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Abstracts tagged "DMARDs"

  • Abstract Number: 1669 • 2012 ACR/ARHP Annual Meeting

    Infection Risk After Orthopaedic Surgery in Patients with Inflammatory Rheumatic Diseases, with Focus On Discontinuation of TNF-Alpha-Inhibitors

    Catrina B. Scherrer1, Anne AF Mannion2, Diego Kyburz3, Markus Vogt4 and Ines A. Kramers-de Quervain1, 1Rheumatology, Schulthess Clinic, Zürich, Switzerland, 2Research Department, Schulthess Clinic, Zürich, Switzerland, 3Department of Rheumatology, University Hospital of Zurich, Zurich, Switzerland, 4Infectious Diseases Service, Cantonal Hospital Zug, Baar, Switzerland

    Background/Purpose: Infections after orthopaedic surgeries are feared complications, leading to costly treatments and successive interventions. A higher postoperative infection risk is discussed in patients with…
  • Abstract Number: 833 • 2012 ACR/ARHP Annual Meeting

    A Phase 1, Randomized, Double-Blind, Placebo-Controlled Multiple-Dose Study of Intravenous Staphylococcal Protein A in Patients with Active Rheumatoid Arthritis On Methotrexate: Safety, Pharmacokinetics and Efficacy

    Edward Bernton1, Eduard Krantz2 and William Gannon Jr.3, 1Protalex Inc., Summit, NJ, 2Parexel Clinical Pharmacology, Bloemfontein, South Africa, 3Capital City Technical Consulting, Inc., Washington, DC

    Background/Purpose: PRTX-100 is highly-purified GMP staphylococcal protein A (SpA) that binds with extremely high affinity to the Vh antibody framework region of Clade Vh3 immunoglobulins. …
  • Abstract Number: 2545 • 2012 ACR/ARHP Annual Meeting

    A Randomized, Double-Blind, Parallel Group Study of the Safety and Efficacy of Tocilizumab SC Versus Tocilizumab IV, in Combination with Traditional Dmards in Patients with Moderate to Severe RA

    G. R. Burmester1, Andrea Rubbert-Roth2, Alain G. Cantagrel3, Stephen Hall4, Piotr Leszczynski5, Daniel Feldman6, Madura J. Rangaraj7, Georgia Roane8, Charles L. Ludivico9, Francesco Ramirez10 and Min Bao11, 1Charité-Universitätsmedizin Berlin, Berlin, Germany, 2Klinikum der Universität zu Köln, Köln, Germany, 3Dept of Rheumatology, Centre Hospitalier Universitaire de Toulouse, Toulouse, France, 4Cabrini Medical Centre, Malvern, Australia, 5Dept. of Rheumatology and Clinical Immunology, J. Strus Poznan Municipal Hospital, Poznan University of Medical Sciences, Poznan, Poland, 6Rheumatology, Universidade Federal de de São Paulo, Sao Paulo, Brazil, 7Arthritis & Diabetes Clinic, Inc., Monroe, LA, 8Rheumatology Associates of South Carolina, Charleston, SC, 9East Penn Rheumatology Assoc, Bethlehem, PA, 10Roche Products Limited, Welwyn, United Kingdom, 11Genentech, South San Francisco, CA

    Background/Purpose: The objective of this study was to compare the efficacy and safety of tocilizumab (TCZ) subcutaneous (SC) and TCZ intravenous (IV) regimen in patients…
  • Abstract Number: 1560 • 2012 ACR/ARHP Annual Meeting

    What Will Determine Adherence to Pharmaceutical Treatment for Rheumatoid Arthritis? A Systematic Review

    Annelieke Pasma1, Adriaan van 't Spijker2, Jan van Busschbach3, Johanna M.W. Hazes4 and Jolanda J. Luime5, 1Rheumatology, Erasmus MC University Medical Center, Rotterdam, Netherlands, 2Psychiatry, section Medical Psychology and Psychotherapy, Erasmus MC University Medical Center, Rotterdam, Netherlands, 3Medical Psychology and Psychotherapy, Erasmus MC - University Medical Center, Rotterdam, Netherlands, 4Rheumatology, Erasmus MC, Rotterdam, Netherlands, 5Rheumatology, Erasmus University Medical Center, Rotterdam, Netherlands

    Background/Purpose: In the early stages of Rheumatoid Arthritis (RA), adherence to the prescribed treatment is important to prevent irreversible joint damage. However, medication adherence rates…
  • Abstract Number: 773 • 2012 ACR/ARHP Annual Meeting

    Remission Rates with Tofacitinib Treatment in Rheumatoid Arthritis: A Comparison of Various Remission Criteria

    Josef S. Smolen1, D. Aletaha2, D. Gruben3, J. D. Bradley4, S. H. Zwillich3, S. Krishnaswami3, B. Benda5 and C. Mebus6, 1Division of Rheumatology, Department of Internal Medicine III,, Medical University of Vienna, Vienna, Austria, 2Department of Internal Medicine 3, Division of Rheumatology, Medical University of Vienna, Vienna, Austria, 3Pfizer Inc., Groton, CT, 4Worldwide Pharmaceutical Development, Pfizer Inc., Groton, CT, 5Clinical Development & Medical Affairs, Pfizer Inc., Collegeville, PA, 6Pfizer Inc, Groton, CT

    Background/Purpose: Tofacitinib is a novel, oral Janus kinase inhibitor being investigated as a targeted immunomodulator and disease-modifying therapy for RA. This analysis evaluated the rates…
  • Abstract Number: 2486 • 2012 ACR/ARHP Annual Meeting

    Radiographic, Clinical and Functional Comparison of Tofacitinib Monotherapy Versus Methotrexate in Methotrexate-Naïve Patients with Rheumatoid Arthritis

    Eun Bong Lee1, Roy Fleischmann2, Stephen Hall3, Ronald F. van Vollenhoven4, John Bradley5, David Gruben6, Tamas Koncz7, Sriram Krishnaswami5, Gene Wallenstein6, Samuel H. Zwillich5, Bethanie E. Wilkinson6 and the ORAL Start Investigators8, 1Seoul National University, Seoul, South Korea, 2Metroplex Clinical Research Center, Dallas, TX, 3Cabrini Medical Centre, Melbourne, Australia, 4Karolinska Institute, Stockholm, Sweden, 5Pfizer Inc, Groton, CT, 6Pfizer Inc., Groton, CT, 7Pfizer Inc., New York, NY, 8Groton, CT

    Background/Purpose: Tofacitinib is a novel, oral Janus kinase inhibitor being investigated as a targeted immunomodulator and disease-modifying therapy for RA. This Phase 3, 24-mo study (ORAL…
  • Abstract Number: 1573 • 2012 ACR/ARHP Annual Meeting

    Baseline Screening Recommendations for Rheumatoid Arthritis Patients Treated with Disease Modifying Anti-Rheumatic Drugs:  Does an Educational Intervention Change Practice in an Outpatient Clinic?

    Debra C. Lloyd1, John N. Mecchella2 and Daniel Albert3, 1Rheumatology, Dartmouth-Hitchcock Med Ctr, Lebanon, NH, 2Rheumatology, Dartmouth Hitchcock Medical Center, Lebanon, NH, 3Rheumatology, Dartmouth-Hitchcock Medical Center, Geisel School of Medicine, Lebanon, NH

    Background/Purpose: In 2008, the American College of Rheumatology (ACR) developed recommendations for use of non-biologic and biologic DMARDs in the treatment of rheumatoid arthritis (RA). …
  • Abstract Number: 566 • 2012 ACR/ARHP Annual Meeting

    Effect of TNF Antagonists On Radiographic Progression in Psoriatic Arthritis: Systematic Review and Meta-Analysis of Randomized Controlled Trials

    Radjiv Goulabchand1, Gael Mouterde1, Cédric Lukas2, Thomas Barnetche3, Jacques Morel1 and Bernard Combe1, 1Rheumatology, Montpellier 1 University, Lapeyronie Hospital, Montpellier, France, 2Immuno-Rhumatologie, Hopital Lapeyronie, Montpellier, France, 3Rheumatology, CHU Bordeaux Pellegrin, Bordeaux, France

    Background/Purpose: Psoriatic arthritis (PsA) can cause important structural damages which can lead to disability. TNF antagonists have shown their clinical efficacy in PsA, but only…
  • Abstract Number: 2490 • 2012 ACR/ARHP Annual Meeting

    Herpes Zoster and Tofacitinib Therapy in Patients with Rheumatoid Arthritis

    K. L. Winthrop1, H. Valdez2, E. Mortensen3, R. Chew4, S. Krishnaswami5, T. Kawabata5 and R. Riese4, 1Division of Infectious Diseases, Oregon Health and Science University, Portland, OR, 2Pfizer Inc., New York, NY, 3Global Medical Affairs, Pfizer Inc., Collegeville, PA, 4Pfizer Inc., Groton, CT, 5Pfizer Inc, Groton, CT

    Background/Purpose: Patients (pts) with RA are at increased risk for herpes zoster (HZ) i.e. ‘shingles'. Tofacitinib, a novel oral Janus kinase inhibitor investigated as a…
  • Abstract Number: 1297 • 2012 ACR/ARHP Annual Meeting

    Tofacitinib and Adalimumab Achieve Similar Rates of Low Disease Activity in Rheumatoid Arthritis — Lack of Improvement in Disease Activity Score by 3 Months Predicts Low Likelihood of Low Disease Activity At 1 Year

    Ronald F. van Vollenhoven1, Sriram Krishnaswami2, Birgitta Benda3, David Gruben4, Bethanie Wilkinson4, Charles A. Mebus4, Samuel H. Zwillich2 and John Bradley2, 1Karolinska Institute, Stockholm, Sweden, 2Pfizer Inc, Groton, CT, 3Pfizer Inc., Collegeville, PA, 4Pfizer Inc., Groton, CT

    Background/Purpose: Tofacitinib is a novel oral Janus kinase inhibitor being investigated as a targeted immunomodulator and disease-modifying therapy for RA. This post-hoc analysis of the…
  • Abstract Number: 491 • 2012 ACR/ARHP Annual Meeting

    Predictors of Initiating Biologic Monotherapy in Biologic Naïve Patients with Rheumatoid Arthritis (RA) in a US Registry Population

    Dimitrios A. Pappas1, George W. Reed2, Ani John3, Ashwini Shewade3, Katherine C. Saunders4, Jenny Devenport5, Jeffrey D. Greenberg6 and Joel M. Kremer7, 1Columbia University, New York, NY, 2University of Massachusetts Medical School, Worcester, MA, 3Genentech Inc., South San Francisco, CA, 4Corrona, LLC., Southborough, MA, 5Genentech, South San Francisco, CA, 6Rheumatology, NYU Hospital for Joint Diseases, New York, NY, 7Albany Medical College and The Center for Rheumatology, Albany, NY

    Background/Purpose: Published data have shown that approximately one-third of patients with RA are treated with biologic (Bio) monotherapy (MT) (without concomitant DMARD) and a considerable…
  • Abstract Number: 2480 • 2012 ACR/ARHP Annual Meeting

    Disease-Modifying Antirheumatic Drug Use and Toxicities Among Elderly Patients with Rheumatoid Arthritis

    Rebecca L. Manno1, Dimitrios A. Pappas2, Katherine C. Saunders3, George Reed4, Shannon Grant5 and Clifton O. Bingham III6, 1Division of Rheumatology, Johns Hopkins University, Baltimore, MD, 2New York Presbyterian Hospital, Columbia University, College of Physicians & Surge, New York, NY, 3Corrona, LLC., Southborough, MA, 4Division of Behavioral and Preventive Medicine, University of Massachusetts Medical School, Worcester, MA, 5Axio Research LLC, Seattle, WA, 6Department of Medicine, Johns Hopkins University, Baltimore, MD

    Background/Purpose: The aging population has resulted in large numbers of older individuals requiring treatment for rheumatoid arthritis (RA). We sought to describe the clinical characteristics…
  • Abstract Number: 1298 • 2012 ACR/ARHP Annual Meeting

    Improvement of Treatment Outcome of Rheumatoid Arthritis with Salazosulfapyridine by Pharmacogenetic Approach

    Shunichi Kumagai1, Yoshiaki Hagiwara2, Yoshihide Ichise1, Sho Sendo3, Nobuhiko Okada1, Jun Saegusa4 and Goh Tsuji5, 1Center of rheumatic diseases, Shinko hospital, Kobe, Japan, 2Department of Evidence-Based Laboratory Medicine, Kobe University Graduate School of Medicine, Kobe, Japan, 3Center of rheumatic diseases, Shinko Hospital, Kobe, Japan, 4Rheumatology and Clinical Immunology, Kobe University Graduate School of Medicine, Kobe, Japan, 5Center for Rheumatic Diseases, Shinko Hospital, Kobe, Japan

    Background/Purpose: Salazosulfapyridine (SASP) is acetylated in liver by N-acetyltransferase2 (NAT2) in the track of metabolism. Previous studies have shown that genotyping of NAT2 is adequate…
  • Abstract Number: 473 • 2012 ACR/ARHP Annual Meeting

    The Addition of Another Disease-Modifying Anti-Rheumatic Drug to Methotrexate in Place of Infliximab Reduces the Flare Rate During 2 Years After Infliximab Discontinuation in Patients with Rheumatoid Arthritis

    Hideto Kameda1, Takahiko Kurasawa1, Hayato Nagasawa2, Koichi Amano3 and Tsutomu Takeuchi4, 1Division of Rheumatology, Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan, 2Division of Rheumatology and Clinical Immunology, Department of Internal Medicine, Saitama Medical Ctr, Kawagoe, Japan, 3Department of Rheumatology and Clinical Immunology, Saitama Medical Center, Saitama Medical University, Saitama, Japan, 4Rheumatology, Keio University School of Medicine, Tokyo, Japan

    Background/Purpose: The treatment strategy for rheumatoid arthritis (RA) should be divided into remission-induction phase and its maintenance phase. To date, the usefulness of the combination…
  • Abstract Number: 2485 • 2012 ACR/ARHP Annual Meeting

    Tofacitinib, an Oral Janus Kinase Inhibitor: Analyses of Efficacy and Safety of 10 versus 5mg Twice Daily in a Pooled Phase 3 and Long-Term Extension Rheumatoid Arthritis Population

    S. Cohen1, S. Krishnaswami2, B. Benda3, R. Riese2, M.G. Boy4, D. Gruben4, G. Wallenstein5, C. A. Mebus4, S. H. Zwillich2 and J. D. Bradley6, 1Metroplex Clinical Research Centre, Dallas, TX, 2Pfizer Inc., Groton, CT, 3Clinical Development & Medical Affairs, Pfizer Inc., Collegeville, PA, 4Pfizer Inc, Groton, CT, 5Pfizer Inc, New York, NY, 6Worldwide Pharmaceutical Development, Pfizer Inc., Groton, CT

    Background/Purpose: Tofacitinib is a novel, oral Janus kinase inhibitor being investigated as a targeted immunomodulator and disease-modifying therapy for RA. Phase (P) 3 studies demonstrated…
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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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