Year 2022 / Volume 114 / Number 2
Letter
Switch to subcutaneous infliximab during the SARS-CoV-2 pandemic: preliminary results

118-119

DOI: 10.17235/reed.2021.8320/2021

Federico Argüelles-Arias, Paula Fernández Álvarez, Luisa Castro Laria, Belén Maldonado Pérez, María Belvis Jiménez, Vicente Merino-Bohórquez, Ángel Caunedo Álvarez, Miguel Ángel Calleja Hernández,

Abstract
A new subcutaneous formulation of the infliximab biosimilar CT-P13 has recently been developed for the treatment of inflammatory bowel disease (IBD), providing response rates similar to intravenous treatment. The use of this new formulation was requested, in an effort to limit patient attendance at intravenous infusion centers and to maintain biological treatment during the COVID-19 pandemic. The objective of this observational, retrospective and descriptive study was to assess CT-P13 efficacy and safety after switching from intravenous to a subcutaneous formulation in patients with IBD receiving maintenance therapy. This article shows preliminary results after six months of follow-up.
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Citation tools
Argüelles-Arias F, Fernández Álvarez P, Castro Laria L, Maldonado Pérez B, Belvis Jiménez M, Merino-Bohórquez V, et all. Switch to subcutaneous infliximab during the SARS-CoV-2 pandemic: preliminary results. 8320/2021


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Publication history

Received: 01/09/2021

Accepted: 03/09/2021

Online First: 14/09/2021

Published: 07/02/2022

Article Online First time: 13 days

Article editing time: 159 days


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