ACR Meeting Abstracts

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Abstracts tagged "Adalimumab"

  • Abstract Number: 1641 • 2012 ACR/ARHP Annual Meeting

    When Can Biological Therapy Be Resumed in Patients with Rheumatic Conditions Who Develop Tuberculosis Infection During Tumour Necrosis Factors Antagonists Therapy? Study Based On the Biobadaser Data Registry

    Maria Victoria Hernández1, Miguel A. Descalzo2, Juan D. Cañete1, Raimon Sanmarti3 and BIOBADASER Study Group4, 1Rheumatology, Hospital Clínic of Barcelona. IDIBAPS. University of Barcelona, Barcelona, Spain, 2Research Unit, Spanish Society of Rheumatology, Madrid, Spain, 3Arthritis Unit. Rheumatology Department, Hospital Clínic of Barcelona, Barcelona, Spain, 4Research Unit. Spanish Society of Rheumatology, Madrid, Spain

    Background/Purpose: Tuberculosis infection (TI) is one of the most serious adverse events related to tumour necrosis factor (TNF) antagonists. According to the current treatment guidelines…
  • Abstract Number: 487 • 2012 ACR/ARHP Annual Meeting

    Functional Disability in Early Rheumatoid Arthritis – Contributions of Disease Activity and Structural Damage, and the Impact of Different Treatment Strategies

    Josef S. Smolen1, Roy Fleischmann2, Paul Emery3, Ronald F. van Vollenhoven4, Stefan Florentinus5, Freddy Faccin6, Suchitrita S. Rathmann7, Hartmut Kupper8 and Arthur Kavanaugh9, 1Medical University of Vienna and Hietzing Hospital, Vienna, Austria, 2Southwestern Medical Center at Dallas, University of Texas, Dallas, TX, 3Medicine, Leeds Musculoskeletal Biomedical Research Unit, Leeds, United Kingdom, 4Unit for Clinical Trial Therapy research, The Karolinska Institute, Stockholm, Sweden, 5AbbVie, Rungis, France, 6Abbott, Abbott Park, IL, 7Abbott Laboratories, Abbott Park, IL, 8Immunology Development, Abbott GmbH and Co. KG, Ludwigshafen, Germany, 9UCSD School of Medicine, La Jolla, CA

    Background/Purpose: Functional impairment among patients with rheumatoid arthritis (RA) can be conceptualized as consisting of a reversible component that relates to disease activity (ACT-HAQ) and…
  • Abstract Number: 1383 • 2012 ACR/ARHP Annual Meeting

    The Burden of Ankylosing Spondylitis and the Cost-Effectiveness of Anti-Tumor Necrosis Factor α Agents in Romania

    Ioan Ancuta1, Catalin Codreanu2, Ruxandra Ionescu3, Magda Parvu4 and Mihai Bojinca1, 1Internal Medicine, “Dr. I. Cantacuzino” Hospital, Bucharest, Romania, 2Rheumatology, “Dr. I. Stoia” Center for Rheumatic Diseases, Bucharest, Romania, 3Internal Medicine, Clinic Hospital Sf. Maria, Bucharest, Romania, 4Internal Medicine, “N.Gh. Lupu” Clinical Hospital, Bucharest, Romania

    Background/Purpose: Ankylosing Spondylitis (AS) usually affects young males, severely impairing their quality of life. Chronic treatment of AS using anti-TNF α agents is costly and…
  • Abstract Number: 373 • 2012 ACR/ARHP Annual Meeting

    Patient-Reported Outcomes in Early Rheumatoid Arthritis Patients Failing to Achieve Stable Low Disease Activity: Comparing Addition of Adalimumab to Methotrexate Monotherapy with Maintenance On Adalimumab Plus Methotrexate

    Arthur Kavanaugh1, Ronald F. van Vollenhoven2, Paul Emery3, James W. Shaw4, Mary A. Cifaldi5, Stefan Florentinus6 and Josef S. Smolen7, 1UCSD School of Medicine, La Jolla, CA, 2Karolinska Institute, Stockholm, Sweden, 3Division of Rheumatic and Musculoskeletal Disease, University of Leeds, Leeds, United Kingdom, 4Global Health Economics and Outcomes Research, Abbott Laboratories, Abbott Park, IL, 5Abbott Laboratories, Abbott Park, IL, 6AbbVie, Rungis, France, 7Division of Rheumatology, Department of Internal Medicine III,, Medical University of Vienna and Hietzing Hospital, Vienna, Austria

    Background/Purpose: Treat-to-target guidelines for rheumatoid arthritis (RA) suggest adjusting therapy every 3-6 months for pts who fail to achieve a disease activity target. However, pts…
  • Abstract Number: 1340 • 2012 ACR/ARHP Annual Meeting

    Effects of Subcutaneous Abatacept or Adalimumab On Remission and Associated Changes in Physical Function and Radiographic Outcomes: One Year Results From the Ample (Abatacept Versus Adalimumab Comparison in Biologic-Naive RA Subjects with Background Methotrexate) Trial

    Roy Fleischmann1, Michael H. Schiff2, Michael E. Weinblatt3, Michael A. Maldonado4, Elena M. Massarotti5 and Yusuf Yazici6, 1Southwestern Medical Center at Dallas, University of Texas, Dallas, TX, 2Rheumatology Division, University of Colorado, Denver, CO, 3Rheumatology & Immunology, Brigham & Women's Hospital, Boston, MA, 4Medical Strategy, Bristol-Myers Squibb, Princeton, NJ, 5Rheumatology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, 6New York University, New York, NY

    Background/Purpose: Advancements in the understanding of Rheumatoid Arthritis (RA) have led to the development of novel therapeutics and treatment guidelines that target remission as an…
  • Abstract Number: 386 • 2012 ACR/ARHP Annual Meeting

    Costs of Tumor Necrosis Factor Blockers Per Treated Rheumatoid Arthritis Patient Using Real-World Drug Data in a US Managed Care Population

    Vernon F. Schabert1, Crystal Watson2, George Joseph2, Paige Iversen1, Chakkarin Burudpakdee1 and David J. Harrison2, 1IMS Health, Alexandria, VA, 2Amgen Inc., Thousand Oaks, CA

    Background/Purpose: Etanercept (ETN), adalimumab (ADA), and infliximab (INF) are FDA-approved tumor necrosis factor (TNF)-blocker treatments for moderate to severe rheumatoid arthritis (RA) and are commonly…
  • Abstract Number: 1303 • 2012 ACR/ARHP Annual Meeting

    Achieving Comprehensive Disease Control in Long-Standing or Early Rheumatoid Arthritis Patients Treated with Adalimumab Plus Methotrexate Versus Methotrexate Alone

    Edward Keystone1, Ferdinand C. Breedveld2, Désirée van der Heijde3, Ronald F. van Vollenhoven4, Stefan Florentinus5, Freddy Faccin6, Shufang Liu7, Hartmut Kupper8 and Arthur Kavanaugh9, 1University of Toronto, Professor of Medicine, Toronto, ON, Canada, 2Dept of Rheumatology C1R, Leiden University Medical Center, Leiden, Netherlands, 3Rheumatology, Leiden University Medical Center, Leiden, Netherlands, 4Karolinska Institute, Stockholm, Sweden, 5AbbVie, Rungis, France, 6Abbott, Abbott Park, IL, 7Immunology Development, Abbott, Abbott Park, IL, 8Immunology Development, Abbott GmbH and Co. KG, Ludwigshafen, Germany, 9UCSD School of Medicine, La Jolla, CA

    Background/Purpose: Effective treatment of rheumatoid arthritis (RA) patients (pts) aims to suppress inflammation, preserve physical function, and prevent structural damage, which together represent the hallmarks…
  • Abstract Number: 369 • 2012 ACR/ARHP Annual Meeting

    Differences in Short-Term Radiographic Progression Following Early Response to Adalimumab Plus Methotrexate Vs. Methotrexate Alone

    Ronald F. van Vollenhoven1, James W. Shaw2, Mary A. Cifaldi3, James Signorovitch4, Eric Q. Wu4, Thomas Samuelson4, Elizabeth Faust4 and Paul Emery5, 1Karolinska Institute, Stockholm, Sweden, 2Global Health Economics and Outcomes Research, Abbott Laboratories, Abbott Park, IL, 3Abbott Laboratories, Abbott Park, IL, 4Analysis Group, Inc., Boston, MA, 5Division of Rheumatic and Musculoskeletal Disease, University of Leeds, Leeds, United Kingdom

    Background/Purpose: To prevent disease progression, treat-to-target recommendations for rheumatoid arthritis (RA) include the evaluation and adjustment of drug therapy at least every 3 months until…
  • Abstract Number: 1304 • 2012 ACR/ARHP Annual Meeting

    Long-Term Use of Adalimumab As Monotherapy Following Attainment of Low Disease Activity with Adalimumab Plus Methotrexate

    Edward Keystone1, Ferdinand C. Breedveld2, Hartmut Kupper3, Shufang Liu4 and Stefan Florentinus5, 1University of Toronto, Professor of Medicine, Toronto, ON, Canada, 2Leiden University Medical Center, Leiden, Netherlands, 3Immunology Development, Abbott GmbH and Co. KG, Ludwigshafen, Germany, 4Immunology Development, Abbott, Abbott Park, IL, 5AbbVie, Rungis, France

    Background/Purpose: There has been increased interest in understanding whether biologics can be safely withdrawn from patients (pts) receiving combination therapy with MTX once a clinical…
  • Abstract Number: 185 • 2012 ACR/ARHP Annual Meeting

    Long-Term Efficacy and Safety of Tumour Necrosis Factor Antagonists for Patients with Behçet’s Disease with Uveitis As Main Involvement

    M. Victoria Hernández1, Marina Mesquida2, Gerard Espinosa3, Victor Llorens2, Laura Pelegrin2, Juan D. Cañete4, Ricard Cervera5, Alfredo M. Adan2 and Raimon Sanmarti1, 1Arthritis Unit. Rheumatology Department, Hospital Clínic of Barcelona, Barcelona, Spain, 2Ophthalmology, Hospital Clínic of Barcelona, Barcelona, Spain, 3Department of Autoimmune Diseases, Hospital Clínic, Barcelona, Barcelona, Spain, 4Rheumatology, Hospital Clínic of Barcelona. IDIBAPS. University of Barcelona, Barcelona, Spain, 5Autoimmune Diseases, Hospital Clínic of Barcelona, Barcelona, Spain

    Background/Purpose: To assess the long-term efficacy and safety of tumour necrosis factor (TNF) antagonists (infliximab [IFX], adalimumab [ADA] and golimumab) for the treatment of patients…
  • Abstract Number: 2598 • 2012 ACR/ARHP Annual Meeting

    Anti-Drug Antibodies Are Associated with Diminished Drug Levels and Treatment Failure

    Miha Kosmac1, Natasa Toplak2, Gabriele Simonini3, Ilaria Pagnini4, Rolando Cimaz5, Vladka Curin Serbec1 and Tadej Avcin5, 1Research and Development Unit, Blood Transfusion Centre of Slovenia, Ljubljana, Slovenia, 2Department of Allergology, Rheumatology and Clinical Immunology, University Children's Hospital Ljubljana Slovenia, Ljubljana, Slovenia, 3Rheumatology Unit-Department of Paediatrics, A. Meyer Children's Hospital, Florence, Italy, 4Rheumatoloy Unit, Anna Meyer Children's Hospital, Department of Pediatrics, University of Florence, Florence, Italy, 5Paediatric Rheumatology International Trials Organization (PRINTO), Istituto Giannina Gaslini, Genova, Italy

    Background/Purpose: Due to their proteinaceus character biologics can often induce an unwanted immune response that results in the formation of anti-drug antibodies in patients receiving…
  • Abstract Number: 1286 • 2012 ACR/ARHP Annual Meeting

    Antibodies to Etanercept and Adalimumab in Rheumatoid Arthritis Inadequate Responders and Clinical Outcomes After an Active Switch to Infliximab

    Chad Pool1, Gopi Shankar2, Allen Schantz2, George Gunn2, Rebecca Bolce3, Marjatta Leirisalo-Repo4, Jim Wang1, John A. Goldman5, Raphael J. DeHoratius6, Roy Fleischmann7 and Dennis Decktor6, 1Janssen Services, LLC, Horsham, PA, 2Janssen R&D, LLC, PA, 3Crescendo Bioscience Inc., South San Francisco, CA, 4Department of Medicine, Division of Rheumatology, Helsinki University Central Hospital, Helsinki, Finland, 5Medical Quarters #293, Atlanta, GA, 6Medical Affairs, Janssen Services, LLC, Horsham, PA, 7Rheumatology, University of Texas Southwestern Medical Center and Metroplex Clinical Research Center, Dallas, TX

    Background/Purpose: To determine if RA patients (pts) who had an inadequate response to etanercept(ETN) or adalimumab(ADA) and developed antibodies (Abs) to ETN or ADA responded…
  • Abstract Number: 5 • 2012 ACR/ARHP Annual Meeting

    Adalimumab Inhibits TNF-Enhanced Human Osteoclast Development More Effectively Than Other Biologic Agents Under in Vitro Conditions of Chronic TNF Exposure

    Bohdan P. Harvey1 and Zehra Kaymakcalan2, 1Biologics, Abbott Laboratories, Worcester, MA, 2Biologics, Abbott, Worcester, MA

    Background/Purpose: TNF-alpha (TNFa) has been shown to contribute to osteoclastogenesis independently and in conjunction with M-CSF or RANKL, two key cytokines involved in osteoclast development. …
  • Abstract Number: 2466 • 2012 ACR/ARHP Annual Meeting

    Pregnancy Outcome in Women Treated with Adalimumab for the Treatment of Rheumatoid Arthritis: The OTIS Autoimmune Diseases in Pregnancy Project

    Christina D. Chambers1, Diana L. Johnson2, Yunjun Luo1, Janina L. Jimenez1, Nicole Mirrasoul1, Elizabeth Salas1, Kenneth Lyons Jones2 and OTIS Research Group3, 1Pediatrics, University of California, San Diego, La Jolla, CA, 2University of California San Diego Department of Pediatrics, La Jolla, CA, 3Pediatrics, La Jolla

    Background/Purpose: The fully human, anti-tumor necrosis factor monoclonal antibody, adalimumab (ADA), is approved for the treatment of rheumatoid arthritis (RA), psoriatic arthritis, ankylosing spondylitis, juvenile…
  • Abstract Number: 1242 • 2012 ACR/ARHP Annual Meeting

    Use of Anti-Tumor Necrosis Factor Therapy Is Associated with Reduced Cardiovascular Event Risk in Rheumatoid Arthritis

    Mike Nurmohamed1, Yanjun Bao2, James Signorovitch3, Parvez M. Mulani4 and Daniel Furst5, 1VU University Medical Center & Jan van Breemen Research Institute, Amsterdam, Netherlands, 2AbbVie, North Chicago, IL, 3Analysis Group, Inc., Boston, MA, 4Abbott Laboratories, Abbott Park, IL, 5Div of Rheumatology, UCLA Medical School, Los Angeles, CA

    Background/Purpose: Rheumatoid arthritis (RA) is associated with increased risks for cardiovascular (CV) comorbidities because of an increased prevalence of traditional CV risk factors and 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.

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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