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 "Late-Breaking 2023"

  • Abstract Number: L10 • ACR Convergence 2023

    Dazodalibep, a CD40L Antagonist, in a Phase 2, Randomized, Double-Blind, Placebo-Controlled, Crossover Trial of Subjects with Sjögren’s Disease Having Unacceptable Symptomatic Burden but Limited Extraglandular Organ Involvement

    E. William St. Clair1, Liangwei Wang2, Ilias Alevizos2, William A. Rees2, Alan N. Baer3, Wan-Fai Ng4, Ghaith Noaiseh5 and Chiara Baldini6, 1Department of Medicine, Duke University Medical Center, Durham, NC, USA, Durham, NC, 2Horizon Therapeutics plc, Rockville, MD, 3Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA, Baltimore, MD, 4Translational and Clinical Research Institute, Newcastle University, Newcastle, United Kingdom, 5Division of Allergy, Clinical Immunology and Rheumatology, Department of Medicine, University of Kansas, Kansas City, KS, USA, Kansas CIty, KS, 6Department of Clinical and Experimental Medicine, Rheumatology Unit, University of Pisa, Pisa, Italy

    Background/Purpose: Dazodalibep (DAZ) is a non-antibody fusion protein that acts as a CD40L antagonist and blocks costimulatory signals between immune cells, including T cells, B…
  • Abstract Number: L11 • ACR Convergence 2023

    Risk of Cardiovascular Events According to Biological Agent Exposure in Patients with Ankylosing Spondylitis: A Korean Population-based Study

    Oh Chan Kwon, Hye Sun Lee, Juyeon Yang, Yong-Beom Park and Min-Chan Park, Yonsei University College of Medicine, Seoul, South Korea

    Background/Purpose: Patients with ankylosing spondylitis (AS) have a higher risk of cardiovascular events than controls. Although biological disease-modifying anti-rheumatic drugs (bDMARDs) are efficacious in treating…
  • Abstract Number: L12 • ACR Convergence 2023

    Efficacy and Safety Outcomes of TAK-279, a Selective Oral Tyrosine Kinase 2 (TYK2) Inhibitor, from a Randomized, Double-blind, Placebo-controlled Phase 2b Trial in Patients with Active Psoriatic Arthritis

    Alan Kivitz1, Elena Tomaselli Muensterman2, Arthur Kavanaugh3, Désirée van der Heijde4, Piotr A. Klimiuk5, Guillermo Valenzuela6, Eva Dokoupilova7, Gabrielle Poirier8, Bhaskar Srivastava8, Sue Dasen8, Xinyan Zhang8, Mona Trivedi2, Haoling Holly Weng9, Ting Hong10, Peter Pothula10 and Xenofon Baraliakos11, 1Altoona Center for Clinical Research, Duncansville, PA, 2Takeda Development Center Americas, Inc., Cambridge, MA, 3Division of Rheumatology, Allergy & Immunology, University of California San Diego Medical School, San Diego, CA, 4Department of Rheumatology, Leiden University Medical Center, Meerssen, Netherlands, 5Department of Rheumatology and Internal Diseases, Medical University of Bialystok and Inter Clinic Piotr Adrian Klimiuk, Białystok, Poland, 6Integral Rheumatology & Immunology Specialists, Plantation, FL, 7Department of Pharmaceutical Technology, Faculty of Pharmacy, Masaryk University and MEDICAL PLUS, s.r.o., Brno and Uherské Hradiště, Czech Republic, 8Nimbus Discovery, Inc., Boston, MA, 9HW MedAdvice LLC, San Diego, CA, 10Takeda Development Center Americas, Inc., Boston, MA, 11Rheumazentrum Ruhrgebiet, Ruhr-University Bochum, Bochum, Germany

    Background/Purpose: TYK2 mediates signaling by key cytokines involved in the pathogenesis of immune-mediated inflammatory diseases such as psoriatic arthritis (PsA) and psoriasis (PsO). TAK-279 is…
  • Abstract Number: L13 • ACR Convergence 2023

    An Open-label, Multicenter, Phase 1/2 Study to Assess Safety, Efficacy and Cellular Kinetics of YTB323, a Rapid Manufacturing CAR-T Cell Therapy Targeting CD19 on B Cells, for Severe Refractory Systemic Lupus Erythematosus: Preliminary Results

    Josefina Cortés Hernández1, Pere Barba2, Mònica Linares Alberich3, Ozana Fischer4, Beata Kovacs4, Thomas Calzascia4, David Pearson4, Ana-Laura Jordán Garrote5, Tiina Kirsilä4, Richard Siegel4, Tamas Shisha4, Giulio Cavalli4 and Peter Gergely4, 1Vall d'Hebron Institute of Research (VHIR) and Hospital Universitari Vall d'Hebron, Universitat Autonoma de Barcelona, Barcelona, Catalonia, Spain, 2Vall d'Hebron Institute of Oncology and Hospital Universitari Vall d'Hebron, Universitat Autonoma de Barcelona, Barcelona, Catalonia, Spain, 3Banc de Sang i Teixits, Hospital Universitari Vall d'Hebron, Barcelona, Catalonia, Spain, 4Novartis Biomedical Research, Basel, Basel-Stadt, Switzerland, 5Novartis Farmacéutica, Barcelona, Catalonia, Spain

    Background/Purpose: Systemic lupus erythematosus (SLE) is characterized by pathogenic autoreactive B cells producing autoantibodies against multiple self-antigens. Recently, a series of clinical cases suggested that…
  • Abstract Number: L16 • ACR Convergence 2023

    Withdrawal of Immunosuppressant and Low-dose Steroids in IgG4-RD Patients with Stable Disease (WInS IgG4-RD): An Investigator-initiated, Multi-center, Open-label, Randomized Controlled Trial

    Linyi Peng1, Yuxue nie1, Jiaxin Zhou1, Lijun Wu2, Fang Wang3, Xiaomei Chen4, Jieqiong Li1, Yu Peng1, Hui Lu1, Lidan Zhao1, Mengtao Li1, Yan Zhao1, Xiaofeng Zeng5, Yunyun Fei1 and Wen Zhang1, 1Peking Union Medical College Hospital,Department of Rheumatology and Clinical Immunology, National Clinical Research Center for Dermatologic and Immunologic Diseases, State Key Laboratory of Complex Severe and Rare Diseases, Beijing, China, 2Xinjiang Uygur Autonomous Region People's Hospital, XinJiang, China, 3Beijing Hospital, Beijing, China, 4Xinjiang Uygur Autonomous Region People's Hospital, Wulumuqi, China, 5Peking Union Medical College Hospital, Chinese Academy of Medical Science & Peking Union Medical College, Beijing, China

    Background/Purpose: IgG4-related disease (IgG4-RD) is a fibroinflammatory disease. Remission induction treatment with glucocorticoid (GC) is usually effective, but its tendency of relapse makes the strategy…
  • « Previous Page
  • 1
  • 2
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