British Society of Gastroenterology consensus guidelines on the management of inflammatory bowel disease in adults

CA Lamb, NA Kennedy, T Raine, PA Hendy, PJ Smith… - Gut, 2019 - gut.bmj.com
Ulcerative colitis and Crohn's disease are the principal forms of inflammatory bowel disease.
Both represent chronic inflammation of the gastrointestinal tract, which displays …

[HTML][HTML] Switching reference medicines to biosimilars: a systematic literature review of clinical outcomes

HP Cohen, A Blauvelt, RM Rifkin, S Danese… - Drugs, 2018 - Springer
Methods A systematic search was conducted using the Medline® and Embase® databases
up to 30 June 2017 employing specific medical subject heading terms. Additionally, the …

Switching from originator infliximab to biosimilar CT-P13 compared with maintained treatment with originator infliximab (NOR-SWITCH): a 52-week, randomised …

KK Jørgensen, IC Olsen, GL Goll, M Lorentzen… - The Lancet, 2017 - thelancet.com
Background TNF inhibitors have improved treatment of Crohn's disease, ulcerative colitis,
spondyloarthritis, rheumatoid arthritis, psoriatic arthritis, and chronic plaque psoriasis, but …

Efficacy and safety of CT-P13 (biosimilar infliximab) in patients with rheumatoid arthritis: comparison between switching from reference infliximab to CT-P13 and …

DH Yoo, N Prodanovic, J Jaworski, P Miranda… - Annals of the …, 2017 - ard.bmj.com
Objectives To assess the efficacy and safety of switching from the infliximab reference
product (RP; Remicade) to its biosimilar CT-P13 (Remsima, Inflectra) or continuing CT-P13 …

ECCO position statement on the use of biosimilars for inflammatory bowel disease—an update

S Danese, G Fiorino, T Raine, M Ferrante… - Journal of Crohn's …, 2017 - academic.oup.com
Biosimilars of infliximab were first approved by the European Medicine Agency in 2013, 1, 2
based on pre-clinical studies on biosimilarity and on clinical data coming from two …

A nationwide non-medical switch from originator infliximab to biosimilar CT-P13 in 802 patients with inflammatory arthritis: 1-year clinical outcomes from the DANBIO …

B Glintborg, IJ Sørensen, AG Loft… - Annals of the …, 2017 - ard.bmj.com
Objectives According to guidelines, a nationwide non-medical switch from originator (INX,
Remicade) to biosimilar infliximab (Remsima, CT-P13) was conducted in Danish patients …

The efficacy, safety, and immunogenicity of switching between reference biopharmaceuticals and biosimilars: a systematic review

L Barbier, HC Ebbers, P Declerck… - Clinical …, 2020 - Wiley Online Library
To date, no consensus exists among stakeholders about switching patients between
reference biological products (RPs) and biosimilars, which may have been curbing the …

Consensus-based recommendations for the use of biosimilars to treat rheumatological diseases

J Kay, MM Schoels, T Dörner, P Emery… - Annals of the …, 2018 - ard.bmj.com
The study aimed to develop evidence-based recommendations regarding the evaluation
and use of biosimilars to treat rheumatological diseases. The task force comprised an expert …

Efficacy and safety of biological DMARDs: a systematic literature review informing the 2022 update of the ASAS-EULAR recommendations for the management of …

C Webers, A Ortolan, A Sepriano, L Falzon… - Annals of the …, 2023 - ard.bmj.com
Objective To update the evidence on efficacy and safety of biological disease-modifying
antirheumatic drugs (bDMARDs) in patients with axial spondyloarthritis (axSpA) to inform the …

Safety, immunogenicity and interchangeability of biosimilar monoclonal antibodies and fusion proteins: a regulatory perspective

P Kurki, S Barry, I Bourges, P Tsantili, E Wolff-Holz - Drugs, 2021 - Springer
Background Biosimilars have been used for 15 years in the European Union (EU), and have
been shown to reduce costs and increase access to important biological medicines. In spite …