrijs
Baert, Filip
author_sort Vermeire, Séverine
collection PubMed
description PURPOSE: Simponi(®) (golimumab, MSD) is a fully human monoclonal antibody against tumor necrosis factor alpha administered subcutaneously using an autoinjector or a prefilled syringe. This study examined preference for administration of golimumab by autoinjector or prefilled syringe in patients with moderate-to-severe ulcerative colitis (UC). PATIENTS AND METHODS: This was a multicenter, open-label, randomized crossover trial (EudraCT no 2014-000656-29). Patients with moderate-to-severe UC were randomized 1:1 to receive 2 subcutaneous injections of 50 mg golimumab with the autoinjector followed by 2 injections of 50 mg with the prefilled syringe or the same 4 injections administered in the opposite order. Patients assessed preference, ease of use, and discomfort immediately after the injections and 2 weeks later. RESULTS: Ninety-one patients were included (median age=42.7 years [range, 19.7–93.7]; 58% male). The autoinjector was preferred by 76.9% of patients immediately after injections and by 71.4% 2 weeks later. The autoinjector was more often considered extremely easy or easy to use (94.5%) than the prefilled syringe (73.6%). Moderate discomfort or worse was reported by more patients when using the prefilled syringe (20.9%) than when using the autoinjector (5.5%), and severe discomfort or discomfort preventing injection of future doses was reported by 8.8% for the pre-filled syringe but not at all when using the autoinjector. A favorable or extremely favorable overall impression was reported by 89.0% for the autoinjector and 72.5% for the prefilled syringe. CONCLUSION: Most patients with moderate-to-severe UC preferred to self-administer golimumab with the autoinjector over a prefilled syringe.
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spelling pubmed-60390652018-07-16 Preference for a prefilled syringe or an auto-injection device for delivering golimumab in patients with moderate-to-severe ulcerative colitis: a randomized crossover study Vermeire, Séverine D’heygere, François Nakad, Antoine Franchimont, Denis Fontaine, Fernand Louis, Edouard Van Hootegem, Philippe Dewit, Olivier Lambrecht, Guy Strubbe, Beatrijs Baert, Filip Patient Prefer Adherence Original Research PURPOSE: Simponi(®) (golimumab, MSD) is a fully human monoclonal antibody against tumor necrosis factor alpha administered subcutaneously using an autoinjector or a prefilled syringe. This study examined preference for administration of golimumab by autoinjector or prefilled syringe in patients with moderate-to-severe ulcerative colitis (UC). PATIENTS AND METHODS: This was a multicenter, open-label, randomized crossover trial (EudraCT no 2014-000656-29). Patients with moderate-to-severe UC were randomized 1:1 to receive 2 subcutaneous injections of 50 mg golimumab with the autoinjector followed by 2 injections of 50 mg with the prefilled syringe or the same 4 injections administered in the opposite order. Patients assessed preference, ease of use, and discomfort immediately after the injections and 2 weeks later. RESULTS: Ninety-one patients were included (median age=42.7 years [range, 19.7–93.7]; 58% male). The autoinjector was preferred by 76.9% of patients immediately after injections and by 71.4% 2 weeks later. The autoinjector was more often considered extremely easy or easy to use (94.5%) than the prefilled syringe (73.6%). Moderate discomfort or worse was reported by more patients when using the prefilled syringe (20.9%) than when using the autoinjector (5.5%), and severe discomfort or discomfort preventing injection of future doses was reported by 8.8% for the pre-filled syringe but not at all when using the autoinjector. A favorable or extremely favorable overall impression was reported by 89.0% for the autoinjector and 72.5% for the prefilled syringe. CONCLUSION: Most patients with moderate-to-severe UC preferred to self-administer golimumab with the autoinjector over a prefilled syringe. Dove Medical Press 2018-07-06 /pmc/articles/PMC6039065/ /pubmed/30013330 http://dx.doi.org/10.2147/PPA.S154181 Text en © 2018 Vermeire et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Vermeire, Séverine
D’heygere, François
Nakad, Antoine
Franchimont, Denis
Fontaine, Fernand
Louis, Edouard
Van Hootegem, Philippe
Dewit, Olivier
Lambrecht, Guy
Strubbe, Beatrijs
Baert, Filip
Preference for a prefilled syringe or an auto-injection device for delivering golimumab in patients with moderate-to-severe ulcerative colitis: a randomized crossover study
title Preference for a prefilled syringe or an auto-injection device for delivering golimumab in patients with moderate-to-severe ulcerative colitis: a randomized crossover study
title_full Preference for a prefilled syringe or an auto-injection device for delivering golimumab in patients with moderate-to-severe ulcerative colitis: a randomized crossover study
title_fullStr Preference for a prefilled syringe or an auto-injection device for delivering golimumab in patients with moderate-to-severe ulcerative colitis: a randomized crossover study
title_full_unstemmed Preference for a prefilled syringe or an auto-injection device for delivering golimumab in patients with moderate-to-severe ulcerative colitis: a randomized crossover study
title_short Preference for a prefilled syringe or an auto-injection device for delivering golimumab in patients with moderate-to-severe ulcerative colitis: a randomized crossover study
title_sort preference for a prefilled syringe or an auto-injection device for delivering golimumab in patients with moderate-to-severe ulcerative colitis: a randomized crossover study
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6039065/
https://www.ncbi.nlm.nih.gov/pubmed/30013330
http://dx.doi.org/10.2147/PPA.S154181
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