Anti-tumour necrosis factor (TNF) biosimilars have emerged as a cost-effective treatment option in rheumatic diseases, with potential to improve global inequities in treatment access. Explore:
- Unmet needs in rheumatic disease management, and how anti-TNF biosimilars can facilitate early treatment access
- Benefits of early treatment with anti-TNFs in rheumatic diseases, compared to delayed initiation
- Our Webinar series with expert commentary on anti-TNF biosimilars versus their reference biologics, and tips for integration into clinical practice
This Learning Zone explores unmet needs in rheumatic disease management, including inequities in treatment access, and how anti-TNF biosimilars can help to address this gap. Discover more about TNF as a treatment target, the range of anti-TNF biosimilars available, biosimilar development and the clinical benefits of early initiation of anti-TNFs compared to delayed initiation.
Our webinar series, chaired by Professor Peter Taylor, explores the evidence for anti-TNF biosimilars in rheumatoid arthritis and spondyloarthritis, providing expert insights into integration of biosimilars in clinical practice.
Missed Webinar 1?
Meet the experts
Professor Peter Taylor
Professor Peter C. Taylor trained at Cambridge and Oxford Universities and gained a PhD from the University of London. He holds the Norman Collisson chair of musculoskeletal sciences at Oxford University where he is the Director of Clinical Sciences at the Botnar Research Centre. Professor Taylor has over thirty years of experience in clinical trial design and international leadership in studies of biologic and small molecular therapies in rheumatoid arthritis, psoriatic arthritis and ankylosing spondylitis including the earliest seminal trails of anti-TNF and anti-IL-6 receptor therapy. He has specialist clinical interests in novel therapies, rheumatoid and early arthritis.
Financial disclosures: Professor Taylor has declared research grants from Celgene, Galapagos; and consultation fees from AbbVie, Biogen, Galapagos, Gilead, GlaxoSmithKline, Janssen, Novartis, Lilly, Pfizer, Roche, Sanofi, Nordic Pharma, Fresenius and UCB.
Professor Christopher Edwards
Professor Edwards is a Consultant Rheumatologist and Co-Director of the NIHR Southampton Clinical Research Facility within the University Hospital Southampton NHS Foundation Trust, having previously worked as a consultant at Tan Tock Seng Hospital in Singapore. Professor Edwards trained with Professor Maini at the Kennedy Institute of Rheumatology during the early years of anti-TNF trials and with Professor Graham Hughes at the St Thomas’ Hospital Lupus Clinic in London. He has been an Investigator on a number of clinical trials of therapies for inflammatory rheumatic diseases and more recently has worked on COVID vaccine (Oxford/Astra-Zeneca studies and COVBOOST) and therapeutic studies (AGILE Platform). As Co-Director of the NIHR Southampton Clinical Research Facility he is engaged with the running of a large translational research facility with FIH and phase I experience. Professor Edwards is Clinical Director of the Southampton Musculoskeletal Research Unit, a recognised EULAR centre of excellence and is the Chair of the EULAR Education Committee.
Financial disclosures: Professor Edwards has declared honoraria, advisory boards, speakers bureau, research support from Abbvie, BMS, Biogen, Celgene, Fresenius, Gilead, Janssen, Lilly, Mundipharma, Pfizer, MSD, Novartis, Roche, Samsung, Sanofi and UCB.
Developed by EPG Health for Medthority. This content has been developed independently of the sponsor, Sandoz, who has had no editorial input into the content. Medthority received unrestricted educational grant funding from the sponsor in order to help provide its healthcare professional members with access to the highest quality medical and scientific information and associated relevant content, without any promotional intent. This content is intended for healthcare professionals only.