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Abstracts tagged "Late-Breaking 2025"

  • Abstract Number: LB20 • ACR Convergence 2025

    Efficacy and Safety of Deucravacitinib up to Week 52: A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study in Patients With Active Psoriatic Arthritis Who Are Naive to Biologic Disease-Modifying Antirheumatic Drugs

    Désirée van der Heijde1, Philip Mease2, Carle Paul3, Frank Behrens4, Laure Gossec5, Yuko Kaneko6, Lihi Eder7, Laura Coates8, Andrew Pink9, Weiguo Wan10, Enrique Soriano11, Piotr Leszczyński12, Jose Scher13, Atul Deodhar14, Chahin Pachai15, Janice Li16, Xue Fan16, Sahar Rabbat16, Caroline Sardinas17, Michael Plewinski18, John Vaile19 and Joseph Merola20, 1Leiden University Medical Center, Meerssen, Netherlands, 2Swedish Medical Center/Providence St. Joseph Health, Seattle, Washington, 3Department of Dermatology, INSERM Infinity, Toulouse University, Toulouse, France, 4Goethe-University & Fraunhofer ITMP, Frankfurt, Germany, 5Sorbonne Université, AP-HP & EULAR, Paris, France, 6Division of Rheumatology, Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan, 7University of Toronto, Toronto, Ontario, Canada, 8University of Oxford, Oxford, United Kingdom, 9St John's Institute of Dermatology, Guy's and St Thomas' NHS Foundation Trust and King's College London, London, United Kingdom, 10Huashan Hospital, Fudan University, Shanghai, China (People's Republic), 11Hospital Italiano de Buenos Aires, Buenos Aires, Argentina, 12Department of Internal Medicine and Metabolic Disorders, Poznań University of Medical Sciences, Poznań, Poland, 13New York University School of Medicine, New York, New York, 14Oregon Health & Science University, Portland, Oregon, 15Bristol Myers Squibb, Princeton, New Jersey, 16Bristol Myers Squibb, Princeton, 17Bristol Myers Squibb, garwood, New Jersey, 18Bristol Myers Squibb, Green Brook Township, New Jersey, 19Bristol Myers Squibb, Warren, New Jersey, 20UT Southwestern Medical Center, Dallas, Texas

    Background/Purpose: Deucravacitinib is an oral, selective tyrosine kinase 2 (TYK2) inhibitor being investigated in active PsA in the global, randomized, double-blind, placebo (PBO)-controlled, phase 3…
  • Abstract Number: LB05 • ACR Convergence 2025

    ER Stress-Induced ATP2A3 Drives Rheumatoid Arthritis via Activation of STING Signaling

    yujie cai, Nanfang hospital, Guangzhou, China (People's Republic)

    Background/Purpose: Rheumatoid arthritis (RA) is an autoimmune disease characterized by persistent synovial inflammation and joint bone destruction. Endoplasmic reticulum (ER) stress plays an important role…
  • Abstract Number: LB21 • ACR Convergence 2025

    IDH1/2 Somatic Hotspot Mutations as Independent Drivers of Autoinflammation

    Flore Castellan1, Griffen Mustion2, Mei-Kay Wong1, Kimberly Johansson2, Scott Goldberg1, Yazan Madanat3, Namrata Chandhok4, Abhay Singh5, David Sallman6, Jane Churpek7, Curtis Lachowiez8, Jennifer Yannucci9, Luke Fletcher10, Matthew Schwede11, Amber Afzal2, Yael Kusne12, Alejandro Marinos13, Alexander Coltoff14, Rickey Myhand15, Kiran Vij2, Rosalyn Marar16, Hannah Mitchell2, Maria Stoentcheva2, Giulia Petrone2, Kyra Ddungu2, Hannah Hartman2, Ryan Monahan2, Karen Vandervort2, Jie Liu2, John Cole2, Tibor Kovacsovics17, Hetty Carraway18, Tian Zhang19, Stephen Chung3, Geoffrey Uy2, Eytan Stein20, Devendra Hiwase21, Matthew Walter2, Mrinal Patnaik16, Kelly Bolton22 and David Beck1, 1New York University School of Medicine, New York, New York, 2Washington University School of Medicine, Saint Louis, Missouri, 3UT Southwestern Medical Center, Dallas, Texas, 4University Miami Miller School of Medicine, Miami, Florida, 5Cleveland Clinic, Cleveland, Ohio, 6Moffitt Cancer Center, Tampa, Florida, 7University of Wisconsin School of Medicine, Madison, Wisconsin, 8Oregon Health & Science University, Portland, Oregon, 9Low Country Cancer Care, Savannah, Georgia, 10Willamette Valley Cancer Institute and Research Center, EUgene, Oregon, 11Swedish Health Services, Seattle, Washington, 12Mayo Clinic, Phoenix, Arizona, 13UTSouthwestern Medical Center, Dallas, Texas, 14Medical University of South Carolina, Charleston, South Carolina, 15CovenantOntology & Hematology, Frankfort, Kentucky, 16Mayo Clinic, Rochester, Minnesota, 17City of Hope, Goodyear, Arizona, 18Case Western Reserve University, Cleveland, Ohio, 19Stanford Medicine, Stanford, California, 20Memorial Sloan Kettering Cancer Center, New York, New York, 21Adelaide Medical School, Adelaide, South Australia, Australia, 22Washington University School of Medicine, Saint Louis, Minnesota

    Background/Purpose: Recently, somatic mutations in hematopoietic stem and progenitor cells (HSPCs) have been proposed as a novel mechanism driving systemic inflammation. UBA1 somatic variants in…
  • Abstract Number: LB06 • ACR Convergence 2025

    AgAIN Study: First Head-to-Head Trial of Secukinumab vs. Ustekinumab in TNFα Inhibitor-Experienced Psoriatic Arthritis Patients Reveals Better Efficacy Across Multiple Domains

    Frank Behrens1, Patrizia Sternad2, Klaus Krueger3, Christine App4, Stephanie Lefevre4 and Christiane Schiedel4, 1Department of Rheumatology, Frankfurt University Hospital, Frankfurt, Germany, 2Medizinisches Versorgungszentrum für Rheumatologie Dr. M. Welcker GmbH, Planegg, Germany, 3Rheumatologisches Praxiszentrum, München, Germany, 4Novartis Pharma GmbH, Nürnberg, Germany

    Background/Purpose: Psoriatic arthritis (PsA) patients with prior failure or intolerance to TNFα inhibitors (TNFi) represent a clinically challenging population with limited therapeutic options. The AgAIN…
  • Abstract Number: LB22 • ACR Convergence 2025

    Early Evidence of Proof-of-Concept of an Albumin-DNASE1L3 Fusion Protein (NTR-441) for the Rapid Enzymatic Inactivation of NETs in SLE with DNASE1L3-Deficiency

    Andreas Reiff1, Tadej Avcin2, Bernd Jilma3, Peter Korosec4, Matthias Weiss-Tessbach3, Christian Schoergenhofer3, Masa Bizjak5, Barbara Jenko Bizjan6, Barbara Cugalj Kern5, Kim Simpfendorfer7, Christian Lood8, Tyler Artner9, Angelene Prasanna1, Ken Olivier1, Ghazaleh Gouya1, Ralph Lambalot9, Abdul Hakkim1 and Tobias Fuchs1, 1Neutrolis, Cambridge, Massachusetts, 2University Medical Centre Ljubljana, Ljubljana, Slovenia, 3Medical University of Vienna, Vienna, Austria, 4University Clinic of Respiratory and Allergic Diseases, Golnik, Slovenia, 5University Medical Center Ljubljana, Ljubljana, Slovenia, 6University of Ljubljana, Ljubljana, Slovenia, 7Feinstein Institutes for Medical Research, Manhasset, New York, 8University of Washington, Seattle, Washington, 9Neutrolis, Cambridge

    Background/Purpose: Excessive formation and impaired clearance of Neutrophil Extracellular Traps (NETs) have been linked to autoimmune and inflammatory diseases, notably systemic lupus erythematosus (SLE). DNASE1-like…
  • Abstract Number: LB07 • ACR Convergence 2025

    Adipose-Tissue Derived Mesenchymal Stem Cells vs Hyaluronic Acid in Refractory Knee Osteoarthritis in a low-resource setting: A Phase IIb RCT

    Moshiur Rahman Khasru1, Mohammad Tariqul Islam2, AGM Zakaria Nazimuddin Jubery3, Mahbuba Shirin4, Fazle Rabbi Chowdhury5, Tangila Marzen6, Nafi Uzzaman7, Md Abu Bakar Siddiq8, Md Ashraful Hoque9, Masuda Begum10, Md Moniruzzaman Khan2 and Abul Salek11, 1Musculoskeletal Medicine and Interventional Physiatry Division, Bagladesh Medcial University, Dhaka, Bangladesh, 2Department of Physical Medicine and Rehabilitation, Bangladesh Medical University, Dhaka, Bangladesh, 3Department of Burn and Plastic Surgery, Dhaka Medcial College and Hospital, Dhaka, Bangladesh, 4Department of Radiology and Imaging, Bangladesh Medical University, Dhaka, Bangladesh, 5Department of Internal Medicine, Bangladesh Medical University, Dhaka, Bangladesh, 6Department of Anatomy, Shaheed Suhrawardy Medical College, Dhaka, Bangladesh, 7Stem Cell Rearch Group, Department of Physical Medicine and Rehabilitation, Bangladesh Medical University, Dhaka, Bangladesh, 8Department of Rheumatology, Royal North Shore Hospital, Faculty of Medicine, University of Sydney, New South Wales, Australia, 9Department of Transfusion Medicine, Cumilla Medical College, Cumilla, Bangladesh, 10Department of Haematology, Banglabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh, 11Department of Physical Medicine and Rehabilittaion, Bangladesh Medical University, Dhaka, Bangladesh

    Background/Purpose: Knee osteoarthritis (KOA) is a leading cause of disability, with no available disease-modifying treatments. While Hyaluronic Acid (HA) remains widely used, there is little…
  • Abstract Number: LB23 • ACR Convergence 2025

    A Phase 1 Study of Autologous CAR-Treg Cells in Refractory Rheumatoid Arthritis: Interim Report of Safety and Efficacy

    Minna Kohler1, Sally Arai2, Fawad Aslam3, Gregory Challener4, Matthew Frigault4, Melissa Griffith5, Tamiko Katsumoto6, Elena Massarotti7, Larry Moreland8, Allison Rosenthal9, Jeffrey Sparks7, Janeth Yinh4, Sarah Baxter10, Ari Bitton11, Jason Dubovsky12, Victor Yuan13, Mindy Jensen14, Andrew Clauw15, Gabrielle Furman4, Rita Gyurko7, Megan Hall9, Anna McIntyre4, Jennifer Seifert16, Emma Stainton2, Michelle Blake10, Sabrina Fox-Bosetti13, Herve Lebrec13, Amanda Pace10, Yuanyuan Xiao17, Mei-Lun Wang18, Joe Arron13 and Jeffrey Bluestone19, 1Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, 2Stanford, Palo Alto, California, 3Mayo Clinic, Arizona, Scottsdale, Arizona, 4Massachusetts General Hospital, Boston, Massachusetts, 5University of Colorado Anschutz Medical Campus, Aurora, Colorado, 6Stanford University, Millbrae, California, 7Brigham and Women's Hospital, Boston, Massachusetts, 8University of Colorado, Denver, Colorado, 9Mayo Clinic, Phoenix, Arizona, 10Sonoma Biotherapeutics, Seattle, Washington, 11Sonoma Biotherapeutics, San Diego, California, 12Sonoma Biotherapeutics, Thousand Oaks, California, 13Sonoma Biotherapeutics, South San Francisco, California, 14Sonoma Bio, Seattle, Washington, 15University of Colorado, Aurora, Colorado, 16University of Colorado and Oklahoma Medical Research Foundation, Aurora, Colorado, 17Sonoma Biotherapeutics, Los Altos, California, 18Sonoma Biotherapeutics, San Francisco, California, 19Sonoma Biotherapeutics Inc, South San Francisco, California

    Background/Purpose: Regulatory T cells (Tregs) modulate inflammation, maintain self-tolerance, promote tissue repair, and hold promise as a versatile therapeutic. Autologous polyclonal Tregs have a favorable…
  • Abstract Number: LB08 • ACR Convergence 2025

    Efficacy and Safety of Izokibep, a Novel IL-17A Inhibitor, in Patients with Active Psoriatic Arthritis: Week 52 Results from a Randomized, Double-Blind, Placebo-Controlled, Multicenter, Phase 2b/3 Study

    Philip Mease1, Frank Behrens2, Alan Kivitz3, Edit Drescher4, Piotr Klimiuk5, Howard Sofen6, Nehad Soloman7, Shephard Mpofu8, Fredrik Frejd9 and Peter Taylor10, 1Swedish Medical Center/Providence St. Joseph Health, Seattle, Washington, 2Department of Rheumatology, Frankfurt University Hospital, Frankfurt, Germany, 3Altoona Arthritis and Osteoporosis Center, Altoona Center for Clinical Research, Duncansville, Pennsylvania, 4Vital Medical Center Rheumatology, Veszprém, Hungary, 5Department of Rheumatology and Internal Diseases, Medical University of Bialystok, Bialystok, Poland, 6Department of Medicine/Dermatology, David Geffen UCLA School of Medicine, Los Angeles, California, 7Midwestern University Arizona College of Osteopathic Medicine and Arizona Arthritis and Rheumatology Associates, Phoenix, Arizona, 8ACELYRIN, INC., Agoura Hills, California, 9Affibody Medical AB, Solna, Sweden, 10Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Oxford, United Kingdom

    Background/Purpose: PsA is a chronic, systemic, inflammatory musculoskeletal disease in which dysregulated IL-17A activity plays a pivotal role in disease pathogenesis. Izokibep (IZO) is an…
  • Abstract Number: LB24 • ACR Convergence 2025

    Ianalumab demonstrates significant reduction in disease activity in patients with Sjögren’s disease: Efficacy and safety results from two global Phase 3, randomized, placebo-controlled double-blind studies (NEPTUNUS-1 and NEPTUNUS-2)

    This abstract details will be released on October 25th, 10:00 am CT.
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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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