ACR Meeting Abstracts

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Abstracts tagged "safety and tumor necrosis factor (TNF)"

  • Abstract Number: 218 • 2018 ACR/ARHP Annual Meeting

    Risk of Serious Infection Associated with TNF Inhibitor Versus Triple Therapy in Rheumatoid Arthritis Patients

    Yinzhu Jin1, Eun Ha Kang2, Rishi J. Desai3, Angela Tong1 and Seoyoung C. Kim4,5, 1Division of Pharmacoepidemiology and Pharmacoeconomics, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, 2Division of Rheumatology, Department of Internal Medicine, Seoul National University Bundang Hospital, Gyeonggi-do, Korea, Republic of (South), 3Division of Pharmacoepidemiology and Pharmacoeconimics, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, 4Division of Pharmacoepidemiology and Pharmocoeconomics, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, 5Rheumatology, Immunology and Allergy, Brigham and Women’s Hospital, Boston, MA

    Background/Purpose: Treatment with tumor necrosis factor inhibitor (TNFi) with methotrexate or triple therapy (MTX, sulfasalazine, and sulfasalazine) is considered in patients with rheumatoid arthritis (RA)…
  • Abstract Number: 526 • 2017 ACR/ARHP Annual Meeting

    Comparative Pulmonary Safety of Abatacept and Tumor Necrosis Factor Inhibitors in Patients with RA and Chronic Pulmonary Condition

    Eun Ha Kang1, Yinzhu Jin2, Sara Dejene3, Gregory Brill3, Rishi J. Desai2, Jeffrey A. Sparks4 and Seoyoung C. Kim5, 1Division of Rheumatology, Department of Internal Medicine, Division of Rheumatology, Department of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, Korea, Republic of (South), 2Division of Pharmacoepidemiology and Pharmacoeconomics, Brigham and Women’s Hospital, Boston, MA, 3Brigham and Women's Hospital, Boston, MA, 4Rheumatology, Immunology and Allergy, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, 5Rheumatology, Immunology and Allergy; Pharmacoepidemiologyand Pharmacoeconomics, Brigham and Women's Hospital, Boston, MA

    Background/Purpose: Patients with rheumatoid arthritis (RA) can have various pulmonary comorbidities including asthma, chronic obstructive pulmonary disease (COPD) and interstitial lung disease (ILD). Biologics can…
  • Abstract Number: 547 • 2017 ACR/ARHP Annual Meeting

    Long-Term Risk of Serious Infections in Patients with Rheumatoid Arthritis Treated with Rituximab: 5 Year Data from the British Society for Rheumatology Biologics Register for Rheumatoid Arthritis

    Diederik De Cock1, Lianne Kearsley-Fleet1, Lucía Silva Fernández2, Mark Lunt1, Kath Watson1, Deborah P.M. Symmons1,3 and Kimme L. Hyrich1,3, 1Arthritis Research UK Centre for Epidemiology, University of Manchester, Manchester Academic Health Science Centre, Manchester, United Kingdom, 2Arthritis Research UK Centre for Epidemiology, Centre for Musculoskeletal Research, Manchester Academic Health Science Centre, The University of Manchester, Manchester, United Kingdom, 3National Institute of Health Research Manchester Musculoskeletal Biomedical Research Centre, Central Manchester NHS Foundation Trust, Manchester Academic Health Science Centre, Manchester, United Kingdom

    Background/Purpose: In the United Kingdom (UK), rituximab (RTX) or a second tumour necrosis factor inhibitor (TNFi) are both permitted treatment options for patients with rheumatoid…
  • Abstract Number: 967 • 2015 ACR/ARHP Annual Meeting

    Safety, Tolerability, and Pharmacodynamics of ABT-122, a Dual TNF- and IL-17-Targeted Dual Variable Domain (DVD)-IgTM in Subjects with Rheumatoid Arthritis

    Roy Fleischmann1, Frank Wagner2, Alan J. Kivitz3, Heikki T. Mansikka4, Nasser Khan4, Jia Liu4, Jacob Gagnon4, Feng Hong5, Melanie Ruzek4 and Robert J. Padley4, 1University of Texas Southwestern Medical Center at Dallas, Dallas, TX, 2Charité Research Organisation GmbH, Berlin, Germany, 3Altoona Center for Clinical Research, Duncansville, PA, 4AbbVie Inc., North Chicago, IL, 5AbbVie Inc., Worcester, MA

    Background/Purpose: TNF and IL-17 independently contribute to the pathophysiology of rheumatoid arthritis (RA) acting synergistically to induce mediators of inflammation and joint destruction. Selective dual…
  • Abstract Number: 951 • 2014 ACR/ARHP Annual Meeting

    Safety, Tolerability, and Functional Activity of ABT-122, a Dual TNF- and IL-17A–Targeted DVD-Ig™, Following Single-Dose Administration in Healthy Subjects

    Heikki Mansikka1, Melanie Ruzek2, Margaret Hugunin2, Alexander Ivanov2, Alyssa Brito2, Anca Clabbers2, Carolyn Cuff3, Chung-Ming Hsieh2, Martin Okun1, Renee Heuser1, David Carter1, Barbara Hendrickson1, Dipak Pisal1, Sandra Goss1, Jia Liu1, Charles Locke1, Nasser Khan1 and Robert Padley1, 1AbbVie, Inc, North Chicago, IL, 2AbbVie, Inc, Worcester, MA, 3Immunology, AbbVie, Inc, Worcester, MA

    Background/Purpose: Several lines of evidence indicate that greater clinical efficacy and protection of joints may be possible in patients with RA by neutralizing TNF and…
  • Abstract Number: 2549 • 2012 ACR/ARHP Annual Meeting

    Induction of Remission in Patients with up to 12 Months of Moderate-to-Severe Rheumatoid Arthritis Symptoms Treated with Etanercept Plus Methotrexate Over 52 Weeks

    Paul Emery1, Mohammed Hamoudeh2, Oliver FitzGerald3, Bernard Combe4, Stefanie Gaylord5, Theresa Williams5, Jack Bukowski6, Ronald Pedersen5, Andrew S. Koenig7 and Bonnie Vlahos5, 1Department of Rheumatology, Leeds General Infirmary, Leeds, United Kingdom, 2Department of Medicine - Rheumatology, Hamad Medical Corporation, Doha, Qatar, 3Department of Rheumatology, St.Vincent's University Hospital, Dublin, Ireland, 4Department of Rheumatology, Lapeyronie Hospital, Montpellier, France, 5Department of Specialty Care, Pfizer Inc., Collegeville, PA, 6Department of Specialty Care, Pfizer Inc, Collegeville, PA, 7Pfizer, Inc., Collegeville, PA

    Background/Purpose: In the COMET study, etanercept (ETN) plus methotrexate (MTX) therapy in patients with early rheumatoid arthritis (RA) yielded high clinical remission rates,1 but whether…
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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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