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Abstracts tagged "drug therapy"

  • Abstract Number: 1595 • 2012 ACR/ARHP Annual Meeting

    Genome-Wide Association Study to High -Throughput Cell-Based Phenotypic Screen Identifies Novel Chemical Inhibitors of CD40 Signaling

    Gang Li1, Dorothee Diogo2, Di Wu1, Jim Spoonamore3, Rheumatoid Arthritis Consortium International (RACI)4, Eli Stahl5, Nicola Tolliday3 and Robert M. Plenge6, 1Division of Rheumatology, Immunology and Allergy and Division of Genetics, Brigham and Women's Hospital, Boston, MA, 2Brigham and Women’s Hospital, Harvard Medical School, Boston, MA, 3Broad Institute, Cambridge, MA, 4Boston, 5Brigham and Women's Hospital, 6Division of Rheumatology, Immunology and Allergy and Division of Genetics, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA

    Background/Purpose: Deriving therapeutic targets from human genetics linked with biological alterations of risk alleles may provide a more successful approach to drug development than traditional…
  • Abstract Number: 1149 • 2012 ACR/ARHP Annual Meeting

    Long-Term Safety of Etanercept in Patients with Juvenile Idiopathic Arthritis (JIA)

    Kirsten Minden1, Martina Niewerth2, Jens Klotsche3, Michael Hammer4, Johannes Peter Haas5, Gerd Ganser6 and Gerd Horneff7, 1Programme Area Epidemiology, German Rheumatism Research Center, a Leibniz Institute, Berlin, Germany, 2Epidemiology, German Rheumatism Research Centre, Berlin, Germany, 3Programme Area Epidemiology, German Rheumatism Research Center, a Leibniz institute, Berlin, Germany, 4Klinik fuer Rheumatologie, St. Josef-Stift, Sendenhorst, Germany, 5German Center for Pediatric and Adolescent Rheumatology, Garmisch-Partenkirchen, Germany, 6Pediatric Rheumatology, Sankt Josef Stift, Sendenhorst, Germany, 7Department of Pediatrics, Centre of Pediatric Rheumatology, Sankt Augustin, Germany

    Background/Purpose: Etanercept (Eta) has been the most frequently used biologic drug in patients with JIA. In Germany, about one in three patients with polyarticular JIA…
  • Abstract Number: 802 • 2012 ACR/ARHP Annual Meeting

    Milnacipran Reduces Brain Activity During Pain in Fibromyalgia

    Anson E. Kairys1, Richard E. Harris2, Eric Ichesco2, Johnson P. Hampson2, Steven Harte2, Daniel J. Clauw3 and Tobias Schmidt-Wilcke2, 1Department of Anesthesiology, Chronic Pain and Fatigue Research Center, University of Michigan, Ann Arbor, MI, 2Anesthesiology, University of Michigan, Ann Arbor, MI, 3Anesthesiology/Internal Medicine (Rheum), University of Michigan, Ann Arbor, MI

    Background/Purpose: Fibromyalgia (FM) is a chronic pain condition characterized by widespread musculoskeletal pain and a number of concomitant symptoms such as fatigue, sleep disturbance, cognitive…
  • Abstract Number: 805 • 2012 ACR/ARHP Annual Meeting

    Milnacipran Increases Cortical to Brainstem Connectivity During Pain in Fibromyalgia

    Eric Ichesco1, Tobias Schmidt-Wilcke1, Anson E. Kairys2, Johnson P. Hampson1, Steven E. Harte1, Daniel J. Clauw3 and Richard E. Harris1, 1Anesthesiology, University of Michigan, Ann Arbor, MI, 2Department of Anesthesiology, Chronic Pain and Fatigue Research Center, University of Michigan, Ann Arbor, MI, 3Anesthesiology/Internal Medicine (Rheum), University of Michigan, Ann Arbor, MI

    Background/Purpose: Fibromyalgia (FM) is a chronic widespread pain disorder characterized by muscle tenderness, fatigue, poor sleep, and mood disturbance.  Milnacipran is a dual serotonin-norepinephrine reuptake…
  • Abstract Number: 642 • 2012 ACR/ARHP Annual Meeting

    Effects of Treatment On the Expression of CCL2 and CXCL10 in Systemic Lupus Erythematosus Patients

    Paul R. Dominguez-Gutierrez1, Angela Ceribelli1, Minoru Satoh2, Eric S. Sobel3, Westley H. Reeves4 and Edward K.L. Chan1, 1Oral Biology, University of Florida, Gainesville, FL, 2Medicine, University of Florida, Gainesville, FL, 3Medicine/Div of Rheumatology, University of Florida, Gainesville, FL, 4Rheumatology & Clinical Imm, University of Florida, Gainesville, FL

     Background/Purpose: Several candidate biomarkers for Systemic Lupus Erythematosus (SLE) have been reported including STAT1, ADAR, CCL2, CXCL10, and miR-146a. This study examines the effects of…
  • Abstract Number: 497 • 2012 ACR/ARHP Annual Meeting

    Golimumab Drug Utilization Patterns in Canada – Higher Retention Rate in Golimumab Treated Rheumatoid Arthritis Patients Compared to Etanercept and Adalimumab

    Hayssam Khalil1 and Amir Tahami2, 1Medical Affairs, Janssen Canada Inc, Toronto, ON, Canada, 2Janssen Canada Inc., Toronto, ON, Canada

    Background/Purpose: Golimumab is a monthly self-injected anti-tumor necrosis factor alpha therapy for patients with rheumatoid arthritis (RA), ankylosing spondylitis (AS), and psoriatic arthritis (PsA). It…
  • Abstract Number: L13 • 2012 ACR/ARHP Annual Meeting

    Apremilast, an Oral Phosphodiesterase 4 Inhibitor, in Patients with Psoriatic Arthritis: Results of a Phase 3, Randomized, Controlled Trial

    Arthur Kavanaugh1, Philip J. Mease2, Juan J. Gomez-Reino3, Adebajo Adewale4, Jürgen Wollenhaupt5, ChiaChi Hu6 and Randall Stevens6, 1UCSD School of Medicine, La Jolla, CA, 2Rheumatology Research, Swedish Medical Center, Seattle, WA, 3Rheumatology, Hospital Clinico Universitario, Santiago, Spain, 4University of Sheffield, Sheffield, United Kingdom, 5Schön Klinik Hamburg Eilbek, Hamburg, Germany, 6Celgene Corporation, Warren, NJ

    Background/Purpose: Apremilast, an oral phosphodiesterase 4 inhibitor, works intracellularly to modulate a network of pro- and anti-inflammatory mediators, including those implicated in the etiopathogenesis of…
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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 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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