ACR Meeting Abstracts

ACR Meeting Abstracts

  • Meetings
    • ACR Convergence 2025
    • ACR Convergence 2024
    • ACR Convergence 2023
    • 2023 ACR/ARP PRSYM
    • ACR Convergence 2022
    • ACR Convergence 2021
    • 2020-2009 Meetings
    • Download Abstracts
  • Keyword Index
  • Advanced Search
  • Your Favorites
    • Favorites
    • Login
    • View and print all favorites
    • Clear all your favorites
  • ACR Meetings
  • Abstract Number: 1505 • 2014 ACR/ARHP Annual Meeting

    The Biosimilar Landscape: A Systematic Review of Its Current Status

    Niti Goel1,2 and Kamali Chance3, 1Rheumatology Center of Excellence, Quintiles, Durham, NC, 2Duke University Medical Center, Durham, NC, 3Global Biosimilars Unit, Quintiles, Durham, NC

    Background/Purpose In the last 5 years, the number of biosimilars in development for the treatment of immunologic diseases has increased as innovator etanercept (ETA), infliximab (IFX), adalimumab…
  • Abstract Number: 1504 • 2014 ACR/ARHP Annual Meeting

    Pharmacokinetic Equivalence of ABP 501 Relative to Adalimumab: Results from a Randomized, Single-Blind, Single-Dose, Parallel Group Study in Healthy Subjects

    Primal P. Kaur1, Vincent Chow2, Nan Zhang3, Mike Moxness4 and Richard Markus3, 1Amgen, Inc., Thousand Oaks, CA, 2Pharmacokinetics and Drug Metabolism, Amgen, Inc., Seattle, WA, 3Biosimilars, Amgen, Inc., Thousand Oaks, CA, 4Clinical Immunology and BSM, Amgen, Inc., Thousand Oaks, CA

    Background/Purpose Adalimumab is a recombinant IgG1 monoclonal antibody that binds to TNFα blocking its interaction with p55 and p75 cell surface receptors. ABP 501 is…
  • Abstract Number: 1503 • 2014 ACR/ARHP Annual Meeting

    Demonstration of Functional Similarity Comparing Adalimumab to Biosimilar Candidate ABP 501

    Teresa Born1, Jyoti Velayudhan2, Yuh-fung Chen3, Heather Thomas4, Christina Pastula2, Gwen Maher3 and Ryan Brown4, 1Biosimilars Process Development, Amgen, Seattle, WA, 2Functional Biocharacterization, Amgen, Seattle, WA, 3Functional Biocharacterization, Amgen, Thousand Oaks, CA, 4Inflammation Research, Amgen, Seattle, WA

    Background/Purpose: ABP 501 is being developed as a biosimilar to adalimumab, a recombinant monoclonal antibody that binds tumor necrosis factor alpha (TNF) thus inhibiting engagement…
  • Abstract Number: 1522 • 2014 ACR/ARHP Annual Meeting

    Impact of Sarilumab on Health Related Quality of Life (HRQoL),  Fatigue, and Sleep in Rheumatoid Arthritis Patients at Week 24 – Results of a Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multi-Center Study

    Vibeke Strand1, George Joseph2, Hubert van Hoogstraten2, Chieh-I Chen3, Chungpeng Fan2, Paulo Carita4, Neil Graham3, Tanya Momtahen2 and Mark C Genovese5, 1Biopharmaceutical Consultant, Portola Valley, CA, 2Sanofi, Bridgewater, NJ, 3Regeneron Pharmaceuticals, Inc., Tarrytown, NY, 4Sanofi, Chilly-Mazarin, France, 5Division of Immunology and Rheumatology, Stanford University Medical Center, Palo Alto, CA

    Background/Purpose: Sarilumab, a fully human monoclonal antibody directed against the IL-6 receptor, demonstrated efficacy in the phase 3 part of the RA-MOBILITY study (NCT01061736) in…
  • Abstract Number: 1521 • 2014 ACR/ARHP Annual Meeting

    Sustained Improvements in Magnetic Resonance Imaging Outcomes with Abatacept Following the Withdrawal of All Treatment in Patients with Early Rheumatoid Arthritis

    C Peterfy1, Gerd Burmester2, Vivian P. Bykerk3, B G Combe4, J C DiCarlo1, Daniel E. Furst5, T W J Huizinga6, C S Karyekar7, D Wong7, Philip G. Conaghan8 and P Emery9, 1Spire Sciences, Inc., Boca Raton, FL, 2Charité – University Medicine Berlin, Berlin, Germany, 3Hospital for Special Surgery, Weill Cornell Medical College, New York, NY, 4Hôpital Lapeyronie, Montpellier, France, 5University of California at Los Angeles, Los Angeles, CA, 6Leiden University Medical Center, Leiden, Netherlands, 7Bristol-Myers Squibb, Princeton, NJ, 8NIHR-Leeds Musculoskeletal Biomedical Research Unit and Leeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds, Leeds, United Kingdom, 9University of Leeds, Leeds, United Kingdom

    Background/Purpose: Biologic treatment can lead to improved clinical outcomes in early RA. In the Assessing Very Early Rheumatoid arthritis Treatment (AVERT) study, abatacept (ABA) +…
  • Abstract Number: 1520 • 2014 ACR/ARHP Annual Meeting

    Gene Expression Analyses of Abatacept- and Adalimumab-Treated Patients from the Ample Trial

    S Bandyopadhyay1, M Maldonado1, M Schiff2, ME Weinblatt3, Roy Fleischmann4 and SE Connolly1, 1Bristol-Myers Squibb, Princeton, NJ, 2University of Colorado, Denver, CO, 3Brigham and Women's Hospital, Boston, MA, 4University of Texas Southwestern Medical Center, Dallas, TX

    Background/Purpose: The distinct mechanisms of action (MoA) of abatacept (ABA) and adalimumab (ADA) are expected to manifest in different transcriptional profiles in RA patients (pts).…
  • Abstract Number: 1519 • 2014 ACR/ARHP Annual Meeting

    Implementation of an Acid Dissociation Procedure for Immunogenicity Detection in Patients Treated with ANTI-TNF Drugs

    Francisca Llinares-Tello1, Jose Rosas2, José M. Senabre-Gallego3, Gregorio Santos-Soler3, Carlos Santos-Ramirez4, Esteban Salas-Heredia3, Xavier Barber5, Juan Molina1, Catalina Cano3, Ana Pons3 and Group Aire-MB3, 1Laboratory, Hospital Marina Baixa, Villajoyosa, Spain, 2Rheumatology, Hospital Marina Baixa. Villajoyosa, Villajoyosa, Spain, 3Rheumatology, Hospital Marina Baixa, Villajoyosa, Spain, 4Rheumatology, Hospital Marina Salud, Denia, Spain, 5Universidad Miguel Hernández, CIO, Elche, Spain

    Background/Purpose To evaluate the application of an acid dissociation procedure in monitoring patients with subtherapeutic serum concentrations of infliximab (IFX), adalimumab (ADL) and etanercept (ETN),…
  • Abstract Number: 1518 • 2014 ACR/ARHP Annual Meeting

    Disentangling the Effects of Tocilizumab on Neutrophil Survival and Function

    Timo Gaber1,2,3, Martin Hahne4, Cindy Strehl2, Paula Hoff1, Yvonne Doerffel5, Eugen Feist1, Gerd Burmester1 and Frank Buttgereit6, 1Department of Rheumatology and Clinical Immunology, Charité University Medicine, Berlin, Germany, 2German Rheumatism Research Center (DRFZ), Berlin, Germany, 3Berlin-Brandenburg Center of Regenerative Therapies (BCRT), Berlin, Germany, 4Berlin-Brandenburg School of Regenerative Therapies (BSRT), Berlin, Germany, 5Department of Gastroenterology and Hepatology, Charité University Medicine, Berlin, Germany, 6Charité University Hospital, Berlin, Germany

    Background/Purpose The synovial tissue in rheumatoid arthritis (RA) represents a hypoxic environment with up-regulated pro-inflammatory cytokines and cellular infiltrates including neutrophils. Tocilizumab, a humanized IgG1…
  • Abstract Number: 1517 • 2014 ACR/ARHP Annual Meeting

    Analysis of Gene Expression Fluctuation with Abatacept Highlights the Involvement of the Proteasome Pathway As a Mechanism of Action of Abatacept in Rheumatoid Arthritis

    C Derambure1, O Vittecoq1,2, G Dzangue Tchoupou1, Maria-Antonietta d'Agostino3, P Gaudin4, C Gaillez5, M Le Bars6 and T Lequerré1,2, 1Inserm 905, Institute for Biomedical Research, University of Rouen, Rouen, France, 2Department of Rheumatology, Rouen University Hospital, Rouen, France, 3AP-HP Ambroise Paré Hospital, Boulogne-Billancourt, France, 4Department of Rheumatology, University Hospital Grenoble, Grenoble, France, 5Formerly of Bristol-Myers Squibb, Rueil-Malmaison, France, 6Bristol-Myers Squibb, Rueil-Malmaison, France

    Background/Purpose: Abatacept (ABA) is a biologic therapy targeting T cells, which play a major role in the pathophysiology of RA. Overall, 57.1% of patients reached…
  • Abstract Number: 1488 • 2014 ACR/ARHP Annual Meeting

    Clinical Efficacy of Add-on Iguratimod Therapy in Patients with Active Rheumatoid Arthritis Despite of Methotrexate ~a Multicenter Registry Study~

    Yasuhide Kanayama1, Toshihisa Kojima2, Atsushi Kaneko3, Yuji Hirano4, Nobunori Takahashi2, Shinya Hirabara4 and Naoki Ishiguro2, 1Orthopedic Surgery and Rheumatology, Toyota Kosei Hospital, Toyota, Japan, 2Orthopaedic Surgery and Rheumatology, Nagoya University Graduate School of Medicine, Nagoya, Japan, 3Orthopedic Surgery and Rheumatology, Nagoya Medical Center, Nagoya, Japan, 4Rheumatology, Toyohashi Municipal Hospital, Toyohashi, Japan

    Background/Purpose  Iguratimod (IGU) is a small-molecule antirheumatic drug that was approved in Japan in September 2012. IGU suppressed tumor necrosis factor-alpha-induced production of interleukin (IL)-6,…
  • Abstract Number: 1486 • 2014 ACR/ARHP Annual Meeting

    Rapid Onset of Clinical Benefit Is Associated with a Reduction in Validated Biomarkers of Disease in Patients with Rheumatoid Arthritis Treated with Mavrilimumab, a Human Monoclonal Antibody Targeting GM-CSFRá

    Iain B. McInnes1, Gerd Burmester2, Joel M. Kremer3, Pedro Miranda4, Mariusz Korkosz5, Jiri Vencovsky6, Andrea Rubbert-Roth7, Eduardo Mysler8, David Close9, Matthew A. Sleeman10, Alex Godwood11, Sara Sandbach12, Patricia C. Ryan13, Dominic Sinibaldi14, Wendy White13, Nadine A. Defranoux15 and Michael Weinblatt16, 1Institute of Infection, Immunity and Inflammation, University of Glasgow, Glasgow, United Kingdom, 2Department of Rheumatology and Clinical Immunology, Charité - University Medicine Berlin, Berlin, Germany, 3Medicine, Albany Medical College and the Center for Rheumatology, Albany, NY, 4Centro de Estudios Reumatologicos, Santiago, Chile, 5Inernal Medicine and Gerontology, Malopolskie Centrum Medyczne, Krakow, Poland, 6Rheumatology, Charles University Institute of Rheumatology, Prague, Czech Republic, 7Med Clinic I, University of Cologne, koln, Germany, 8Rheumatology, OMI, Buenos Aires, Argentina, 9Clinical Development, MedImmune Ltd, Cambridge, United Kingdom, 10Respiratory, Inflammation and Autoimmunity, MedImmune Ltd, Cambridge, United Kingdom, 11Clinical Biostatics and Data Management, MedImmune Ltd, Cambridge, United Kingdom, 12Clinical biologics, MedImmune Ltd, Cambridge, United Kingdom, 13Translational Sciences, MedImmune, Gaithersburg, MD, 14R&D IS Translational & Clinical Informatics, MedImmune, Gaithersburg, MD, 15Crescendo Bioscience Inc., South San Francisco, CA, 16Rheumatology, Brigham & Women's Hospital, Harvard Medical School, Boston, MA

    Background/Purpose Macrophages are pivotal to rheumatoid pathogenesis and their inflammatory products drive many of the signs and symptoms of disease. Mavrilimumab inhibits macrophage activation and…
  • Abstract Number: 1485 • 2014 ACR/ARHP Annual Meeting

    Analysis of Patient-Reported Outcomes during Treatment with Mavrilimumab, a Human Monoclonal Antibody Targeting GM-CSFRá, in the Randomized Phase 2b Earth Explorer 1 Study

    Joel M. Kremer1, Gerd Burmester2, Michael Weinblatt3, Angela Williams4, Niklas Karlsson5, Alex Godwood6 and David Close7, 1Medicine, Albany Medical College and the Center for Rheumatology, Albany, NY, 2Department of Rheumatology and Clinical Immunology, Charité University Medicine, Berlin, Germany, 3Rheumatology, Brigham & Women's Hospital, Harvard Medical School, Boston, MA, 4MedImmune Ltd, Cambridge, United Kingdom, 5Health Economics and Outcomes Research, AstraZeneca, Molndal, Sweden, 6Clinical Biostatics and Data Management, MedImmune Ltd, Cambridge, United Kingdom, 7Clinical Development, MedImmune Ltd, Cambridge, United Kingdom

    Background/Purpose Active RA significantly impairs health-related quality of life (HRQoL) and physical function of patients. Granulocyte-macrophage colony-stimulating factor (GM-CSF) plays a key role in macrophage…
  • Abstract Number: 1484 • 2014 ACR/ARHP Annual Meeting

    Discovery of ARN-4079 – a Potent, Orally Available Dual Target Inhibitor of Janus Kinase 3 (JAK3) and Interleukin-2 Inducible T-Cell Kinase (ITK) for Rheumatoid Arthritis

    Hariprasad Vankayalapati1, Venkatakrishnareddy Yerramreddy1, Philip Bendele2, Alison Bendele3, Rueban Jacob Anicattu Issac4, Ram Sudheer Adluri5, Philip LoGrasso6 and Joel M. Kremer7, 1Early Discovery and Medicinal Chemistry, Arrien Pharmaceuticals, Salt Lake City, UT, 2Principal Investigator CIA models, Bolder BioPATH, Inc., Boulder, CO, 3Pathologist, Bolder BioPATH Inc., Boulder, CO, 4Biology, GVK Biosciences Private Limited., Hyderabad, India, 5GVK Biosciences Private Limited., Hyderabad, India, 6Molecular Therapeutics, The Scripps Research Institute, Jupiter, FL, 7Medicine, Albany Medical College and the Center for Rheumatology, Albany, NY

    Background/Purpose: The Non-receptor tyrosine kinases, JAK3 and ITK are key regulators of cytokine pathways and are important clinically validated targets, which offer the potential for…
  • Abstract Number: 1483 • 2014 ACR/ARHP Annual Meeting

    Efficacy and Safety of Baricitinib in Japanese Rheumatoid Arthritis Patients during a 52 Week Extension Phase

    Yoshiya Tanaka1, Kahaku Emoto2, Zhihong Cai2, Douglas E. Schlichting3, Terence Rooney3 and William Macias3, 1University of Occupational and Environmental Health, Japan, Kitakyushu, Japan, 2Eli Lilly Japan K.K., Kobe, Japan, 3Eli Lilly and Company, Indianapolis, IN

    Background/Purpose Baricitinib (bari), an oral JAK1/JAK2 signaling inhibitor, was evaluated in a blinded phase 2b study for 12 weeks as a treatment for rheumatoid arthritis…
  • Abstract Number: 1502 • 2014 ACR/ARHP Annual Meeting

    A Phase I Trial Comparing PF-05280586 (A Potential Biosimilar) and Rituximab in Subjects with Active Rheumatoid Arthritis

    Jean-Claude P. Becker1, Donghua Yin2, Lisa Ann Melia3, Ruifeng Li4, Barry Gumbiner5, Dolca Thomas6, George Spencer-Green7 and Xu Meng2, 1Pfizer Biosimilars Research and Development/Medical Affairs., Pfizer Inc., New York, NY, 2Clinical Pharmacology/Pharmacometrics, Pfizer Inc., San Diego, CA, 3Biotechnology Clinical Development, Pfizer Inc., San Diego, CA, 4Biostatistics, Pfizer Inc., Cambridge, MA, 5Worldwide Research and Development, Pfizer Inc., San Diego, CA, 6Biosimilars Research and Development Unit, Pfizer Inc., New York, NY, 7Worldwide Research and Development, Pfizer Inc., Cambridge, MA

    Background/Purpose: PF-05280586, a proposed biosimilar to rituximab, has the same primary amino acid sequence as rituximab with similar physicochemical and in vitro functional properties. This…
  • « Previous Page
  • 1
  • …
  • 2131
  • 2132
  • 2133
  • 2134
  • 2135
  • …
  • 2607
  • Next Page »
Advanced Search

Your Favorites

You can save and print a list of your favorite abstracts during your browser session by clicking the “Favorite” button at the bottom of any abstract. View your favorites »

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].

Wiley

  • Online Journal
  • Privacy Policy
  • Permissions Policies
  • Cookie Preferences

© Copyright 2025 American College of Rheumatology