Results 151 to 160 of about 8,557 (171)
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CT-P13 Subcutaneous Infliximab in Gastroenterology and Rheumatology
Immunotherapy, 2021The drug infliximab has been a key milestone in the treatment of inflammatory conditions such as Crohn's disease, ulcerative colitis, rheumatoid arthritis and the seronegative spondyloarthritides. Biosimilar drugs followed the originator, further improving access and diversity of therapy choice.
Mai Ahmed +3 more
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CT-P13 SC for the treatment of rheumatoid arthritis
Expert Review of Clinical Immunology, 2021Management of Rheumatoid Arthritis (RA) has improved following the implementation of early intensive treat to target recommendations and the availability of different biologicals. Most experience is with TNF blockers, but challenges remain in the efficacy/safety balance, immunogenicity, and long-term drug survival as well as availability and ...
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Comparison of the Pharmacokinetics of CT-P13 Between Crohn’s Disease and Ulcerative Colitis
Journal of Clinical Gastroenterology, 2022Background: We aimed to compare trough infliximab levels and the development of antidrug antibody (ADA) for 1 year between Crohn’s disease (CD) and ulcerative colitis (UC) patients who were biologic-naive, and to evaluate their impact on clinical outcomes.
Kim, Eun Soo +20 more
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CT-P13 (Inflectra™, Remsima™) monitoring in patients with inflammatory bowel disease
Biologicals, 2016The approval of infliximab biosimilars Remsima™ and Inflectra™ (CT-P13) for patients with inflammatory bowel disease (IBD) is a promising step to reduce treatment costs. Since monitoring of Remicade™ serum trough levels and anti-Remicade™ immunogenicity hold an important significance in treatment modalities, no data about monitoring of drug serum ...
Kornelius, Schulze +5 more
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CT-P13 in the treatment of rheumatoid arthritis
Expert Review of Clinical Immunology, 2017The first biosimilar infliximab, CT-P13 infliximab-dyyb was approved in 2013 by the European Medicines Agency (EMA) and in 2016 by the United States Food and Drug Administration (FDA) and has been used for the treatment of rheumatoid arthritis (RA) for 4 years.
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A Review of CT-P13: An Infliximab Biosimilar
BioDrugs, 2014CT-P13 (Remsima™; Inflectra™), a biosimilar of reference infliximab (Remicade(®)), is approved by the European Medicines Agency for use in all indications for which reference infliximab is approved, including rheumatoid arthritis, ankylosing spondylitis, Crohn's disease, ulcerative colitis, psoriatic arthritis and psoriasis.
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Efficacy of biosimilar infliximab CT-P13 among inpatients with severe steroid-refractory colitis
International Journal of Colorectal Disease, 2020In this study, we evaluate the efficacy and safety of the biosimilar infliximab, CT-P13, in the treatment of inpatients with severe steroid-refractory colitis.A retrospective cohort study of adult colitis patients (UC or isolated Crohn's colitis) admitted to the University of Chicago inflammatory bowel disease inpatient service between January 2018 and
Jacob E. Ollech +8 more
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Subcutaneous Infliximab, CT-P13 SC: A Profile of Its Use in the EU
Clinical Drug Investigation, 2021CT-P13 (Remsima®; Inflectra®), a biosimilar of reference infliximab (Remicade®), provides a useful alternative for patients requiring infliximab therapy and, as with other biosimilar agents, has the potential to reduce treatment costs. Furthermore, the availability of CT-P13 in a subcutaneous formulation (CT-P13 SC), with the possibility (after ...
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Ineffectiveness of infliximab CT‐P13 for the treatment of scleromyxedema: A case report
Dermatologic Therapy, 2017a
Arginelli, Federica +4 more
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A scientific update on biosimilar infliximab (CT-P13) in rheumatic diseases
Expert Review of Clinical Immunology, 2015The development of biologic drugs has undoubtedly enhanced the spectrum of treatments available for immune-mediated inflammatory rheumatic diseases such as rheumatoid arthritis. However, despite their clear clinical benifits, use of biologics is often hindered by their high costs.
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