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Abstracts tagged "certolizumab pegol and rheumatoid arthritis"

  • Abstract Number: 1846 • 2012 ACR/ARHP Annual Meeting

    Observation of Persistence Rates and Potential Costs Savings Associated with Certolizumab Pegol Treatment for Rheumatoid Arthritis in England, Wales and Northen Ireland Clinical Practice

    Mike Russell1, Jen Timoshanko1, Graeme Duncan2, Angela Spandley1 and Samantha Roskell3, 1UCB Pharma, Slough, United Kingdom, 2Healthcare at Home Ltd, Burton on Trent, United Kingdom, 3Rheumatology, Cannock Chase Hospital, Cannock, United Kingdom

    Background/Purpose: Rheumatoid arthritis (RA) therapy in the UK is standardized by the National Institute for Health and Clinical Excellence (NICE).  To be eligible for anti-TNF…
  • Abstract Number: 1316 • 2012 ACR/ARHP Annual Meeting

    Long-Term Safety and Efficacy of 4-Weekly Certolizumab Pegol Combination and Monotherapy in Rheumatoid Arthritis: 5 Year Results from an Open Label Extension Study

    Roy Fleischmann1, Ronald F. van Vollenhoven2, Jiri Vencovsky3, Rieke Alten4, Owen Davies5, Christian Stach6, Marc de Longueville7, Brenda Van Lunen8 and Ernest Choy9, 1University of Texas Southwestern Medical Center at Dallas, Dallas, TX, 2Karolinska Institute, Stockholm, Sweden, 3Institute of Rheumatology, Prague, Czech Republic, 4Teaching Hospital of the Charité, University of Berlin, Berlin, Germany, 5UCB Pharma, Slough, United Kingdom, 6UCB Pharma, Monheim, Germany, 7Global Medical Affairs, UCB Pharma, Brussels, Belgium, 8UCB Pharma, Raleigh, NC, 9Section of Rheumatology, Cardiff University School of Medicine, Cardiff, United Kingdom

    Background/Purpose: Certolizumab pegol (CZP) has been shown to be efficacious and have an acceptable safety profile when administered every 4 weeks (Q4W) as monotherapy (FAST4WARD,…
  • Abstract Number: 1318 • 2012 ACR/ARHP Annual Meeting

    Long-Term Benefits of 4-Weekly Certolizumab Pegol Combination and Monotherapy On Household Productivity and Social Participation in Rheumatoid Arthritis: 5 Year Results from an Open Label Extension Study

    Vibeke Strand1, Oana Purcaru2, Ronald F. van Vollenhoven3, Ernest Choy4 and Roy Fleischmann5, 1Adjunct, Division of Immunology / Rheumatology, Stanford University, Portola Valley, CA, 2UCB Pharma, Brussels, Belgium, 3Karolinska Institute, Stockholm, Sweden, 4Section of Rheumatology, Cardiff University School of Medicine, Cardiff, United Kingdom, 5Southwestern Medical Center at Dallas, University of Texas, Dallas, TX

    Background/Purpose: Certolizumab pegol (CZP) monotherapy administered every 4 weeks (Q4W) for rheumatoid arthritis (RA) has been shown to be associated with rapid and sustainable improvements…
  • Abstract Number: 1319 • 2012 ACR/ARHP Annual Meeting

    Certolizumab Pegol Plus Methotrexate Is Similarly Effective in Active Rheumatoid Arthritis  Secondary Non-Responders to Anti-TNF Inhibitors: Post-Hoc Analysis of a Phase Iiib Trial

    Daniel Furst1, Saeed A. Shaikh2, Maria W. Greenwald3, Michael H. Schiff4, Barbara Bennett5, Owen Davies6, Fabienne Staelens7, Will Koetse8 and Philippe Bertin9, 1David Geffen School of Medicine, Div of Rheumatology, University of California at Los Angeles, Los Angeles, CA, 2Medicine, McMaster University, St Catharines, ON, Canada, 3Desert Medical Advances, Palm Desert, CA, 4Rheumatology Division, University of Colorado, Denver, CO, 5BABennett Consulting, LLC, Marietta, GA, 6UCB Pharma, Slough, United Kingdom, 7UCB Pharma, Brussels, Belgium, 8UCB Pharma, Rtp, NC, 9Service De Rhumatologie, Dupuytren Hospital, Limoges, France

    Background/Purpose: Certolizumab pegol (CZP) has demonstrated efficacy in patients (pts) with prior TNF inhibitor exposure.1 In the Doseflex trial two maintenance dosing regimens of CZP…
  • Abstract Number: 1312 • 2012 ACR/ARHP Annual Meeting

    Clinical Response At 12 Weeks Predicts Long-Term Remission and the Extent of Radiographic Progression in Japanese Patients with Rheumatoid Arthritis Treated with Certolizumab Pegol with and without Methotrexate Coadministration

    Tsutomu Takeuchi1, Kazuhiko Yamamoto2, Hisashi Yamanaka3, Naoki Ishiguro4, Yoshiya Tanaka5, Katsumi Eguchi6, Akira Watanabe7, Hideki Origasa8, Toshiharu Shoji9, Nobuyuki Miyasaka10 and Takao Koike11, 1Keio University School of Medicine, Tokyo, Japan, 2Department of Allergy & Rheumatology, Graduate School of Medicine, The University of Tokyo, Bunkyo-ku, Tokyo, Japan, 3Institute of Rheumatology, Tokyo Women's Medical University, Tokyo, Japan, 4Department of Orthopedic Surgery, Nagoya University, Graduate School & Faculty of Medicine, Nagoya, Aichi, Japan, 5The First Department of Internal Medicine, University of Occupational and Environmental Health, Japan, Kitakyushu, Japan, 6Sasebo City General Hospital, Sasebo, Nagasaki, Japan, 7Research Division for Development of Anti-Infectious Agents, Institute of Development, Aging and Cancer, Tohoku University, Sendai, Miyagi, Japan, 8Division of Biostatistics and Clinical Epidemiology, University of Toyama School of Medicine, Toyama, Toyama, Japan, 9Department of Clinical Research and Development, Otsuka Pharmaceutical Co., Ltd, Shinagawa-ku, Tokyo, Japan, 10Department of Medicine and Rheumatology and Global Center of Excellence Program, Tokyo Medical and Dental University, Tokyo, Japan, 11Sapporo medical center NTT EC, Sapporo, Japan

    Background/Purpose: The majority of patients (pts) with active rheumatoid arthritis (RA) have previously been shown to respond during the first 12 weeks (wks)  of certolizumab…
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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.

Accepted abstracts are made available to the public online in advance of the meeting and are published in a special online supplement of our scientific journal, Arthritis & Rheumatology. Information contained in those abstracts may not be released until the abstracts appear online. In an exception to the media embargo, academic institutions, private organizations, and companies with products whose value may be influenced by information contained in an abstract may issue a press release to coincide with the availability of an ACR abstract on the ACR website. However, the ACR continues to require that information that goes beyond that contained in the abstract (e.g., discussion of the abstract done as part of editorial news coverage) is under media embargo until 10:00 AM ET on November 14, 2024. Journalists with access to embargoed information cannot release articles or editorial news coverage before this time. Editorial news coverage is considered original articles/videos developed by employed journalists to report facts, commentary, and subject matter expert quotes in a narrative form using a variety of sources (e.g., research, announcements, press releases, events, etc.).

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