Biosimilar-to-Biosimilar Switching in Routine Care – Results on >1,600 Patients with Inflammatory Arthritis in the DANBIO Registry

Hafsah Nabi, Oliver Hendricks, Dorte Vendelbo Jensen, Anne Gitte Loft, Jens Pedersen, Søren Andreas Just, Kamilla Danebod, Heidi Lausten Munk, Salome Kristensen, Natalia Manilo, Ada Colic, Asta Linauskas, Pia Høger Thygesen, Louise Christensen, Maren Høgberget Kalisz, Niels Lomborg, Stavros Chrysidis, Johnny Lillelund Raun, Marlene Andersen, Frank MehnertNiels Steen Krogh, Merete Lund Hetland, Bente Glintborg

Abstract

Background/Purpose:
In routine care, biosimilar-to-biosimilar infliximab switching may occur to save costs (=non-medical switching). Previous studies have investigated the efficacy and safety of switches from originator infliximab to corresponding biosimilar in patients with inflammatory rheumatic diseases (1). However, the outcomes after switching from one infliximab biosimilar to a second infliximab biosimilar remain scarcely investigated. Denmark has recently conducted a nationwide mandatory infliximab biosimilar-to-biosimilar switch. In this study, we aimed to investigate the effectiveness of switching infliximab biosimilars CT-P13-to-GP1111 among patients with rheumatoid arthritis (RA), psoriatic arthritis (PsA) and axial spondyloarthritis (AxSpA), including patients who had previously switched from originator (originator-experienced) to CT-P13 as well as patients who were originator-naïve.
OriginalsprogEngelsk
Publikationsdato2022
StatusUdgivet - 2022
BegivenhedACR 2022 - Philadelphia
Varighed: 10 nov. 202214 nov. 2022

Konference

KonferenceACR 2022
ByPhiladelphia
Periode10/11/202214/11/2022

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