ACR Meeting Abstracts

ACR Meeting Abstracts

  • Meetings
    • ACR Convergence 2024
    • ACR Convergence 2023
    • 2023 ACR/ARP PRSYM
    • ACR Convergence 2022
    • ACR Convergence 2021
    • ACR Convergence 2020
    • 2020 ACR/ARP PRSYM
    • 2019 ACR/ARP Annual Meeting
    • 2018-2009 Meetings
    • Download Abstracts
  • Keyword Index
  • Advanced Search
  • Your Favorites
    • Favorites
    • Login
    • View and print all favorites
    • Clear all your favorites
  • ACR Meetings

Abstracts tagged "American College of Rheumatology Criteria"

  • Abstract Number: 0392 • ACR Convergence 2023

    Novel Diagnostic Markers for Rheumatoid Arthritis Including Anti-CarP (Carbamylated Protein), Anti-Sa (Citrullinated Vimentin) and Anti-CEP1 (Citrullinated Enolase Peptide1) Are Frequently Positive in Diagnostic Profiles

    Jane Yang1, Rubio Punzalan1, Lehrhoff Andrew1, Michael Nappi1, Vincent ricchiuti2, Michael Zikry1 and Kelly Chun1, 1Labcorp, Calabasas, CA, 2Labcorp, Dublin, OH

    Background/Purpose: Despite the diagnostic contribution of Anti-CCP3.1 (cyclic citrillunated peptide) antibody and RF (rheumatoid factor) as classified by the 2010 ACR/EULAR RA criteria, approximately one-third…
  • Abstract Number: 1131 • ACR Convergence 2023

    Clinical Phenotypes of IgG4-related Disease in a Multi-ethnic Singapore Cohort

    Choon Guan Chua1, Weida Chew1, Jeggrey Kay Wee Kam1, Hwee-Pin Phua1, Chengzi Chow1, Carol Yee-Leng Ng1, Wei-Yen Lim1, Ru Sin Lim1, Jereme Yijin Gan1, Mung-Ee Loh1, Tianrong Yeo2, David Zhiwei Law1, Stephrene Seok Wei Chan3, Amanda Francesca Ya-Fang Cheang4, Yong-Howe Ho1 and Charles Kien-Fong Vu1, 1Tan Tock Seng Hospital, Singapore, Singapore, 2National Neurology Institute, Singapore, Singapore, 3National University Hospital, Singapore, Singapore, 4Woodlands Health Campus, Singapore, Singapore

    Background/Purpose: IgG4-related disease (IgG4-RD) is an immune-mediated condition that is heterogenous and can result in organ failure. To understand the disease profile of our local…
  • Abstract Number: L02 • ACR Convergence 2022

    Bimekizumab Treatment in Biologic DMARD-Naïve Patients with Active Psoriatic Arthritis: 52-Week Efficacy and Safety Results from a Phase 3, Randomized, Placebo-Controlled, Active Reference Study

    Christopher Ritchlin1, Laura Coates2, Iain McInnes3, Philip J. Mease4, Joseph Merola5, Yoshiya Tanaka6, Akihiko Asahina7, Laure Gossec8, Alice Gottlieb9, Diamant Thaci10, Barbara Ink11, Deepak Assudani11, Rajan Bajracharya11, Vish Shende11, Jason Coarse12 and Robert Landewé13, 1University of Rochester Medical Center, Rochester, NY, 2Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Diseases, University of Oxford and Oxford Biomedical Research Centre, Oxford University Hospitals NHS Trust, Oxford, United Kingdom, 3College of Medical Veterinary and Life Sciences, University of Glasgow, Glasgow, United Kingdom, 4Swedish Medical Center/Providence St. Joseph Health and University of Washington School of Medicine, Seattle, WA, 5Harvard Medical School, Brigham and Women’s Hospital, Boston, MA, 6University of Occupational and Environmental Health Japan, Kitakyushu, Japan, 7Department of Dermatology, The Jikei University School of Medicine, Tokyo, Japan, 8Sorbonne Universités, UPMC Univ Paris 06, GRC-UPMC 08 (EEMOIS); AP-HP, Hôpital Pitié Salpêtrière, Rheumatology Department, Paris, France, Paris, France, 9Department of Dermatology, Icahn School of Medicine at Mount Sinai, New York, NY, 10Institute and Comprehensive Center for Inflammation Medicine, University of Lübeck, Lübeck, Germany, 11UCB Pharma, Slough, United Kingdom, 12UCB Pharma, Raleigh, NC, 13Amsterdam Rheumatology & Clinical Immunology Center, Amsterdam, and Zuyderland MC, Heerlen, Netherlands

    Background/Purpose: Bimekizumab (BKZ) is a monoclonal IgG1 antibody that selectively inhibits IL-17F in addition to IL-17A. BKZ treatment has demonstrated superior efficacy in joints and…
  • Abstract Number: 0455 • ACR Convergence 2022

    Performance of 2022 American College of Rheumatology/European Alliance of Associations for Rheumatology Classification Criteria in Turkish Vasculitis Patients

    Ummugulsum Gazel1, Sevinc Can Sandikci2, Ahmet Omma3, Sinem Burcu Kocaer4, Fatoş Onen5, Onay Gercik6, Servet Akar7, Kerem Abacar8, Ebru Asicioglu9, Serhan Tuglular9, Fatma Alibaz-Oner8 and Haner Direskeneli10, 1University of Ottawa, Rheumatology, Ottawa, Canada, Ottawa, ON, Canada, 2Ankara Numune Education and Research Hospital, Rheumatology, Ankara, Turkey, 3Ankara Numune Education and Research Hospital, Rheumatology, Ankara, Turkey, Istanbul, Turkey, 4Dokuz Eylul University, Faculty of Medicine, Rheumatology, Izmir, Turkey, 5Dokuz Eylul University, Faculty of Medicine, Rheumatology, İzmir, Turkey, 6Izmir Tepecik Research Hospital, Izmir, Turkey, 7Izmir Katip Celebi University School of Medicine, Izmir, Turkey, 8Marmara University, Rheumatology, Istanbul, Turkey, 9Marmara University, Faculty of Medicine, Nephrology, Istanbul, Turkey, 10Marmara University, Rheumatology, Istanbul, Istanbul, Turkey

    Background/Purpose: The American College of Rheumatology (ACR)-1990 criteria is the most used method for the classification of ANCA Associated Vasculitis (AAV). However, with ACR-1990 criteria,…
  • Abstract Number: 0917 • ACR Convergence 2022

    Fifty-two-week Results from a Phase 3, Randomized, Double-blind, Active-controlled Clinical Trial to Compare BAT1806/BIIB800, a Proposed Tocilizumab Biosimilar, with a Tocilizumab Reference Product in Subjects with Moderate to Severe RA with an Inadequate Response to Methotrexate

    Xiaomei Leng1, Piotr Leszczynski2, Sławomir Jeka3, Shengyun Liu4, Huaxiang Liu5, Malgorzata Miakisz6, Jieruo Gu7, Lali Kilasonia8, Mykola Stanislavchuk9, Xiaolei Yang10, Yinbo Zhou11, Qingfeng Dong11, Marian Mitroiu12, Janet Addison13 and Xiaofeng Zeng14, 1Peking Union Medical College Hospital, Department of Rheumatology and Clinical Immunology, Beijing, China, 2Poznan University of Medical Sciences, Department of Rheumatology, Rehabilitation and Internal Medicine, Poznan, Poland, 3University Hospital No 2 in Bydgoszcz Collegium Medicum UMK, Clinic and Department of Rheumatology and Connective Tissue Diseases, Bydgoszcz, Poland, 4First Affiliated Hospital of Zhengzhou University, Department of Rheumatology and Immunology, Zhengzhou, China, 5Qilu Hospital of Shandong University, Department of Rheumatology, Jinan, China, 6Twoja Przychodnia Centrum Medyczne, Internal Medicine and Rheumatology, Nowa Sól, Poland, 7The Third Affiliated Hospital of Sun Yat-sen University, Department of Rheumatology, Guangzhou, China, 8Tbilisi Heart and Vascular Clinic Ltd, Rheumatology, Tbilisi, Georgia, 9National Pirogov Memorial Medical University, Internal Medicine, Vinnytsia, Ukraine, 10Bio-Thera Solutions, Ltd., Research and Development, Guangzhou, China, 11Bio-Thera Solutions Ltd, Research and Development, Guangzhou, China, 12Biogen International GmbH, Evidence Generation Biosimilars, Baar, Switzerland, 13Biogen Idec Ltd, Maidenhead, United Kingdom, 14Department of Rheumatology, Peking Union Medical College Hospital (PUMCH), Chinese Academy of Medical Sciences National Clinical Research Center for Dermatologic and Immunologic Diseases (NCRC-DID), Beijing, China

    Background/Purpose: BAT1806 (also referred to as BIIB800) is a proposed biosimilar to tocilizumab reference product (TCZ). Results of this Phase 3, randomized, double-blind, active-controlled trial…
  • Abstract Number: 1599 • ACR Convergence 2022

    Bimekizumab Treatment in Patients with Active Psoriatic Arthritis and Inadequate Response to Tumor Necrosis Factor Inhibitors: 16-Week Efficacy and Safety from a Phase 3, Randomized, Double-Blind, Placebo-Controlled Study

    Joseph Merola1, Robert Landewé2, Iain B McInnes3, Philip J Mease4, Christopher Ritchlin5, Yoshiya Tanaka6, Akihiko Asahina7, Frank Behrens8, Dafna Gladman9, Laure Gossec10, Richard Warren11, Barbara Ink12, Deepak Assudani12, Rajan Bajracharya12, Jason Coarse13 and Laura Coates14, 1Harvard Medical School, Brigham and Women's Hospital, Boston, MA, 2Amsterdam University Medical Center, Meerssen, Netherlands, 3Institute of Infection, Immunity and Inflammation, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, Scotland, United Kingdom, 4Swedish Medical Center/Providence St. Joseph Health, Seattle, WA, 5Allergy, Immunology and Rheumatology Division, University of Rochester Medical School, Canandaigua, NY, 6University of Occupational and Environmental Health, Kitakyusyu Fukuoka, Japan, 7Department of Dermatology, The Jikei University School of Medicine, Tokyo, Japan, 8Rheumatology University Hospital & Fraunhofer Institute Translational Medicine and Pharmacology, Goethe-University Frankfurt, Frankfurt Am Main, Germany, 9Toronto Western Hospital, Schroeder Arthritis Institute, Toronto, ON, Canada, 10Sorbonne Université, Paris, France, 11The University of Manchester, Manchester, United Kingdom, 12UCB Pharma, Slough, United Kingdom, 13UCB Pharma, Raleigh, NC, USA, Raleigh, NC, 14Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Oxford, UK, Oxford, England, United Kingdom

    Background/Purpose: Bimekizumab (BKZ) is a monoclonal IgG1 antibody that selectively inhibits IL-17F in addition to IL-17A. The phase 3 BE COMPLETE study assessed the efficacy…
  • Abstract Number: 1811 • ACR Convergence 2022

    Urate Lowering Therapy Initiation in Hospitalized Patients with Acute Gout Flares

    Emily Fan1 and Megan Krause2, 1University of Kansas School of Medicine, Kansas City, KS, 2University of Kansas, Kansas City, KS

    Background/Purpose: Identifying patients with gout who would benefit from urate lowering therapies (ULT) is of utmost importance to help limit both pain and functional pain.…
  • Abstract Number: 1822 • ACR Convergence 2022

    A Double-Blind, Placebo-Controlled, Ascending Dose Phase 2a Study of ABP-671, a Novel, Potent and Selective URAT1 Inhibitor, in Patients with Gout or Hyperuricemia

    Marc Gurwith1, Deon Smith2, Paul Bird3, Jessica Leung4, Mark Bloch5, Joshua Kim6, Rahul Mohan7, Anthony Houston8, Oscar Cumming9, Ann Madrid10, Ullrich Schwertschlag11, Jerry Liu12, Roy Wu13, Jason Xu14, Adam Jin14 and William Dongfang Shi15, 1Jiangsu Atom Bioscience and Pharmaceutical Co., Ltd., Los Altos Hills, CA, 2Emeritus Research, Melbourne, Australia, 3Emeritus Research Sydney, Sydney, Australia, 4Austin Health, Preston, Victoria, Australia, 5Holdsworth House Medical Practice, Darlinghurst, Australia, 6Paratus Clinical Pty Ltd., New South Wales, Australia, 7Paratus Clinical Pty Ltd, Western Sydney, Australia, 8Peninsula Private Hospital, Kippa-Ring, Australia, 9Novatrials, Kotara, Australia, 10Novotech Australia, Sydney, Australia, 11Jiangsu Atom Bioscience and Pharmaceutical Co., Ltd., Palo Alto, 12Jiangsu Atom Bioscience and Pharmaceutical Co., Ltd., San Diego, 13Jiangsu Atom Bioscience and Pharmaceutical Co., Ltd., San Francisco, 14Jiangsu Atom Bioscience and Pharmaceutical Co., Ltd., Suzhou, China, 15Jiangsu Atom Bioscience and Pharmaceutical Co., Ltd., Fremont

    Background/Purpose: ABP-671, a novel selective and potent URAT1 inhibitor reduces reabsorption of uric acid (UA) at the renal proximal tubule, and significantly decreases serum uric…
  • Abstract Number: 2046 • ACR Convergence 2022

    Agreement Between Labial Biopsy and the OMERACT Grey-scale Ultrasound Scoring System for Salivary Glands in a Single-center Cohort of Patients with Suspected Sjögren’s Syndrome

    Viktoria Fana1, Nanna Surlemont Schmidt2, Uffe Møller Døhn1, Simon Krabbe3 and Lene Terslev4, 1Center for Rheumatology and Spine Diseases, Rigshospitalet, Copenhagen, Denmark, 2Rigshospitalet, Copenhagen, Denmark, 3Rigshospitalet, København, Denmark, 4Copenhagen University Hospital Glostrup, Glostrup, Denmark

    Background/Purpose: Ultrasound is a promising non-invasive tool in the evaluation of the salivary glands for parenchymal changes related to Sjögrens Syndrome (SS). The OMERACT Ultrasound…
  • Abstract Number: 2113 • ACR Convergence 2022

    Improvement in Key PsA Core Domains with Guselkumab Treatment in an Enriched Population of ACR20 Non-Responders at Week 24: Post Hoc Analysis of Two Phase 3 Studies

    Dennis McGonagle1, Derek Haaland2, Philip Helliwell3, A. Marilise Marrache4, May Shawi5, Emmanouil Rampakakis6, Peter Nash7, Fedra Irazoque Palazuelos8 and Arthur Kavanaugh9, 1Leeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds; National Institute for Health Research, Leeds Biomedical Research Centre, Leeds Teaching Hospitals NHS Trust, Leeds, United Kingdom, 2The Waterside Clinic, Oro Medonte, ON, Canada, 3Leeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds, Leeds, United Kingdom, 4Janssen Inc., Dollard-des-Ormeaux, QC, Canada, 5Immunology Global Medical Affairs, Janssen Pharmaceutical Companies of Johnson & Johnson, Horsham, PA, 6McGill University, Department of Pediatrics and JSS Medical Research, Montréal, QC, Canada, 7School of Medicine, Griffith University, Sunshine Coast, Australia, 8Angeles Mocel Hospital; Universidad Autónoma de México, Ciudad de México, Mexico, 9University of California San Diego, La Jolla, CA

    Background/Purpose: Despite available PsA treatments, a portion of PsA patients (pts) does not achieve improvements in PsA signs and symptoms according to ACR response criteria.…
  • Abstract Number: 1654 • ACR Convergence 2021

    Comparative Characteristics of the Natural Course of Early Rheumatoid Arthritis with Onset at a Young Age (18-49 Years) and Older (50 Years and Older) Patients Who Did Not Take DMARDs, Biologics, Other Targeted Drugs, Corticoids According to the Russian Register of Arthritis OREL

    Azamat Satybaldyev, Galina Gridneva, Anna Misiyuk, Natalia Demidova, Kamalia Kasumova and Evgeny Nasonov, V.A. Nasonova Reseach Institute of Rheumatology, Moscow, Russia

    Background/Purpose: Comparison of frequency of different clinical features of the natural course at the stage of early rheumatoid arthritis (RA) in patients with young and…
  • Abstract Number: 1733 • ACR Convergence 2021

    Classification of Patients with Systemic Lupus Erythematosus Enrolled in 2 Phase 3 Trials by EULAR/ACR 2019 Criteria

    Martin Aringer1, Ian N. Bruce2, Richard Furie3, Eric Morand4, Emmanuelle Maho5, Catharina Lindholm6 and Raj Tummala7, 1University Medical Center and Faculty of Medicine Carl Gustav Carus, TU Dresden, Dresden, Germany, 2University of Manchester and NIHR Manchester Biomedical Research Centre, Manchester University Hospitals NHS Foundation Trust, Manchester Academic Health Science Centre, Manchester, United Kingdom, 3Zucker School of Medicine at Hofstra/Northwell Health, Great Neck, NY, 4Monash University, Melbourne, Australia, 5BioPharmaceuticals R&D, AstraZeneca, Cambridge, United Kingdom, 6BioPharmaceuticals R&D, AstraZeneca, Gothenburg, Sweden, 7BioPharmaceuticals R&D, AstraZeneca, Gaithersburg, MD

    Background/Purpose: The TULIP-1 and TULIP-2 trials of anifrolumab, an anti–type I IFN receptor mAb, enrolled autoantibody-positive (ANA, anti-dsDNA, and/or anti-Smith [anti-Sm]) patients, who fulfilled the…
  • Abstract Number: 1746 • ACR Convergence 2021

    Baricitinib Decreases Anti-dsDNA and IgG Antibodies in Adults with Systemic Lupus Erythematosus from a Phase 2 Double-Blind, Randomized, Placebo-Controlled Trial

    Thomas Dörner1, Ronald Van Vollenhaven2, Andrea Doria3, Bochao Jia4, Damiano Fantini4, Jorge Ross Terres4, Maria Silk5, Stephanie de Bono4, Peter Fischer6 and Daniel Wallace7, 1Charite Universitätsmedizin Berlin and Deutsches Rheumaforschungszentrum (DRFZ), Berlin, Germany, 2University Medical Center, Amsterdam, Netherlands, 3University of Padova, Padova, Italy, 4Eli Lilly and Company, Indianapolis, IN, 5Eli Lilly and Company, Carmel, IN, 6Eli Lilly and Company, North Easton, MA, 7Cedars-Sinai, Los Angeles, CA

    Background/Purpose: Baricitinib (BARI), an oral, selective Janus kinase (JAK)1 and JAK2 inhibitor, improved disease activity in adults with systemic lupus erythematosus (SLE) receiving standard background…
  • Abstract Number: 1801 • ACR Convergence 2021

    The Effect of Ixekizumab versus Adalimumab on Individual Components of the ACR Composite Score, with and Without Concomitant Methotrexate or Other Conventional Synthetic DMARDs at 52 Weeks in Patients with Psoriatic Arthritis

    Elaine Husni1, Sona Kamat2, Keri Stenger3, Rebecca Bolce3, Thorsten Holzkaemper4, Cameron Helt3, So Young Park3, Jeffrey Lisse5 and Luca Idolazzi6, 1Cleveland Clinic, Cleveland, OH, 2St Louis University, Saint Louis, MO, 3Eli Lilly and Company, Indianapolis, IN, 4Eli Lilly and Company, Bad Homburg, Germany, 5Eli Lilly and Company, Tucson, AZ, 6University of Verona, Verona, Italy

    Background/Purpose: It is important to understand how to select among the multiple treatment options for active psoriatic arthritis (PsA). Since individual patient domains may influence…
  • Abstract Number: 1888 • ACR Convergence 2021

    Usefulness of 2019 ACR/EULAR Classification Criteria (AECC) for IgG4-Related Disease Differs Between Clinical Phenotypes of IgG4-RD

    Gözde Kübra Yardımcı1, Bayram Farisogulları2, Gizem Ayan1, Levent Kilic1, Sule Apraş Bilgen1 and Omer Karadag3, 1Hacettepe University, Faculty of Medicine, Department of Internal Medicine, Division of Rheumatology, Ankara, Turkey, 2Division of Rheumatology, Department of Internal Medicine Faculty of Medicine, Hacettepe University, Ankara, Turkey, 3Hacettepe University, Division of Rheumatology, Department of Internal Medicine, Faculty of Medicine, Ankara, Turkey

    Background/Purpose: ACR/EULAR Classification criteria for IgG4-related disease (IgG4-RD) newly published [1]. On the other hand, four distinctive phenotypes of IgG4-RD have been described [2]. We…
  • « Previous Page
  • 1
  • 2
  • 3
  • 4
  • 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 »

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].

Wiley

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

© Copyright 2025 American College of Rheumatology