British Society of Gastroenterology consensus guidelines on the management of inflammatory bowel disease in adults
Ulcerative colitis and Crohn's disease are the principal forms of inflammatory bowel disease.
Both represent chronic inflammation of the gastrointestinal tract, which displays …
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 …
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 …
Background TNF inhibitors have improved treatment of Crohn's disease, ulcerative colitis,
spondyloarthritis, rheumatoid arthritis, psoriatic arthritis, and chronic plaque psoriasis, but …
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 …
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
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 …
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 …
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
To date, no consensus exists among stakeholders about switching patients between
reference biological products (RPs) and biosimilars, which may have been curbing the …
reference biological products (RPs) and biosimilars, which may have been curbing the …
Consensus-based recommendations for the use of biosimilars to treat rheumatological diseases
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 …
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 …
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 …
been shown to reduce costs and increase access to important biological medicines. In spite …