CT-P13: design, development, and place in therapy

Tommaso Gabbani,1 Simona Deiana,2 Vito Annese3 1Gastroenterology Unit, Morgagni-Pierantoni Hospital, AUSL Romagna, Forlì, 2Division of Gastroenterology, AOU Careggi University Hospital, Florence, Italy; 3Gastroenterology Department, Valiant Clinic, Dubai, UAE Abstract: The introduction...

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Main Authors: Gabbani T, Deiana S, Annese V
Format: Article
Language:English
Published: Dove Medical Press 2017-06-01
Series:Drug Design, Development and Therapy
Subjects:
Online Access:https://www.dovepress.com/ct-p13-design-development-and-place-in-therapy-peer-reviewed-article-DDDT
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spelling doaj-4816719ab5ca4922a6f34679f7a1dcf12020-11-24T22:54:39ZengDove Medical PressDrug Design, Development and Therapy1177-88812017-06-01Volume 111653166133154CT-P13: design, development, and place in therapyGabbani TDeiana SAnnese VTommaso Gabbani,1 Simona Deiana,2 Vito Annese3 1Gastroenterology Unit, Morgagni-Pierantoni Hospital, AUSL Romagna, Forlì, 2Division of Gastroenterology, AOU Careggi University Hospital, Florence, Italy; 3Gastroenterology Department, Valiant Clinic, Dubai, UAE Abstract: The introduction of biological agents has revolutionized the management of many life-threatening and debilitating immune-mediated diseases. Because of the high cost of biological drugs and their patent expiration, the market has opened to biosimilar agents, copy versions of the originators, which can lead to reduced health care expenditure and increase treatment access worldwide. CT-P13 is the first biosimilar of infliximab (IFX) and has been approved for the same indications as its originator drug. It obtained regulatory approval by the European Medicines Agency in September 2013 and by the US Food and Drug Administration in April 2016. The Phase I and Phase III clinical trials conducted in ankylosing spondylitis and rheumatoid arthritis have demonstrated pharmacokinetic and efficacy equivalence with comparable safety and immunogenicity to IFX. For these reasons, the use of CT-P13 has been extrapolated also to inflammatory bowel disease. There have been some initial concerns regarding the use of CT-P13 in inflammatory bowel disease patients, because of the lack of randomized controlled trials. However, emerging real-world data have further confirmed the comparability between CT-P13 and its reference product in terms of efficacy, safety, and immunogenicity, in patients naïve to the anti-tumor necrosis factor alpha agents and after switching from IFX, and will be summarized in this review. Keywords: CT-P13, infliximab, biosimilar, biologic therapy, Crohn’s disease, ulcerative colitishttps://www.dovepress.com/ct-p13-design-development-and-place-in-therapy-peer-reviewed-article-DDDTCT-P13Infliximabbiosimilarbiologic therapyCrohn diseaseUlcerative Colitis
collection DOAJ
language English
format Article
sources DOAJ
author Gabbani T
Deiana S
Annese V
spellingShingle Gabbani T
Deiana S
Annese V
CT-P13: design, development, and place in therapy
Drug Design, Development and Therapy
CT-P13
Infliximab
biosimilar
biologic therapy
Crohn disease
Ulcerative Colitis
author_facet Gabbani T
Deiana S
Annese V
author_sort Gabbani T
title CT-P13: design, development, and place in therapy
title_short CT-P13: design, development, and place in therapy
title_full CT-P13: design, development, and place in therapy
title_fullStr CT-P13: design, development, and place in therapy
title_full_unstemmed CT-P13: design, development, and place in therapy
title_sort ct-p13: design, development, and place in therapy
publisher Dove Medical Press
series Drug Design, Development and Therapy
issn 1177-8881
publishDate 2017-06-01
description Tommaso Gabbani,1 Simona Deiana,2 Vito Annese3 1Gastroenterology Unit, Morgagni-Pierantoni Hospital, AUSL Romagna, Forlì, 2Division of Gastroenterology, AOU Careggi University Hospital, Florence, Italy; 3Gastroenterology Department, Valiant Clinic, Dubai, UAE Abstract: The introduction of biological agents has revolutionized the management of many life-threatening and debilitating immune-mediated diseases. Because of the high cost of biological drugs and their patent expiration, the market has opened to biosimilar agents, copy versions of the originators, which can lead to reduced health care expenditure and increase treatment access worldwide. CT-P13 is the first biosimilar of infliximab (IFX) and has been approved for the same indications as its originator drug. It obtained regulatory approval by the European Medicines Agency in September 2013 and by the US Food and Drug Administration in April 2016. The Phase I and Phase III clinical trials conducted in ankylosing spondylitis and rheumatoid arthritis have demonstrated pharmacokinetic and efficacy equivalence with comparable safety and immunogenicity to IFX. For these reasons, the use of CT-P13 has been extrapolated also to inflammatory bowel disease. There have been some initial concerns regarding the use of CT-P13 in inflammatory bowel disease patients, because of the lack of randomized controlled trials. However, emerging real-world data have further confirmed the comparability between CT-P13 and its reference product in terms of efficacy, safety, and immunogenicity, in patients naïve to the anti-tumor necrosis factor alpha agents and after switching from IFX, and will be summarized in this review. Keywords: CT-P13, infliximab, biosimilar, biologic therapy, Crohn’s disease, ulcerative colitis
topic CT-P13
Infliximab
biosimilar
biologic therapy
Crohn disease
Ulcerative Colitis
url https://www.dovepress.com/ct-p13-design-development-and-place-in-therapy-peer-reviewed-article-DDDT
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