ACR Meeting Abstracts

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Abstracts tagged "Biologics"

  • Abstract Number: 2449 • 2017 ACR/ARHP Annual Meeting

    Comparative Effectiveness of Tocilizumab (TCZ) Monotherapy with Tumor Necrosis Factor Inhibitors (TNFi) in Combination with Varying Doses of Methotrexate (MTX) in Patients with Rheumatoid Arthritis

    Leslie R Harrold1, George W. Reed1, Jennie Best2, Steve Zlotnick2, Gioia Persuitte3 and Joel Kremer4, 1University of Massachusetts Medical School, Worcester, MA, 2Genentech, Inc., South San Francisco, CA, 3Corrona, LLC, Southborough, MA, 4Albany Medical College and The Center for Rheumatology, Albany, NY

    Background/Purpose: Clinical studies have shown that the efficacy of TCZ monotherapy (TCZ mono) is superior to that of TNFi monotherapy and comparable to that of…
  • Abstract Number: 2871 • 2017 ACR/ARHP Annual Meeting

    Anti-RA33 (hnRNP-A2/B1) Autoantibodies Are Associated with the Therapeutic Response to Methotrexate and Anti-TNF Treatment in Patients with Rheumatoid Arthritis

    Daniela Sieghart1, Paul Studenic1, Farideh Alasti2, Daniel Aletaha3, Josef S. Smolen1 and Günter Steiner2, 1Medical University Vienna, Division of Rheumatology, Department of Internal Medicine III, Vienna, Austria, 2Rheumatology, Medical University of Vienna, Vienna, Austria, 3Department of Medicine III, Division of Rheumatology, Medical University of Vienna, Vienna, Austria

    Background/Purpose: Besides the determination of rheumatoid factor (RF) and anti-citrullinated protein antibodies (ACPA), anti-RA33 antibodies (which are directed to the nuclear antigen hnRNP-A2/B1) could be…
  • Abstract Number: 595 • 2017 ACR/ARHP Annual Meeting

    Improved Patient-Reported Outcomes in Psoriatic Arthritis Patients Treated with Abatacept: Results from a Phase III Trial

    Vibeke Strand1, E Alemao2, T Lehman2, A Johnsen2, S Banerjee2, HA Ahmad2 and Philip J Mease3, 1Stanford University, Palo Alto, CA, 2Bristol-Myers Squibb, Princeton, NJ, 3Swedish Medical Center and University of Washington, Seattle, WA

    Background/Purpose: In the Phase III ASTRAEA study (NCT01860976), abatacept (ABA) significantly increased ACR20 responses, alleviating musculoskeletal symptoms in patients (pts) with active psoriatic arthritis (PsA).1…
  • Abstract Number: 1041 • 2017 ACR/ARHP Annual Meeting

    Real-World Utilization of Biosimilars for Management of Rheumatoid Arthritis (RA) in the US

    Janna Radtchenko, Yolaine Smith, Jonathan Kish and Bruce Feinberg, Specialty Solutions, Cardinal Health, Dallas, TX

    Background/Purpose: A biosimilar product is a biological product highly similar to another FDA-approved biological product, reference product, and has no clinically meaningful differences in safety…
  • Abstract Number: 1525 • 2017 ACR/ARHP Annual Meeting

    Characteristics and Treatment Patterns Among Patients with Psoriatic Arthritis Initiating Subcutaneously Administered Biologics: Descriptive Analyses from a US Claims Database

    Kurt R. Oelke1, Rahul Garg2, Peter Hur3, Olivier Chambenoit3, Amar Q. Majjhoo4, Stephani Gray5, Kate Higgins5 and Jacqueline B. Palmer3, 1Rheumatic Disease Center, Glendale, WI, 2PRO Unlimited, Inc, East Hanover, NJ, 3Novartis Pharmaceuticals Corporation, East Hanover, NJ, 4Shores Rheumatology, St. Clair Shores, MI, 5Truven Health Analytics, Cambridge, MA

    Background/Purpose: To better understand the real-world efficacy of biologics for the treatment of psoriatic arthritis (PsA), there is a need to evaluate the persistence and…
  • Abstract Number: 2460 • 2017 ACR/ARHP Annual Meeting

    Patient-Reported Outcomes Following Discontinuation of Methotrexate in Patients with Rheumatoid Arthritis Treated with Subcutaneous Tocilizumab: Results from a Randomized Controlled Trial

    Joel Kremer1, William F C Rigby2, Nora Singer3, Christine Birchwood4, Darcy Gill4, William Reiss4, Jennie Best4, Jinglan Pei4 and Margaret Michalska4, 1Albany Medical College, Albany, NY, 2Geisel School of Medicine at Dartmouth, Lebanon, NH, 3Case Western Reserve University School of Medicine, Cleveland, OH, 4Genentech, Inc., South San Francisco, CA

    Background/Purpose: Patients with rheumatoid arthritis (RA) often receive methotrexate (MTX) in combination with biologics; however, MTX may be discontinued due to intolerance or to reduce…
  • Abstract Number: 2878 • 2017 ACR/ARHP Annual Meeting

    Efficacy and Safety Results of Guselkumab in Patients with Active Psoriatic Arthritis over 56 Weeks from a Phase 2a, Randomized, Double-Blind, Placebo-Controlled Study

    Atul A. Deodhar1, Alice B Gottlieb2, Wolf-Henning Boehncke3, Bin Dong4, Yuhua Wang4, Yanli Zhuang4, William Barchuk5, Xie L. Xu5 and Elizabeth Hsia4, 1Division of Arthritis & Rheumatic Diseases OP09, Oregon Health & Science University, Portland, OR, 2Department of Dermatology, New York Medical College, Valhalla, NY, 3Geneva University Hospital and University of Geneva, Geneva, Switzerland, 4Janssen Research & Development, LLC, Spring House, PA, 5Janssen Research & Development, LLC, San Diego, CA

    Background/Purpose: Evaluate efficacy and safety of guselkumab (GUS) in patients (pts) with active psoriatic arthritis (PsA) over 56 weeks (wks). Methods: Pts w/active PsA (defined…
  • Abstract Number: 597 • 2017 ACR/ARHP Annual Meeting

    Ixekizumab Improves Patient-Reported Outcomes through 52 Weeks in Patients with Active Psoriatic Arthritis and Previous Inadequate Response to Tumor Necrosis Factor-Inhibitors

    Arthur Kavanaugh1, Helena Marzo-Ortega2, Ronald Vender3, Julie Birt4, David Adams4, Olivier Benichou4, Chen-Yen Lin4 and Peter Nash5, 1Medicine, University of California, San Diego, La Jolla, CA, 2Department of Rheumatology, Chapel Allerton Hospital, Leeds, United Kingdom, 3Dermatrials Research, Inc., Hamilton, ON, Canada, 4Eli Lilly and Company, Indianapolis, IN, 5University of Queensland, Brisbane, Australia

    Background/Purpose: Ixekizumab (IXE) is a high affinity monoclonal antibody that selectively targets interleukin-17A. Up to 24 weeks, IXE was superior to placebo (PBO) in improving…
  • Abstract Number: 1044 • 2017 ACR/ARHP Annual Meeting

    Medical Care Costs Associated with Rheumatoid Arthritis in the US: A Meta-Analysis

    Andrew Hresko1, Tzu-Chieh Lin2 and Daniel H. Solomon3, 1Tufts Medical School, Boston, MA, 2Health Outcomes, Amgen, Thousand Oaks, CA, 3Brigham and Women's Hospital and Harvard Medical School, Boston, MA

    Background/Purpose:   Rheumatoid arthritis (RA) is a morbid, mortal, and costly condition without a cure. Treatments for RA have expanded over the last two decades…
  • Abstract Number: 1528 • 2017 ACR/ARHP Annual Meeting

    Secukinumab Provides Rapid and Sustained Pain Relief in Ankylosing Spondylitis Patients with Normal or Elevated Baseline CRP Levels and Correlated with Improvement in Fatigue

    Atul A. Deodhar1, Philip G. Conaghan2, Tore K Kvien3, Vibeke Strand4, Lawrence Rasouliyan5, Brian Porter6, Steffen Jugl7 and Kunal Gandhi6, 1Oregon Health & Science University, Portland, OR, 2University of Leeds, Leeds, United Kingdom, 3Diakonhjemmet Hospital, Oslo, Norway, 4Stanford University School of Medicine, Palo Alto, CA, 5RTI Health Solutions, Barcelona, Spain, 6Novartis Pharmaceuticals Corporation, East Hanover, NJ, 7Novartis Pharma AG, Basel, Switzerland

    Background/Purpose: Secukinumab has demonstrated sustained efficacy in patients (pts) with active AS.1,2 We investigated improvement in pain and fatigue scores from baseline (BL) through Week…
  • Abstract Number: 2461 • 2017 ACR/ARHP Annual Meeting

    Rituximab Is Effective in the Treatment of Rheumatoid Arthritis Irrespective of Body Mass Index; Up to 48 Weeks Results from Phase 3 Study

    Dae-Hyun Yoo1, Won Park2, Chang-Hee Suh3, Seung-Cheol Shim4, Sang-Joon Lee5, Yun Ju Bae5, Chan Park5 and Noo Ri Han5, 1Department of Rheumatology, Hanyang University Hospital for Rheumatic Diseases, Seoul, Korea, Republic of (South), 2Medicine/Rheumatology, Inha University Hospital, Incheon, Korea, Republic of (South), 3Ajou University School of Medicine, Suwon, Korea, Republic of (South), 4Department of Internal Medicine, Chungnam National University Hospital, Daejeon, Korea, Republic of (South), 5CELLTRION, Inc., Incheon, Korea, Republic of (South)

    Background/Purpose: High body mass index (BMI) is known to be associated with inadequate clinical response to anti-TNF agents in RA patients.1 However, there are limited…
  • Abstract Number: 2879 • 2017 ACR/ARHP Annual Meeting

    Switching from Adalimumab to Chs-1420: A Randomized, Double-Blind Global Clinical Trial in Patients with Psoriasis and Psoriatic Arthritis

    Jennifer Hodge, Hong Tang, Paula O'Connor and Barbara Finck, Coherus BioSciences, Inc., Redwood City, CA

    Background/Purpose: CHS-1420 is a proposed biosimilar to adalimumab. A phase 3, randomized, double-blind, multicenter study evaluated the equivalence of CHS-1420 to adalimumab in patients with…
  • Abstract Number: 605 • 2017 ACR/ARHP Annual Meeting

    Ixekizumab Exhibits a Favorable Safety Profile during 24 Weeks of Treatment in Subjects with Active Psoriatic Arthritis: Integrated Safety Analysis of Two Randomized, Placebo Controlled, Phase III Clinical Trials

    Philip J Mease1, Gerd R. Burmester2, Susan Moriarty3, Olivier Benichou3, Wen Xu3 and Peter Nash4, 1Swedish Medical Center and University of Washington, Seattle, WA, 2Department of Rheumatology and Clinical Immunology, Charité - University Medicine Berlin, Free University and Humboldt University Berlin, Berlin, Germany, 3Eli Lilly and Company, Indianapolis, IN, 4University of Queensland, Brisbane, Australia

    Background/Purpose: Ixekizumab (IXE) is a high affinity monoclonal antibody that selectively targets IL-17A. The objective of this analysis is to report the integrated safety of…
  • Abstract Number: 1092 • 2017 ACR/ARHP Annual Meeting

    The Ottawa Biologics Safety and Screening Tool

    Chrisanna Dobrowolski1, Ines Midzic2, Denise Boone2, Anne McCarthy3, Doug Smith2, John Thomson2, Sheryl Izzi4 and Susan Humphrey-Murto2, 1Internal Medicine, The Ottawa Hospital - University of Ottawa, Ottawa, ON, Canada, 2Division of Rheumatology, Department of Medicine, The Ottawa Hospital - University of Ottawa, Ottawa, ON, Canada, 3Division of Infectious Diseases, Department of Medicine, The Ottawa Hospital - University of Ottawa, Ottawa, ON, Canada, 4Division of Endocrinology, Department of Medicine, The Ottawa Hospital - University of Ottawa, Ottawa, ON, Canada

    Background/Purpose : A large proportion of patients with rheumatologic diseases are now being treated with biologic therapies. Estimates of the use of biologics in patients…
  • Abstract Number: 1529 • 2017 ACR/ARHP Annual Meeting

    Secukinumab Demonstrates Consistent Safety over Long-Term Exposure (up to 3 years) in Patients with Active Ankylosing Spondylitis: Pooled Analysis of Three Phase 3 Trials

    Atul A. Deodhar1, Xenofon Baraliakos2, Helena Marzo-Ortega3, Joachim Sieper4, Mats Andersson5, Brian Porter6 and Todd Fox5, 1Oregon Health & Science University, Portland, OR, 2Rheumazentrum Ruhrgebiet Herne, Ruhr-University Bochum, Herne, Germany, 3NIHR LBRC, LTHT and LIRMM, UoL, Leeds, United Kingdom, 4Charité University Medicine Berlin, Berlin, Germany, 5Novartis Pharma AG, Basel, Switzerland, 6Novartis Pharmaceuticals Corporation, East Hanover, NJ

    Background/Purpose: Secukinumab has demonstrated a consistent and reliable safety profile in three Phase 3 studies in ankylosing spondylitis (AS): MEASURE 1 (NCT01358175), MEASURE 2 (NCT01649375),…
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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.).

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].

ACR Abstract Embargo Policy

Accepted abstracts are made available to the public online in advance of the meeting and are published in a special online supplement of Arthritis & Rheumatology. Information contained in those abstracts may not be released until the abstracts appear online. 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 a scientific presentation or presentation of additional new information that will be available at the time of the meeting) is under embargo until Saturday, November 11, 2023.

Violation of this policy may result in the abstract being withdrawn from the meeting and other measures deemed appropriate. Authors are responsible for notifying financial and other sponsors about this policy. If you have questions about the abstract embargo policy, please contact the public relations department at [email protected].

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