ACR Meeting Abstracts

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Abstracts tagged "Biosimilars and etanercept"

  • Abstract Number: 2511 • 2018 ACR/ARHP Annual Meeting

    Benepali Switches in Clinical Practice – a Positive Single Centre Experience

    Hoda Alkoky, Angela Pakozdi and Hasan Tahir, Rheumatology, Barts Health NHS Trust, London, United Kingdom

    Background/Purpose: Benepali (SB4) an etanercept (ETN) biosimilar, has demonstrated comparable efficacy in randomised controlled trials. Switching patients to biosimilars has cost benefits to the national…
  • Abstract Number: 2533 • 2018 ACR/ARHP Annual Meeting

    Switching Patients with Arthritis from Etanercept (Enbrel) to the Biosimilar Drug, Benepali: A Single- Center Retrospective Observational Study

    Anastasia- Vasiliki Madenidou1, Andrew Jeffries2, Sneha Varughese2, Stephen Jones2, Helen Veevers2, Hanadi Sari- Kouzel2 and Chandini Rao2, 1Rheumatology, Blackpool Teaching Hospitals NHS Foundation Trust, Blackpool, United Kingdom, 2Blackpool Teaching Hospitals NHS Foundation Trust, Blackpool, United Kingdom

    Background/Purpose: Benepali, the etanercept biosimilar, is licenced in the UK for the same indications as the reference product, Enbrel.In 2016, the Rheumatology Department at Blackpool…
  • Abstract Number: 2550 • 2018 ACR/ARHP Annual Meeting

    Phase 3 Equira 48 Week Study Results Demonstrated No Impact on Efficacy and Safety When Patients with Moderate-to-Severe Rheumatoid Arthritis Were Switched between Reference Etanercept (ETN) and GP2015, an Etanercept Biosimilar

    Arthur Kavanaugh1, Marco Matucci-Cerinic2, Hendrik Schulze-Koops3, Maya Buch4, Yannick Allanore5, Eugeniusz J. Kucharz6 and Goran Babic7, 1UC San Diego School of Medicine, La Jolla, California, La Jolla, CA, 2Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy, 3Ludwig-Maximilians-University, Munich, Germany, Munich, Germany, 4University of Leeds, United Kingdom, Leeds, United Kingdom, 5Cochin Hospital, Paris Descartes University, Paris, France, Paris, France, 6Department of Internal Medicine and Rheumatology, Medical University of Silesia, Katowice, Poland, Katowice, Poland, 7Hexal AG, a Sandoz company, Holzkirchen, Germany, Holzkirchen, Germany

    Background/Purpose: Compared to ETN, GP2015 has equivalent efficacy, and comparable safety and immunogenicity in patients with chronic plaque-type psoriasis.1 The purpose of this study is…
  • Abstract Number: 1470 • 2017 ACR/ARHP Annual Meeting

    Impact of Anti-Drug Antibody and Injection Site Reaction on Efficacy: 24-Week Results from a Phase III Study Comparing SB4 (etanercept biosimilar) with Reference Etanercept in Patients with Rheumatoid Arthritis

    Jiri Vencovsky1, Paul Emery2, Edward C. Keystone3, Jeehoon Ghil4, Soo Yeon Cheong4 and Evelyn Hong4, 1Institute of Rheumatology, Deartment of Rheumatology, 1st Faculty of Medicine, Charles University, Prague, Czech Republic, 2NIHR-Leeds Musculoskeletal Biomedical Research Unit and Leeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds, Leeds, United Kingdom, 3University of Toronto, Toronto, ON, Canada, 4Samsung Bioepis Co., Ltd., Incheon, Korea, Republic of (South)

    Background/Purpose : SB4 is approved by the European Commission as a biosimilar of the reference etanercept (ETN). The phase III clinical study results have been…
  • Abstract Number: 2467 • 2017 ACR/ARHP Annual Meeting

    Evaluation of Radiographic Progression By Disease Activity States in Patients with Rheumatoid Arthritis Treated with SB4 or Reference Etanercept: Results from a Phase III Study

    Paul Emery1, Jiri Vencovsky2, Jeehoon Ghil3, Soo Yeon Cheong3 and Evelyn Hong3, 1NIHR-Leeds Musculoskeletal Biomedical Research Unit and Leeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds, Leeds, United Kingdom, 2Institute of Rheumatology, Deartment of Rheumatology, 1st Faculty of Medicine, Charles University, Prague, Czech Republic, 3Samsung Bioepis Co., Ltd., Incheon, Korea, Republic of (South)

    Background/Purpose : SB4 has been approved as a biosimilar of the reference etanercept by the European Commission. Results including one year radiographic progression from the…
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All abstracts accepted to ACR Convergence are under media embargo once the ACR has notified presenters of their abstract’s acceptance. They may be presented at other meetings or published as manuscripts after this time but should not be discussed in non-scholarly venues or outlets. The following embargo policies are strictly enforced by the ACR.

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