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Abstracts tagged "treatment"

  • Abstract Number: 1647 • 2015 ACR/ARHP Annual Meeting

    A Randomized, Clinical Trial to Assess the Relative Efficacy and Tolerability of Two Doses of Etoricoxib in Patients with Rheumatoid Arthritis

    Kara Bickham1, Désirée van der Heijde2, Narinder Rawal3, Joachim Sieper4, Boyd Scott5, Nancy Frontera1, Sandhya Shah1, Paul Stryszak1, Dimitris Papanicolaou1, Zoran Popmihajlov1 and Paul Peloso1, 1Merck & Co., Inc., Kenilworth, NJ, 2University Hospital, Maastricht, Netherlands, 3Orebro University Hospital, Orebro, Sweden, 4Rheumatology, Charite - Campus Benjamin Franklin, Berlin, Germany, 5Merck Sharp & Dohme Corp., Whitehouse Station, NJ

    Background/Purpose: Etoricoxib, a selective cyclooxygenase-2 (COX-2) inhibitor, provides symptom modification in RA patients. Previous dose-ranging studies in RA demonstrated the clinical efficacy of etoricoxib 90…
  • Abstract Number: 1659 • 2015 ACR/ARHP Annual Meeting

    Lack of Effect of Reduced Folic Acid Supplementation on Disease Activity in RA

    Lisa K. Stamp1, Jill Drake2, John L. O'Donnell3, Christopher Frampton4 and Peter T. Chapman5, 1Medicine, University of Otago, Christchurch, Christchurch, New Zealand, 2Rheumatology, Immunology and Allergy, Christchurch Hospital, Christchurch, New Zealand, 3Immunology, Canterbury Health Laboratories, Christchurch, New Zealand, 4University of Otago, Christchurch, Christchurch, New Zealand, 5Rheumatology, Christchurch Hospital, Christchurch, New Zealand

    Background/Purpose: It is recommended that all patients receiving MTX also receive at least 5mg/week of folic acid in an effort to reduce occurrence of MTX…
  • Abstract Number: 2427 • 2014 ACR/ARHP Annual Meeting

    Attainment of Low Disease Activity Is Predictive of Maintenance of Disease Control upon Adalimumab Discontinuation for Two Years Following Combination Therapy in Japanese Patients with Early Rheumatoid Arthritis

    Yoshiya Tanaka1, Hisashi Yamanaka2, Naoki Ishiguro3, Nobuyuki Miyasaka4, Katsuyoshi Kawana5, Katsutoshi Hiramatsu6, Aki Kuroki5 and Tsutomu Takeuchi7, 1University of Occupational and Environmental Health, Japan, Kitakyushu, Japan, 2Institute of Rheumatology, Tokyo Women’s Medical University, Tokyo, Japan, 3Orthopaedic Surgery and Rheumatology, Nagoya University Graduate School of Medicine, Nagoya, Japan, 4Tokyo Medical and Dental University, Tokyo, Japan, 5Abbvie, Tokyo, Japan, 6Medical, Abbvie, Tokyo, Japan, 7Division of Rheumatology, Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan

    Background/Purpose: Although available data has suggested successful withdrawal of a monoclonal antibody TNF blocker after achieving low disease activity (LDA) or remission over the short-term…
  • Abstract Number: 511 • 2014 ACR/ARHP Annual Meeting

    First and Second Line Continuation Rates of Non Anti-TNF-α Biological DMARD for the Treatment of Rheumatoid Arthritis

    Tristan Pascart1, Rene-Marc Flipo2, Xavier Deprez3 and Eric Houvenagel4, 1Rheumatology, Saint-Philibert Hospital, Lille, France, 2Rheumatology, University Hospital Lille, Lille, France, 3Rhumatologie, Ch De Valenciennes, Valenciennes, France, 4Rheumatology, Saint-Philibert Hospital, LOMME, France

    Background/Purpose The 2013 update of the EULAR recommendations for the management of RA with synthetic and biological DMARDs set non-anti-TNF- α as first-line biological treatments.…
  • Abstract Number: 2428 • 2014 ACR/ARHP Annual Meeting

    Comparative Study of Rheumatoid Arthritis Disease Activity Indices in Two Populations of Meteor Database

    Helena Canhão1, Fernando Magalhaes Martins2, Jose Antonio Melo Gomes3, Maria Jose Santos4, Augusto Faustino5, José Antonio Costa6, Cornelia Allaart7, E. Gvozdenovic8, Pedro Machado9, Jaime C. Branco10, João E. Fonseca11 and José Pereira Da-Silva12, 1Av. Prof. Egas Moniz, Hospital Santa Maria, Lisboa, Portugal, 2Portuguese Society of Rheumatology, Lisbon, Portugal, 3Instituto Português de Reumatologia, Lisbon, Portugal, 4Rheumatology, Hospital Garcia de Orta, Almada, Portugal, 5Clínica de Reumatologia de Lisboa, Lisbon, Portugal, 6Rheumatology, Centro Hospitalar do Alto Minho, Hospital de Ponte de Lima, Ponte de Lima, Portugal, 7Rheumatology, Leiden Univ Med Ctr, Leiden, Netherlands, 8Rheumatology, Leiden University Medical Center, Leiden, Netherlands, 9MRC Centre for Neuromuscular Diseases, University College London, London, United Kingdom, 10Rheumatology, Centro Hospitalar de Lisboa Ocidental, Hospital Egas Moniz, Lisboa, Portugal, 11Lisbon Academic Medical Center, Lisbon, Portugal, 12Rheumatology, Hospitais da Universidade de Coimbra, Coimbra, Portugal

    Background/Purpose Our aims were to assess disease activity states using DAS28ESR, CDAI and SDAI and to compare their outcomes in two rheumatoid arthritis (RA) populations…
  • Abstract Number: 497 • 2014 ACR/ARHP Annual Meeting

    Efficacy and Safety Study of a Sequential Therapy of Tocilizumab and, If Initially Inadequately Responded to Tocilizumab, Followed By Rituximab in Patients with Rheumatoid Arthritis and Inadequate Response to Traditional Disease Modifying Anti-Rheumatic Drugs

    Thomas Dörner1, Hans-Peter Tony2, Gerd Burmester1, Hendrik Schulze-Koops3, Jörg Kaufmann4, Peter Kästner5, Herbert Kellner6, Reiner Kurthen7, Sylke Wagner8, Marvin A. Peters9 and Christoph Iking-Konert10, 1Charité - Universitätsmedizin Berlin, Berlin, Germany, 2University Clinic Wuerzburg, Wuerzburg, Germany, 3University Clinic Munich, Munich, Germany, 4Rheumatology Practice, Ludwigsfelde, Germany, 5MVZ Out-patient Rheumatogy Unit Erfurt, Erfurt, Germany, 6Specialist Practice for Rheumatology and Gastroenterology, Munich, Germany, 7Rheumatology Practice, Aachen, Germany, 8Practice for Internal Medicine specialized in Rheumatology, Halle, Germany, 9Roche Pharma AG, Grenzach-Wyhlen, Germany, 10University Clinic Hamburg-Eppendorf, Hamburg, Germany

    Background/Purpose: The MIRAI study evaluated a sequential exposure to 2 defined biologics under rigorous study conditions within a homogeneous population of biological naïve patients (pts)…
  • Abstract Number: 2395 • 2014 ACR/ARHP Annual Meeting

    Understanding Patient Preferences Associated with the Use of Therapies for Rheumatoid Arthritis: Results of a Conjoint Analysis

    K. Saverno1, A. Louder1, A. Singh2, J. Cappelleri3, A. Aten4, A. Koenig5 and M. Pasquale1, 1Comprehensive Health Insights Inc, Louisville, KY, 2Pfizer Inc, Groton, CT, 3Pfizer Inc, New York, NY, 4Humana Inc, Louisville, KY, 5Pfizer Inc, Collegeville, PA

    Background/Purpose: Tofacitinib is an oral Janus kinase inhibitor for the treatment of rheumatoid arthritis (RA). Tofacitinib provides patients with a new oral alternative to biologic…
  • Abstract Number: 378 • 2014 ACR/ARHP Annual Meeting

    The Use of Week 12 CDAI, RAPID3 and DAS28(CRP) Responses to Predict Optimal Response to Methotrexate

    Gerd Burmester1, Gurjit S. Kaeley2, Jeffrey R. Curtis3, Yusuf Yazici4, Benoit Guerette5, Xin Wang5, Alan Friedman5 and Vibeke Strand6, 1Department of Rheumatology and Clinical Immunology, Charité University Medicine, Berlin, Germany, 2College of Medicine, University of Florida, Jacksonville, FL, 3University of Alabama at Birmingham, Birmingham, AL, 4Department of Medicine, Division of Rheumatology, New York University School of Medicine, New York, NY, 5AbbVie, Inc., North Chicago, IL, 6Adjunct, Division of Immunology / Rheumatology, Stanford University, Palo Alto, CA

    Background/Purpose The prediction of treatment outcomes based on early response could guide treatment decisions in patients (pts) with rheumatoid arthritis (RA). The objective was to…
  • Abstract Number: 2406 • 2014 ACR/ARHP Annual Meeting

    Primary Non-Adherence, Associated Clinical Outcomes and Healthcare Resource Utilization Among Rheumatoid Arthritis Patients Prescribed Injectable Biologics

    J. Harnett1, D. Wiederkehr1, R. Gerber2, D. Gruben2, J. Bourret3 and A. Koenig3, 1Pfizer Inc, New York, NY, 2Pfizer Inc, Groton, CT, 3Pfizer Inc, Collegeville, PA

    Background/Purpose: Injectable biologics are commonly used to treat patients (pts) with moderate to severe rheumatoid arthritis (RA); the frequency with which they are prescribed but…
  • Abstract Number: 100 • 2014 ACR/ARHP Annual Meeting

    Evaluation of Real World Experience with Non-Biologic DMARD in the Treatment of RA: Data from an Electronic Health Record Database

    D. Wiederkehr1, J. Harnett1, R. Gerber2, D. Gruben2, E.Y. Mahgoub3, G. Wallenstein1 and A. Koenig3, 1Pfizer Inc, New York, NY, 2Pfizer Inc, Groton, CT, 3Pfizer Inc, Collegeville, PA

    Background/Purpose: Non-biologic (NB) disease-modifying antirheumatic drugs (DMARD) such as methotrexate (MTX) are commonly used to treat rheumatoid arthritis (RA). However, NB‑DMARD can have adverse events…
  • Abstract Number: 2408 • 2014 ACR/ARHP Annual Meeting

    Frequency of Rheumatoid Arthritis Flares in Clinical Practice: Analysis of a Monocentric Cohort of Patients in Stable Remission or Low Disease Activity

    Francesca Ometto1, Costantino Botsios2, Livio Bernardi1, Bernd Raffeiner2,3, Leonardo Punzi4 and Andrea Doria4, 1Rheumatology Unit, Department of Medicine -DIMED, University of Padova, PADOVA, Italy, 2Rheumatology Unit, Department of Medicine - DIMED, University of Padova, Padova, Italy, 3Department of Medicine, Rheumatology - General Hospital Bolzano, Bolzano, Italy, 4Department of Medicine - DIMED, University of Padova, Padova, Italy

    Background/Purpose Rheumatoid arthritis (RA) flares are predictive of structural damage even in case of stable disease course. No definition for flare has been validated to…
  • Abstract Number: 2409 • 2014 ACR/ARHP Annual Meeting

    Omega-3 Fatty Acids and Mediterranean Diet As Complimentary Therapies for Rheumatoid Arthritis

    Ana Carolina Araújo1, Maria Francisca Moraes-Fontes1, Lèlita Santos2 and Nuno Riso1, 1Serviço de Medicina 2, Hospital de Curry Cabral, Centro Hospitalar Lisboa Central, Lisbon, Portugal, 2Serviço de Medicina Interna, Centro Hospitalar Universitário de Coimbra, Coimbra, Portugal

    Background/Purpose Rheumatoid arthritis (RA) is a chronic inflammatory disease affecting the synovial joints, often with a progressive and destructive course, leading to disability. Nowadays, there…
  • Abstract Number: 1972 • 2014 ACR/ARHP Annual Meeting

    Analysis of Anakinra in Primary Human Cell Systems Reveals an in Vitro Signature for Skin-Related Side Effects

    Ellen L. Berg, Alison O'Mahony and Mark A Polokoff, BioSeek, South San Francisco, CA

    Background/Purpose The therapeutic options for treatment of rheumatic diseases have grown and now include a variety of inflammatory pathway inhibitors, with diverse mechanisms, but having…
  • Abstract Number: 1529 • 2014 ACR/ARHP Annual Meeting

    Evaluation of the Pharmacokinetics and Safety of the Interactions Between the Anti-Interleukin-6 Monoclonal Antibody Sirukumab and Cytochrome P450 Activities in Patients with Rheumatoid Arthritis

    Dick de Vries, Yanli Zhuang, Stanley Marciniak, Zhenhua Xu, Dion Chen, Hugh M. Davis, Honghui Zhou and Francisco Leon, Janssen Research & Development, LLC., Spring House, PA

    Background/Purpose: Interleukin 6 (IL-6) reduces the expression of cytochrome P450 (CYP) enzymes. The goal of the study was to evaluate: 1) the effect of sirukumab…
  • Abstract Number: 1512 • 2014 ACR/ARHP Annual Meeting

    Therapeutic Efficacy of a Novel Oral Small Molecule Macrophage Migration Inhibitory Factor [MIF] Inhibitor: A Promising Safe & Efficacious Treatment for Rheumatoid Arthritis

    Anderson Gaweco1,2, Samantha Palmer2, Rambon Shamilov2, Caroline Stremnitzer2, Michael Fisher2, Gregg Crichlow2, William Windsor2, Ellen M. Ginzler3 and Jefferson Tilley2, 1SUNY-Downstate Medical Center, Brooklyn, NY, 2Innovimmune Biotherapeutics, Brooklyn, NY, 3Rheumatology, SUNY-Downstate Medical Center, Brooklyn, NY

    Background/Purpose: Macrophage migration inhibitory factor [MIF] is a cytokine secreted by activated T cells and macrophages that plays an important role in RA and autoimmune…
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Embargo Policy

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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