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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.
Vermeire, Séverine; D'heygere, François; Nakad, Antoine; Franchimont, Denis; Fontaine, Fernand; Louis, Edouard; Van Hootegem, Philippe; Dewit, Olivier; Lambrecht, Guy; Strubbe, Beatrijs; Baert, Filip.
  • Vermeire S; Department of Gastroenterology, University Hospital Gasthuisberg, Leuven, Belgium, severine.vermeire@uzleuven.be.
  • D'heygere F; Department of Gastroenterology, AZ Groeninge, Kortrijk, Belgium.
  • Nakad A; Department of Gastroenterology, CHWAPI, Tournai, Belgium.
  • Franchimont D; Department of Gastroenterology, Erasme Hospital, Brussels, Belgium.
  • Fontaine F; Department of Gastroenterology, CHC St Joseph, Liège, Belgium.
  • Louis E; Department of Gastroenterology, University Hospital CHU Sart Tilman, Liège, Belgium.
  • Van Hootegem P; Department of Gastroenterology, AZ St Lucas, Brugge, Belgium.
  • Dewit O; Department of Gastroenterology, UCL St Luc, Brussels, Belgium.
  • Lambrecht G; Department of Gastroenterology, AZ Damiaan, Oostende, Belgium.
  • Strubbe B; Department of Gastroenterology, OLV Hospital, Aalst, Belgium.
  • Baert F; Department of Gastroenterology, AZ Delta, Roeselare-Menen, Belgium.
Patient Prefer Adherence ; 12: 1193-1202, 2018.
Article en En | MEDLINE | ID: mdl-30013330
ABSTRACT

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 11 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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Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Clinical_trials Idioma: En Año: 2018 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Clinical_trials Idioma: En Año: 2018 Tipo del documento: Article