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Anti-TNF biosimilars for rheumatic diseases: the key to early treatment?

Anti-TNF biosimilars webinar

Read time: 55 mins
Last updated:5th May 2022
Published:5th May 2022

Would you like to learn more about how anti-TNF biosimilars fit into management of rheumatoid arthritis? Join Professor Peter C Taylor in our webinar series to discover:

  • Key clinical evidence for safety and efficacy of anti-TNF biosimilars in rheumatoid arthritis
  • Expert discussion on how anti-TNF biosimilars can address unmet needs in rheumatoid arthritis, including early treatment access
  • Tips for switching to biosimilars in practice

Anti-TNF biosimilars in rheumatoid arthritis - evidence for place in therapy

Chaired by Professor Peter C. Taylor from Oxford University (UK) and joined by guest faculty Professor Christopher Edwards from University Hospital Southampton NHS Foundation Trust (UK) this webinar explores the clinical evidence behind anti-TNF biosimilars in rheumatoid arthritis (RA), how anti-TNF biosimilars can help to address unmet needs, and how they fit into management.

Watch the webinar

Watch the full 30-minute webinar on ‘Anti-TNF biosimilars in rheumatoid arthritis – evidence for place in therapy’ which took place 28 April 2022 to hear in-depth discussion about the clinical evidence, potential for early treatment and the audience Q&A on how biosimilars fit into the RA treatment landscape.

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Meet the experts

Professor Peter Taylor.pngProfessor Peter C. Taylor

Professor Taylor is the Director of Clinical Sciences, Botnar Research Centre, University of Oxford, United Kingdom. He 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 trials of anti-TNF and anti-IL-6 receptor therapy. Professor Taylor has specialist clinical interests in novel therapies, rheumatoid and early arthritis.

Disclosures: Professor Taylor has declared research grants from Celgene and Galapagos, and consultation fees from AbbVie, Biogen, Fresenius, Galapagos, Gilead, GlaxoSmithKline, Janssen, Eli Lilly, Nordic Pharma, Novartis, Pfizer, Roche, Sanofi and UCB.

 

Professor Christopher Edwards.jpgProfessor Christopher Edwards

Professor Edwards is Co-Director of the NIHR Southampton Clinical Research Facility, University Hospital Southampton NHS Foundation Trust, United Kingdom. He is Clinical Director of the Southampton Musculoskeletal Research Unit, a recognised EULAR centre of excellence, and is the Chair of the EULAR Education Committee. As Co-Director of the NIHR Southampton Clinical Research Facility, he is engaged with running a large translational research facility with first-in-human and phase 1 experience. 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).  

Disclosures: Professor Edwards has declared receiving fees from AbbVie, Biogen, Bristol Myers Squibb, Celgene, Eli Lilly, Fresenius, Galapagos, Gilead, GlaxoSmithKline, Janssen, Novartis, Pfizer, Roche, Sanofi, for the following activities: advisory boards, speaker’s bureau, and research support.

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