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Background: CT-P13 is a biosimilar of Remicade©, an agent approved in some countries for use in inflammatory bowel disease (IBD). Controlled clinical trials have demonstrated the efficacy and safety of CT-P13 in rheumatic diseases, but not in IBD.
Angel Vilches-Arenas +1 more
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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
openaire +2 more sources
BACKGROUND: The infliximab biosimilar CT-P13 was approved for use in Crohn's disease after clinical comparison with originator infliximab in ankylosing spondylitis and rheumatoid arthritis; however, concerns about such indication extrapolation have been ...
HoUng Kim, Chang Soo Eun, Byong Duk Ye
exaly +2 more sources
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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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 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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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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CT-P13: a review on a biosimilar to infliximab in the treatment of inflammatory bowel disease
Expert Opinion on Biological Therapy, 2019Introduction: CT-P13 was developed as an infliximab biosimilar in 2013. The primary structure of CT-P13 is identical to that of original infliximab and it has highly similar higher order structure, physiochemical characteristics, and biological properties.
Ahmad Albshesh, Shomron Ben-Horin
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Clinical and Experimental Rheumatology, 2021
Paediatric non-infectious uveitis (NIU) is an important cause of significant long-term complications and blindness in children. Infliximab (IFX) is a chimeric human/murine monoclonal antibody against TNF-α that is effective in NIU resistant to conventional therapies.
Betül, Sözeri +4 more
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Paediatric non-infectious uveitis (NIU) is an important cause of significant long-term complications and blindness in children. Infliximab (IFX) is a chimeric human/murine monoclonal antibody against TNF-α that is effective in NIU resistant to conventional therapies.
Betül, Sözeri +4 more
openaire +2 more sources

