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Abstracts tagged "Biologicals"

  • Abstract Number: 0903 • ACR Convergence 2020

    Changing Patterns of Use of Biologic/Targeted Synthetic DMARDs in Psoriatic Arthritis: An Analysis of the OPAL Dataset

    Sabina Ciciriello1, Tegan Smith2, Geoffrey Littlejohn3, Kathleen Tymms4, David Mathers5, Helen Cooley6, Hedley Griffiths7, Catherine OSullivan2 and Peter Youssef8, 1Royal Melbourne Hospital, Melbourne, VIC, Melbourne, Victoria, Australia, 2OPAL Rheumatology Ltd, Sydney, NSW, Kogarah, New South Wales, Australia, 3Monash Rheumatology, Clayton, VIC; OPAL Rheumatology Ltd, Sydney, NSW, Melbourne, Victoria, Australia, 4Canberra Rheumatology, Canberra, ACT, Canberra, Australian Capital Territory, Australia, 5Georgetown Rheumatology, Georgetown, NSW, Georgetown, New South Wales, Australia, 6Hobart Private Hospital, Hobart, TAS, Taroona, Australia, 7Barwon Rheumatology Service, Geelong, VIC, Geelong, Victoria, Australia, 8University of Sydney, Sydney, NSW; Royal Prince Alfred Hospital, Camperdown, NSW, Camperdown, New South Wales, Australia

    Background/Purpose: In Australia the cost of biologic/targeted synthetic DMARDs (b/tsDMARDs) for treatment of PsA is subsidized if the patient has documented high levels of clinical/laboratory…
  • Abstract Number: 1226 • ACR Convergence 2020

    Outcomes and Efficacy of Selective versus Automatic Switching from Etanercept to a Biosimilar in Inflammatory Arthritis Using Electronic Health Records from UK

    Roxanne Cooksey1, Sinead Brophy1, Muhammad Azizur1, Jonathan Kennedy1 and Ernest Choy2, 1Swansea University, Swansea, Wales, United Kingdom, 2CREATE Centre, Cardiff University, Cardiff, Wales, United Kingdom

    Background/Purpose: Biosimilars have been approved for the treatment of inflammatory arthritis and evidence from randomised controlled trials have demonstrated equivalent efficacy to biologics.  Etanercept biosimilar,…
  • Abstract Number: 1376 • ACR Convergence 2020

    Impact of Body Composition Measures on the Response to Biological Disease-modifying Anti-rheumatic Drugs in Patients with Ankylosing Spondylitis

    Valeria Rios Rodriguez1, Mikhail Protopopov1, Fabian Proft1, Judith Rademacher1, Burkhard Muche1, Anne-Katrin Weber1, Susanne Lüders1, Hildrun Haibel1, Maryna Verba1, Joachim Sieper1 and Denis Poddubnyy2, 1Charité Universitätsmedizin Berlin, Berlin, Germany, 2Charité – Universitätsmedizin Berlin, Berlin, Germany

    Background/Purpose: Data on the impact of body weight and body mass index (BMI) on the response to biological disease-modifying anti-rheumatic drugs (bDMARDs) in axial spondyloarthritis…
  • Abstract Number: 1764 • ACR Convergence 2020

    Disease Modifying Anti-rheumatic Drug and Biologic Therapy in Pregnancy: A Single-center Mixed Methods Study

    Lauren Glick1, Justin Shamis2, Taneisha McGhie3 and Dharini Mahendira4, 1University of Toronto, Toronto, ON, Canada, 2North York General Hospital, Toronto, ON, Canada, 3Cornwall University Hospital, Kingston, Saint Andrew, Jamaica, 4University of Toronto - Toronto, Toronto, ON, Canada

    Background/Purpose: Rheumatic diseases including rheumatoid arthritis, seronegative inflammatory arthritis and systemic lupus erythematosus can be associated with significant morbidity in women of child-bearing age. Both…
  • Abstract Number: 0003 • ACR Convergence 2020

    Assessing Cytokine Profiles and COVID Serology in Patients on Immunosuppression to Guide Care Recommendations

    Quinn Pritchett1, Rebecca Overbury1, Dorota Lebiedz-Odrobina1, Julie Thomas1, Tawnie Braaten2, Stacey Clardy1, Marc Elgort3, Emily Spivak1, Patricia Slev3, Lisa Peterson3 and Tracy Frech4, 1University of Utah, Salt Lake City, UT, 2University of Utah, Salt Lake City, 3ARUP, Salt Lake City, UT, 4University of Utah and Salt Lake Veterans Affair Medical Center, Salt Lake City, UT

    Background/Purpose: The COVID-19 pandemic is especially terrifying for patients on immunosuppression for autoimmune disease. With the exception of social isolation, experts do not have clear…
  • Abstract Number: 0230 • ACR Convergence 2020

    Effect of Dose Escalation of Subcutaneous Tocilizumab on Disease Activity in Patients with Rheumatoid Arthritis in a Randomized Controlled Trial

    Nora G. Singer1, Shalini V. Mohan2, Jeffrey Yourish3, Jian Han2, Michael Edwardes4 and Margaret Michalska3, 1Case Western Reserve University and MetroHealth System, Cleveland, 2Genentech, South San Francisco, CA, 3Genentech, Inc., South San Francisco, 4Everest Clinical Research, Ontario, Canada

    Background/Purpose: In patients with rheumatoid arthritis (RA), subcutaneous tocilizumab (TCZ-SC) is administered every 2 weeks (q2w) or every week (qw), based on the patient’s weight…
  • Abstract Number: 0356 • ACR Convergence 2020

    Bimekizumab Improves Patient-Reported Outcomes in Psoriatic Arthritis: 48-Week Results from a Phase 2b Study and Association Between Patient-Reported Outcomes and Disease Activity

    Laure Gossec1, Philip Mease2, Alice Gottlieb3, Deepak Assudani4, Jason Coarse5, Barbara Ink6 and Laura Coates7, 1Sorbonne Université and Hôpital Universitaire Pitié Salpêtrière, Paris, France, 2Seattle Rheumatology Associates, P.L.L.C., Seattle, WA, 3Department of Dermatology, Icahn School of Medicine at Mount Sinai, New York, NY, 4UCB Pharma, Slough, United Kingdom, 5UCB Pharma, Raleigh, NC, 6UCB Pharma, Slough, 7University of Oxford, Oxford, United Kingdom

    Background/Purpose: Bimekizumab (BKZ), a humanized monoclonal IgG1 antibody that selectively neutralizes interleukin (IL)-17A and IL-17F, has shown clinical improvements in joint and skin outcomes and…
  • Abstract Number: 0516 • ACR Convergence 2020

    Characteristics of Giant Cell Arteritis Flares After Successful Treatment with Tocilizumab: Results from the Long-Term Extension of a Randomized Controlled Phase 3 Trial

    Sebastian Unizony1, Shalini V. Mohan2, Jian Han2 and John H. Stone1, 1Massachusetts General Hospital Rheumatology Unit, Harvard Medical School, Boston, MA, 2Genentech, South San Francisco, CA

    Background/Purpose: To investigate the characteristics of disease flare after successful treatment with tocilizumab (TCZ) in patients with giant cell arteritis (GCA).Methods: We performed a post…
  • Abstract Number: 0743 • ACR Convergence 2020

    Higher Baseline Fine-Specificity ACPAs Predict Greater Treatment Response with Abatacept + MTX versus MTX Monotherapy in Seropositive RA: A Post Hoc Analysis

    William Robinson1, Chun Wu2, Sarah Hu2, Sean Connolly2 and Sumanta Mukherjee2, 1Stanford University School of Medicine, Stanford, CT, 2Bristol-Myers Squibb Company, Princeton, NJ

    Background/Purpose: ACPAs are sensitive, highly specific markers of RA. Current tests cannot differentiate ACPA+ RA subtypes. Fine-specificity ACPAs (FS) can distinguish between ACPA+ RA subtypes…
  • Abstract Number: 0827 • ACR Convergence 2020

    Comparative Clinical Efficacy of Sarilumab versus Upadacitinib over 12 Weeks: Matching-Adjusted Indirect Comparison Analysis

    Thomas Huizinga1, Ernest Choy2, Amy Praestgaard3, Hubert van Hoogstraten4, Patrick R LaFontaine3, Patricia Guyot5, Daniel Aletaha6, Ulf Müller-Ladner7, Yoshiya Tanaka8, Jeffrey R Curtis9 and Roy Fleischmann10, 1Leiden University Medical Center, Leiden, Netherlands, 2CREATE Centre, Cardiff University, Cardiff, Wales, United Kingdom, 3Sanofi, Cambridge, MA, 4Sanofi, Bridgewater, NJ, 5Sanofi, Chilly-Mazarin, France, 6Division of Rheumatology, Department of Medicine III, Medical University of Vienna,, Vienna, Austria, 7Department of Rheumatology and Clinical Immunology, Justus-Liebig University, Campus Kerckhoff, Bad Nauheim, Germany, 8The First Department of Internal Medicine, University of Occupational and Environmental Health, Kitakyushu, Japan, 9Division of Clinical Immunology and Rheumatology, University of Alabama at Birmingham, Birmingham, AL, 10Southwestern Medical Center, Metroplex Clinical Research Center, Dallas, TX

    Background/Purpose: Sarilumab, an IL-6 receptor inhibitor, and upadacitinib, a Janus kinase (JAK) 1 inhibitor, are both approved for the treatment of patients with moderately to…
  • Abstract Number: 0906 • ACR Convergence 2020

    Bimekizumab Treatment Is Associated with Improvements in Back Pain and Fatigue in Patients with Active Psoriatic Arthritis: 48-Week Results from a Phase 2b Study

    Atul Deodhar1, Laure Gossec2, Philip Mease3, Jason Coarse4, Heather Edens5, Natasha de Peyrecave6, Deepak Assudani6, Barbara Ink7 and Christopher Ritchlin8, 1Oregon Health & Science University, Portland, OR, 2Sorbonne Université and Hôpital Universitaire Pitié Salpêtrière, Paris, France, 3Seattle Rheumatology Associates, P.L.L.C., Seattle, WA, 4UCB Pharma, Raleigh, NC, 5UCB Pharma, Smyrna, GA, 6UCB Pharma, Slough, United Kingdom, 7UCB Pharma, Slough, 8Department of Medicine, University of Rochester Medical Center, Rochester, NY

    Background/Purpose: Patients (pts) with psoriatic arthritis (PsA) require effective treatment across all symptoms. Bimekizumab (BKZ) is a humanized IgG1 monoclonal antibody which selectively neutralizes interleukin…
  • Abstract Number: 1236 • ACR Convergence 2020

    Association Between Change in Health Assessment Questionnaire Disability Index and Treatment Response in Patients with Rheumatoid Arthritis in Tocilizumab Clinical Trials

    Sebastian Unizony1, Joseph Dang2, Jian Han3, Margaret Michalska2 and Jennie H. Best2, 1Massachusetts General Hospital Rheumatology Unit, Harvard Medical School, Boston, MA, 2Genentech, Inc., South San Francisco, 3Genentech, South San Francisco, CA

    Background/Purpose: The efficacy and safety of intravenous (IV) and subcutaneous (SC) tocilizumab (TCZ) in combination with conventional synthetic disease-modifying antirheumatic drugs (csDMARDs) and as monotherapy…
  • Abstract Number: 1427 • ACR Convergence 2020

    Anti-IL5 Therapy for Eosinophilic Granulomatosis with Polyangiitis (EGPA) – An 18 Month Follow-up Study as a Steroid Sparing Therapeutic Approach

    Allyson Egan1, Pasupathy Sivasothy2, Robin Gore3, Caroline Owen3, Marcos Del Martinez Pero4, Rachel Jones4, Lisa Willcocks4, Rona Smith4, Stella Burns4 and David Jayne5, 1Vasculitis and Lupus Clinic, Department of Medicine, Addenbrooke's Hospital, Cambridge., London, United Kingdom, 2Vasculitis and Lupus Clinic, Department of Medicine, Addenbrooke's Hospital, Cambridge., Cambridge, England, United Kingdom, 3Department of Respiratory medicine, Addenbrooke's Hospital, Cambridge, Cambridge, United Kingdom, 4Vasculitis and Lupus Clinic, Department of Medicine, Addenbrooke's Hospital, Cambridge., Cambridge, 5Department of Medicine, Vasculitis and Lupus Research Group, University of Cambridge, Cambridge, UK, Cambridge, United Kingdom

    Background/Purpose: EGPA is a small vessel vasculitis characterized by the presence of tissue eosinophilia, necrotizing vasculitis and granulomatous inflammation1. In the randomized, placebo-controlled MIRRA trial…
  • Abstract Number: 1826 • ACR Convergence 2020

    ­Maintenance of Efficacy and Safety and Reduction of BILAG Flares with Ustekinumab, an Interleukin-12/23 Inhibitor, in Patients with Active Systemic Lupus Erythematosus: 2-Year Results of a Phase 2, Randomized Placebo-Controlled, Crossover Study

    Ronald van Vollenhoven1, Bevra Hahn2, George Tsokos3, Peter Lipsky4, Robert Gordon5, Kaiyin Fei6, Kim Hung Lo7, Marc Chevrier8, Qing Zuraw9, Pamela Berry10, Chetan Karyekar10 and Shawn Rose11, 1Department of Rheumatology, Amsterdam Rheumatology and Immunology Center, Amsterdam, Netherlands, 2University of California Los Angeles, Encino, CA, 3Division of Rheumatology & Clinical Immunology/Beth Israel Deaconess Medical Center/Harvard Medical School, Boston, MA, 4RILITE Foundation, Charlottesville, VA, 5Janssen Research & Development, LLC, Chester Springs, PA, 6Janssen Research & Development, LLC, Spring House, PA, 7Janssen Research & Development, LLC, Spring House, 8Janssen Research & Development, LLC, Collegeville, PA, 9Janssen Research & Development, LLC, Wayne, PA, 10Janssen Global Services, LLC, Horsham, PA, 11Janssen Research & Development, LLC, Princeton Junction, NJ

    Background/Purpose: Both IL-12 and IL-23 have been implicated in the pathogenesis of SLE. In a phase 2 study, treatment with the anti-IL-12/23 p40 monoclonal antibody…
  • Abstract Number: 0008 • ACR Convergence 2020

    COVID-19 Infection Among Patients with Rheumatic Disease on Biologic & Targeted Therapies: A Systematic Review

    Akhil Sood1, Arbi Galestanian1, Vijaya Murthy2, Emilio Gonzalez1 and Mukaila Raji1, 1University of Texas Medical Branch, Galveston, TX, 2University of Texas Medical Branch, League City, TX

    Background/Purpose: Information about the outcomes of patients with rheumatic disease with SARS-CoV-2 infection is scarce. Patients with rheumatic disease on immunosuppressive medications might represent a…
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Embargo Policy

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 CT on October 25. 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.).

Violation of this policy may result in the abstract being withdrawn from the meeting and other measures deemed appropriate. Authors are responsible for notifying colleagues, institutions, communications firms, and all other stakeholders related to the development or promotion of the abstract about this policy. If you have questions about the ACR abstract embargo policy, please contact ACR abstracts staff at [email protected].

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