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Abstracts tagged "Biologics"

  • Abstract Number: 1943 • 2014 ACR/ARHP Annual Meeting

    In Vivo Effects of Epratuzumab, a Monoclonal Antibody Targeting Human CD22, on B Cell Function in Human CD22 Knock-in (Huki) Mice

    Carolin Brandl*1, Lamia Özgör*1, Miriam Wöhner1,2, Anthony Shock3 and Lars Nitschke1, 1Division of Genetics, University of Erlangen, Erlangen, Germany, 2Research Institute of Molecular Pathology, Vienna, Austria, 3UCB Pharma, Slough, United Kingdom

    Background/Purpose Epratuzumab is a humanized monoclonal antibody that targets the B cell-specific protein CD22 currently in Phase 3 clinical trials in patients (pts) with systemic…
  • Abstract Number: 1358 • 2014 ACR/ARHP Annual Meeting

    A Systematic Analysis of the Safety of Prescribing Anti-Rheumatic Immunosuppressive and Biologic Drugs in Pregnant Women

    Sonia Panchal1, Julia Flint2, Maud van de Venne3, Madeline Piper4, Alice Hurrel5, Joel Cunningham5, Mary Gayed6, Karen Schreiber7, Subha Anthanari8, Mohamed Nisar8, David Williams9, Munther Khamashta10, Caroline Gordon11 and Ian Giles2, 1Rheumatology, University Hospitals of Leicester NHS Trust, Leicester, United Kingdom, 2UCL Division of Medicine, University College London, London, United Kingdom, 3Obstetrics and Gynaecology, North Bristol NHS Trust, Bristol, United Kingdom, 4Ysbyty Ystrad Fawr, Aneurin Bevan Health Board Wales, Wales, United Kingdom, 5Institute for Women's Health, University College London, London, United Kingdom, 6Rheumatology Division of Infection and Immunity, The Medical School, University of Birmingham, Birmingham, United Kingdom, 7Lupus Research Unit, Division of Infection and Immunity, Guy's and St Thomas' NHS Foundation Trust, London, United Kingdom, 8Rheumatology, Burton Hospitals NHS Foundation Trust, Burton-upon-Trent, United Kingdom, 9University College London, London, United Kingdom, 10Lupus Research Unit, Division of Women's Health, Guy's and St Thomas' NSH Foundation Trust, London, United Kingdom, 11Rheumatology, Division of Infection and Immunity, The Medical School, University of Birmingham, Birmingham, United Kingdom

    Background/Purpose The use of anti-rheumatic drugs in pregnancy is often complicated by concerns over their potential for adverse effects. Given that rheumatic diseases often affect…
  • Abstract Number: 518 • 2014 ACR/ARHP Annual Meeting

    Risk of Infection Associated with Subsequent Biologic Use Following Rituximab—Results from a National RA Patient Registry

    Leslie R. Harrold1, George W. Reed1,2, Chitra Karki3, Robert Magner1, Ashwini Shewade4, Ani John4, Joel M. Kremer5 and Jeffrey D. Greenberg3,6, 1University of Massachusetts Medical School, Worcester, MA, 2Corrona, LLC., Southborough, MA, 3Corrona, LLC, Southborough, MA, 4Genentech, Inc, South San Francisco, CA, 5Albany Medical College and The Center for Rheumatology, Albany, NY, 6NYU School of Medicine, New York, NY

    Background/Purpose: Rituximab is a chimeric monoclonal antibody for the treatment of rheumatoid arthritis (RA). Prolonged B-cell depletion from repeated doses of rituximab may be associated…
  • Abstract Number: 2938 • 2014 ACR/ARHP Annual Meeting

    A Randomized, Double-Blind, Placebo-Controlled, 16-Week Study of Subcutaneous Golimumab in Patients with Active Nonradiographic Axial Spondyloarthritis

    J Sieper1, D van der Heijde2, M Dougados3, Walter P. Maksymowych4, J Boice5, G Bergman5, S Curtis5, A Tzontcheva5, S Huyck5 and HH Weng5, 1University Clinic Benjamin Franklin, Berlin, Germany, 2Leiden University Medical Center, Leiden, Netherlands, 3Paris-Descartes University, Paris, France, 4Department of Medicine, University of Alberta, Alberta, AK, 5Merck & Co., Inc., Whitehouse Station, NJ

    Background/Purpose Axial spondyloarthritis (axSpA), including ankylosing spondylitis and nonradiographic axial SpA (nr-axSpA), is a chronic inflammatory disease marked by back pain and progressive spinal stiffness.…
  • Abstract Number: 1853 • 2014 ACR/ARHP Annual Meeting

    Persistence and Predictors of Biologic TNFi Therapy Among Biologic naïve Psoriatic Arthritis Patients in a US Registry

    Philip J. Mease1, David Collier2, Chitra Karki3, Guo Li4, Bojena Bitman5 and Jeffrey D. Greenberg3,6, 1Director, Rheumatology Research, Swedish Medical Center, Seattle, WA, 2Amgen, Inc., Thousand Oaks, CA, 3Corrona, LLC., Southborough, MA, 4Axio Research LLC, Seattle, WA, 5Amgen, Inc., San Francisco, CA, 6Rheumatology, New York University School of Medicine, New York, NY

    Background/Purpose: Registry data regarding biologic DMARD therapy as a mono or combo (combined with a traditional oral DMARD) in subjects with Psoriatic Arthritis (PsA) are…
  • Abstract Number: 1153 • 2014 ACR/ARHP Annual Meeting

    Area of Residence and Socio-Economic Factors Significantly Affect Access to Biological Therapy for Rheumatoid Arthritis Patients in Romania

    Catalin Codreanu1, Corina Mogosan2, Ruxandra Ionescu3, Ioan Ancuta4, Magda Parvu5 and Simona Rednic6, 15 Thomas Masaryk Street, 'Dr. Ion Stoia' Clinical Center of Rheumatic Diseases, Bucharest, Romania, 2'Dr. Ion Stoia' Clinical Center of Rheumatic Diseases, Bucharest, Romania, 3Rheumatology, Sfanta Maria Clinical Hospital, UMF Carol Davila, Bucharest, Romania, 4“Dr. I. Cantacuzino” Hospital, Bucharest, Romania, 5Rheumatology, Colentina Clinical Hospital, Bucuresti, Romania, 6Rheumatology, University of Medicine and Pharmacy, Cluj-Napoca, Romania

    Background/Purpose Clinical trials have proven the efficacy of biological therapy for rheumatoid arthritis (RA) worldwide. However, high costs have set boundaries to their use, especially…
  • Abstract Number: 515 • 2014 ACR/ARHP Annual Meeting

    Dosing of Intravenous Tocilizumab in a Real-World Setting—Analyses from a US RA Registry

    Dimitrios A. Pappas1, Ani John2, Jeffrey R. Curtis3, George W. Reed4,5, Chitra Karki6, Robert Magner5, Joel M. Kremer7, Ashwini Shewade2 and Jeffrey D. Greenberg6,8, 1Columbia University, New York, NY, 2Genentech, Inc, South San Francisco, CA, 3University of Alabama at Birmingham, Birmingham, AL, 4Corrona, LLC., Southborough, MA, 5University of Massachusetts Medical School, Worcester, MA, 6Corrona, LLC, Southborough, MA, 7Albany Medical College and The Center for Rheumatology, Albany, NY, 8NYU School of Medicine, New York, NY

    Background/Purpose: In the US, the recommended starting dose of intravenous tocilizumab (TCZ) in combination with DMARDs or as monotherapy is 4 mg/kg every 4 weeks…
  • Abstract Number: 2873 • 2014 ACR/ARHP Annual Meeting

    Epratuzumab Induces Broad Inhibition of B Cell Receptor Proximal Signaling but Has Opposing Effects on Distal Signaling in B Cell Subsets: A Profile of Effects on Functional Immune Signaling By Single Cell Network Profiling

    Alison Maloney1, Drew Hotson2, Stephen Rapecki1, Gianluca Fossati1, Simon Lumb1, David Rosen2, Santosh Putta2, Nikil Wale2, David Spellmeyer2, Alessandra Cesano2, Rachael Hawtin2 and Anthony Shock1, 1UCB Pharma, Slough, United Kingdom, 2Nodality Inc., South San Francisco, CA

    Background/Purpose Epratuzumab is a humanized monoclonal antibody targeting the B cell-specific protein CD22 and is in Phase 3 clinical trials in patients with systemic lupus…
  • Abstract Number: 1836 • 2014 ACR/ARHP Annual Meeting

    Safety of Zoster Vaccination Administration in Rheumatic Patients  on Current Biologic Therapy

    Stephen Lindsey1, Brandi Oufnac2 and Holly Walker2, 1Chief Div of Rheumatology, Ochsner Clinic Baton Rouge, Baton Rouge, LA, 2Rheumatology, Ochsner Health Systems, Baton Rouge, LA

    Background/Purpose Herpes Zoster (HZ) occurs in 1 in 3 people in the U.S. during their lifetime.  The greatest risk factor is age.  Immune suppression from…
  • Abstract Number: 1146 • 2014 ACR/ARHP Annual Meeting

    Cost-Effectiveness of Adalimumab for Rheumatoid Arthritis in Germany

    Christian Gissel1, Georg Götz2, Holger Repp3 and Uwe Lange4, 1Rheumatology, Justus-Liebig-University Giessen, Giessen, Germany, 2Department of Economics and Business, Justus-Liebig-University Giessen, Giessen, Germany, 3Department of Medicine, Justus-Liebig-University Giessen, Giessen, Germany, 4Internal Medicine and Rheumatology, Justus-Liebig-University Giessen, Kerckhoff-Clinic, Bad Nauheim, Germany

    Background/Purpose: In Germany, Rheumatoid Arthritis (RA) can be treated with TNF-α inhibitors after the failure of conventional disease-modifying antirheumatic drugs like Methotrexate. The clinical use…
  • Abstract Number: 505 • 2014 ACR/ARHP Annual Meeting

    A Structured Approach for Comparative Benefit-Risk Assessment of Rituximab for the Treatment of Rheumatoid Arthritis

    Ani John1, George Quartey1, Patricia B. Lehane2, Nicole Mairon3, Michael Schulte3, Ashwini Shewade1, Carol Chung1 and Dominic Borie1, 1Genentech, Inc, South San Francisco, CA, 2Roche Products Ltd, Welwyn Garden City, United Kingdom, 3F. Hoffmann-La Roche Ltd, Basel, Switzerland

    Background/Purpose: Rituximab in combination with methotrexate (MTX) is indicated for the treatment of adult patients with moderate to severe active rheumatoid arthritis (RA) who have…
  • Abstract Number: 2519 • 2014 ACR/ARHP Annual Meeting

    Are Patients with Rheumatoid Arthritis Initiating a TNF Biologic Comparable to Patients Initiating a Non TNF?

    Kaleb Michaud1,2, Kunal Gandhi3, Teresa Simon4 and Sofia Pedro1, 1National Data Bank for Rheumatic Diseases, Wichita, KS, 2Internal Medicine, University of Nebraska Medical Center, Omaha, NE, 3Bristol-Myers Squibb, Princeton, NJ, 4Bristol-Myers Squibb, Hopewell, NJ

    Background/Purpose:   Comparative research has gained attention in the field of Rheumatology. Evaluations of baseline characteristics in patients receiving similar treatments are critical in the…
  • Abstract Number: 1589 • 2014 ACR/ARHP Annual Meeting

    Risk of Opportunistic Infection and Herpes Zoster Infection in a Psoriasis/Psoriatic Arthritis Cohort

    Kevin L. Winthrop1, Lang Chen2, John Baddley2, Allison Taylor3, Benjamin Chan4, Huifeng Yun5, Sarah Siegel6 and Jeffrey R. Curtis7, 1Dept of Infectious Disease, Oregon Health & Science University, Portland, OR, 2Medicine, University of Alabama at Birmingham, Birmingham, AL, 3Clinical Immunology/Rheumatology, University of Alabama at Birmingham, Birmingham, AL, 4Oregon Health and Science University, Portland, OR, 5Epidemiology, University of Alabama at Birmingham School of Public Health, Birmingham, AL, 6Oregon Health & Science University, Portland, OR, 7The University of Alabama at Birmingham, Birmingham, AL

    Background/Purpose: Psoriasis/Psoriatic arthritis (PsO/PsA) often requires treatment with systemic agents. Some of these agents are associated with infectious adverse events. Few studies have described the…
  • Abstract Number: 1145 • 2014 ACR/ARHP Annual Meeting

    Evaluation of Biologic Treatment Patterns, Clinical Outcomes, and Healthcare Resource Utilization Post-Tumor Necrosis Factor Inhibitor Discontinuation in Rheumatoid Arthritis

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

    Background/Purpose: For rheumatoid arthritis (RA) patients (pts) with inadequate response to a TNF inhibitor (TNFi), limited evidence exists from observational studies and indirect comparisons of…
  • Abstract Number: 495 • 2014 ACR/ARHP Annual Meeting

    Discontinuation of Biologics in Patients with Rheumatoid Arthritis after Achieving Low-Activity Disease Status

    Moeko Ochiai1, Eri Sato1, Eiichi Tanaka1, Eisuke Inoue1, Ayako Nakajima1, Shigeki Momohara2, Atsuo Taniguchi2 and Hisashi Yamanaka2, 1Rheumatology, Institute of Rheumatology, Tokyo Women’s Medical University, Tokyo, Japan, 2Institute of Rheumatology, Tokyo Women’s Medical University, Tokyo, Japan

    Background/Purpose: Several clinical trials have reported bio-free remission or discontinuation of biologic DMARDs; however, these findings have not been confirmed in a real-world setting. The…
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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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