ACR Meeting Abstracts

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Abstracts tagged "drug therapy"

  • 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…
  • Abstract Number: 2270 • 2012 ACR/ARHP Annual Meeting

    The DNA Methylome of Systemic Lupus Erythematosus (SLE) From Whole Peripheral Blood Mononuclear Cells (PBMCs)

    Robert Shoemaker1, Lou H. Bookbinder2, David L. Boyle3, Gary S. Firestein4, Jonathan E. Lim5 and David W. Anderson6, 1Bioinformatics, NexDx, Inc., San Diego, CA, 2Molecular Biology, NexDx, Inc., San Diego, 3Div of Rheum, UCSD School of Medicine, La Jolla, CA, 4Div of Rheumatology, UCSD School of Medicine, La Jolla, CA, 5Research and Development, NexDx, Inc., San Diego, 6Research and Development, NexDx, Inc., San Diego, CA

    Background/Purpose:  SLE is a disease where epigenetic mechanisms play a role. Methylation of DNA at CpG loci is known to influence the suppression or activation…
  • Abstract Number: 1909 • 2012 ACR/ARHP Annual Meeting

    Use of Uric Lowering Therapies within a Large Health Care System

    Robert A. Overman1, Brian F. Mandell2 and Chad L. Deal3, 1Rheumatology, Cleveland Clinic Foundation, Cleveland, OH, 2Dept of Rheum/Immun NA10, The Cleveland Clinic, Cleveland, OH, 3Dept of Rheum & Imm Dis /A 50, Cleveland Clinic, Cleveland, OH

    Background/Purpose: Guidelines for initiating urate lowering therapy (ULT) in the treatment of gout recommend treatment to a target serum urate (SUA) level of ≤6mg/dl with…
  • Abstract Number: 1895 • 2012 ACR/ARHP Annual Meeting

    Safety Competences Knowledge and Behavioural Skills of Patients Treated by Biologics in Rheumatology

    Anne-Christine Rat1, Bruno Fautrel2, Elisabeth Flipon3, Laure Gossec4, Benoit-Damien Caritey5, Laurent Marguerie6, Henri Nataf7, Beatrice Pallot Prades8, Rose Marie Poilvert9, Valerie Royant10, Fathia Sadji11, Christelle Sordet12, Corinne Thevenot13 and Catherine Beauvais14, 1CHU Nancy, Clinical Epidemiology and Evaluation, Université de Lorraine, Paris Descartes University, APEMAC, EA 4360, Nancy, France, 2Rheumatology / GRC08-EEMOIS, APHP-Pitie Salpetriere Hospital / UPMC, Paris, France, 3Cochin hospital, Paris, France, 4Rheumatology B Department, Paris-Descartes University, Cochin Hospital, Paris, France, 5Epidemiology, Université de lorraine, Nancy, France, 6Rheumatology department, Institut Calot, Berck, France, 7Mantes-la-Jolie, Mantes-la-Jolie, France, 8Rheumatology department, Saint Etienne university hospital, Saint Etienne, France, 9Rheumatology department, Saint Antoine Hospital, Paris, France, 10Chartres, Chartres, 11Rheumatology department, Victor Jousselin Hospital, Dreux, France, 12Rheumatology, Strasbourg University Hospital, Strasbourg, France, 13Department of Internal Medicine, Laon hospital, Laon, France, 14Rhumatologie, Saint Antoine, Paris, France

    Background/Purpose: Biologics are known to entail specific risks; therefore teaching patients safety skills, appropriate behaviours in situations of risks and what decisions to take in…
  • Abstract Number: 1715 • 2012 ACR/ARHP Annual Meeting

    Imatinib Mesylate (Gleevec™) in the Treatment of Diffuse Cutaneous Systemic Sclerosis: Results of a 24 Month Open Label, Extension Phase

    Jessica K. Gordon1, Morgana L. Davids2, Kamini Doobay2, Jamie N. Mersten1, Cynthia Magro3, Horatio F. Wildman4, Stephen L. Lyman5, Mary K. Crow6 and Robert F. Spiera1, 1Rheumatology, Hospital for Special Surgery, New York, NY, 2Medicine/Rheumatology, Hospital for Special Surgery, New York, NY, 3Dermatopathology, Weill-Cornell Medical Center, New York, NY, 4Dermatology, Weill-Cornell Medical Center, New York, NY, 5Research, Hospital for Special Surgery, New York, NY, 6Department of Medicine, Hospital for Special Surgery, New York, NY

    Background/Purpose: Imatinib mesylate (IM) has been shown to decrease fibrosis in preclinical models and is a treatment of interest for Systemic Sclerosis (SSc).   We have…
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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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