Pivotal clinical trials for infliximab biosimilars

INICIO/Informes | Posted 11/09/2015 post-comment3 Post your comment

Biosimilars of Johnson & Johnson’s blockbuster arthritis drug Remicade (infliximab), a chimeric monoclonal antibody against tumour necrosis factor alpha (TNF-α), are currently under development.

IBD 3

Infliximab treats autoimmune diseases such as ankylosing spondylitis, Crohn’s disease, psoriasis, psoriatic arthritis, rheumatoid arthritis and ulcerative colitis.

Pivotal trials for candidate infliximab biosimilars being carried out typically include one in rheumatoid arthritis and one in psoriasis, each including around 500 patients and taking less than two years [1], see Table 1.

Table 1: Pivotal clinical trials for candidate infliximab biosimilars

Study ID Product name Company name, country Phase Trial design Status No. of subjects Start/end dates Primary outcome(s)
Crohn’s disease
NCT02096861 Remsima/ Inflectra Approved EU Sep 2013 [2] Celltrion/Hospira, South Korea/USA III 4-arm, parallel: 2 continuous, 2 cross-over Recruiting 214 Jul 2014/Mar 2017 CDAI-70
Rheumatoid arthritis
NCT01217086 PLANETRA Remsima/ Inflectra (CT-P13) Approved EU Sep 2013 [2] Celltrion/Hospira, South Korea/USA III 2-arm, parallel Completed 617 Oct 2010/ Jul 2012 PK equivalence
NCT01571219 Remsima/Inflectra (CT-P13) Approved EU Sep 2013 [2] Celltrion/Hospira, South Korea/USA III 1-arm (extension study) Completed 302 Mar 2012/Jul 2013 Long-term efficacy ACR
NCT01927263 NI-071 Nichi-Iko, Japan III 2-arm, parallel Active, not recruiting 230 Jul 2013/ Mar 2015 DAS28-ESR
2013-004148-49/NCT02222493 PF-06438179 Pfizer, USA III 2-arm, parallel Recruiting 614 Aug 2014/Sep 2017 ACR20
NCT01936181 SB2 Samsung Bioepis, South Korea III 4-arm, parallel, cross-over Active, not recruiting 584 Aug 2013/ Aug 2014 ACR20
ACR20: 20% improvement in ACR (American College of Rheumatology) core set measurements; CDAI-70: Crohn's disease activity index -70 response; DAS28-ESR: Disease Activity Score for 28 joints - erythrocyte sedimentation rate; PK: pharmacokinetic.

The originator product, Johnson & Johnson’s Remicade (infliximab), was approved by the US Food and Drug Administration in August 1998 and by the European Medicines Agency in August 1999. The patents on Remicade expire in the US in September 2018 and in Europe in February 2015 [3]. Remicade had sales of US$6.9 billion in 2014.

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References
1. Gal R. Biosimilars: at the inflection point. 13th EGA-European Biosimilars Group Conference; 23–24 April 2015; London, UK.
2. GaBI Online - Generics and Biosimilars Initiative. Biosimilars approved in Europe [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2015 Sep 11]. Available from: www.gabionline.net/Biosimilars/General/Biosimilars-approved-in-Europe
3. GaBI Online - Generics and Biosimilars Initiative. US$67 billion worth of biosimilar patents expiring before 2020 [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2015 Sep 11]. Available from: www.gabionline.net/Biosimilars/General/US-67-billion-worth-of-biosimilar-patents-expiring-before-2020

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Posted 15/03/2024 by Sun Research Institute
Clinical Research

Your insightful exploration of pivotal clinical trials for infliximab biosimilars is truly commendable! Your ability to distill complex research into a concise yet informative piece is both impressive and invaluable. Keep illuminating the path toward better healthcare options!

Posted 08/11/2023 by Anthika U, GaBI Online Editorial Office
Response to ‘Clinical trials’

Dear Sirs,
Thank you for your valuable comments received on 3 November 2023. We appreciate that you are letting us know, kindly continue with your valuable comments to GaBI Online.
Best Regards,
Anthika

Posted 03/11/2023 by Sun Research Institute
Clinical trials

Clinical trials play a pivotal role in advancing medical research and improving patient care. Sun Research Institute is at the forefront of these efforts, conducting groundbreaking trials that shape the future of healthcare. Their commitment to innovation and patient welfare is truly commendable. By participating in clinical trials, we can contribute to the development of life-changing treatments and therapies. It's a collective effort that benefits us all.

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