ACR Meeting Abstracts

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  • Abstract Number: 1433 • ACR Convergence 2022

    A 48-week Analysis of a Pan-EU Real-world Study of SB5 Biosimilar Following Transition from Reference Adalimumab in Patients with Rheumatoid Arthritis, Axial Spondyloarthritis or Psoriatic Arthritis

    Ulf Müller-Ladner1, Karl Gaffney2, Deepak Jadon3, Marco Matucci-Cerinic4, Eugenio Chamizo Carmona5 and Janet Addison6, 1JLU Campus KK, Bad Nauheim, Germany, 2Norfolk and Norwich University Hospital NHS Trust, Norfolk, United Kingdom, 3Cambridge University, Cambridge, United Kingdom, 4University of Florence, Florence, Italy, 5Hospital de Mérida, Mérida, Spain, 6Biogen Idec Ltd, Maidenhead, United Kingdom

    Background/Purpose: SB5, a biosimilar to reference adalimumab (ADL), received marketing authorisation in 2017 (EU) and 2019 (US) based on pre-clinical and clinical phase I and…
  • Abstract Number: 1418 • ACR Convergence 2022

    Change in Disease Activity and Occurrence of Adverse Events After Initiation of Etanercept in Pediatric Patients with Juvenile Psoriatic Arthritis in the CARRA Registry

    Colleen Correll1, Scott Stryker2, David Collier3, Anne Dennos4, Stephen Balevic5, Thomas Phillips5 and Tim Beukelman6, 1University of Minnesota, Minneapolis, MN, 2Amgen Inc., San Francisco, CA, 3Amgen Inc., Simi Valley, CA, 4Duke University, Durham, NC, 5Duke Clinical Research Institute, Durham, NC, 6Childhood Arthritis and Rheumatology Research Alliance (CARRA), Birmingham, AL

    Background/Purpose: Juvenile psoriatic arthritis (JPsA) constitutes ~5% of juvenile idiopathic arthritis (JIA). Several therapeutics are available for JPsA; however, given the low JPsA incidence, important…
  • Abstract Number: 1432 • ACR Convergence 2022

    Pharmacokinetic Evaluation of a Proposed Adalimumab Biosimilar MSB11022 versus the US-Licensed Reference Product: Results of a Randomized, Double-Blind, 3-Arm Parallel-Group, Single-Dose Trial in Healthy Subjects

    Anna Dryja1, Anna Lucia Buccarello2, Isabelle Gaillard2 and Joëlle Monnet2, 1MTZ Clinical Research Sp. z o.o.,, Warsaw, Poland, 2Fresenius Kabi Swiss BioSim, Eysins, Switzerland

    Background/Purpose: Adalimumab, a recombinant fully human monoclonal immunoglobulin G1 antibody, is a biologic directed against tumor necrosis factor-alpha indicated for use in a range of…
  • Abstract Number: 1431 • ACR Convergence 2022

    Impact of Tofacitinib on Fracture Risk in Rheumatoid Arthritis

    Karen E Hansen1, Mahta Mortezavi2, Edward Nagy3, Cunshan Wang4, Carol A Connell4, Zaher Radi5, Heather J Litman6, Giovanni Adami7 and Maurizio Rossini7, 1Rheumatology Division, Department of Medicine, University of Wisconsin School of Medicine and Public Health, Madison, WI, 2Pfizer Inc, New York, NY, 3Pfizer Ltd, Tadworth, United Kingdom, 4Pfizer Inc, Groton, CT, 5Pfizer Inc., Cambridge, MA, 6CorEvitas, LLC, Waltham, MA, 7Rheumatology Unit, Department of Medicine, University of Verona, Verona, Italy

    Background/Purpose: Preclinical data suggest that tofacitinib stimulates osteoblast function and would have a protective effect on bone health and fracture risk in RA.1 We report…
  • Abstract Number: 1427 • ACR Convergence 2022

    Impact of Upadacitinib versus Abatacept on Individual Disease Outcomes in Patients with Rheumatoid Arthritis and Inadequate Responses to Biologic DMARDs

    Ronald van Vollenhoven1, Andrea Rubbert-Roth2, Stephen Hall3, Ricardo Xavier4, Anna K Shmagel5, Yanna Song5, Samuel Anyanwu5 and Vibeke Strand6, 1Amsterdam University Medical Centers, Amsterdam, Netherlands, 2Division of Rheumatology, Cantonal Clinic St Gallen, St.Gallen, Switzerland, 3Emeritus Research and Monash University, Melbourne, Australia, 4Hospital de Clínicas de Porto Alegre, Porto Alegre, Brazil, 5AbbVie, Inc., North Chicago, IL, 6Stanford University School of Medicine, Stanford, CA

    Background/Purpose: The phase 3 SELECT-CHOICE trial of patients with rheumatoid arthritis (RA) and prior inadequate response to biologic DMARD(s) (bDMARD-IR) demonstrated superiority of the JAK…
  • Abstract Number: 1378 • ACR Convergence 2022

    Childhood-onset Systemic Lupus Erythematosus: Long-term Outcomes in a Large Multi-ethnic Ontario Cohort

    Ha-Seul Jeoung1, Kuan Liu1, Roberta Berard2, Wes Fidler3, Janet Pope4, Johannes Roth5, Carter Thorne6, Earl Silverman7 and Deborah Levy8, 1University of Toronto, Toronto, ON, Canada, 2London Health Sciences Centre, London, ON, Canada, 3St. Joseph's Hospital, Thunder Bay, ON, Canada, 4University of Western Ontario, London, ON, Canada, 5University of Ottawa, Ottawa, Canada, 6Southlake Regional Health Centre, Newmarket, ON, Canada, 7The Hospital for Sick Children and University of Toronto, Toronto, ON, Canada, 8Division of Rheumatology, The Hospital for Sick Children; Child Health Evaluative Services, SickKids Research Institute; Department of Paediatrics, University of Toronto, Toronto, ON, Canada

    Background/Purpose: The long-term morbidity and mortality of childhood-onset SLE (cSLE) after transition to adult care is not well documented. The present study aims to fill…
  • Abstract Number: 1410 • ACR Convergence 2022

    Subclinical Atherosclerosis Is Not Related with Acid Uric in Rheumatoid Arthritis: Study of 1005 Patients of a Single University Hospital

    Fabricio Benavides Villanueva1, Cristina Corrales1, Ivan Ferraz Amaro2, Nuria Vegas Revenga3, Ricardo Blanco4, Miguel Angel Gonzalez Gay5 and Alfonso Corrales6, 1Hospital Universitario Marqués de Valdecilla, Santander, Spain, 2Division of Rheumatology. Hospital Universitario de Canarias. Spain., Santa Cruz de Tenerife, Spain, 3Hospital Galdakao- Usansolo, Galdakao, Spain, 4Hospital Universitario Marqués de Valdecilla, IDIVAL, Santander, Spain, 5Hospital Universitario Marques de Valdecilla, Lugo, Spain, 6Research Group on Genetic Epidemiology and Atherosclerosis in Systemic Diseases and in Metabolic Bone Diseases of the Musculoskeletal System, IDIVAL; and Department of Rheumatology, Hospital Universitario Marqués de Valdecilla, Santander, Spain

    Background/Purpose: Rheumatoid Arthritis (RA) and Gout are related with increased cardiovascular (CV) disease. Carotid plaques and increased carotid intima-media thickness (cIMT) are surrogate markers of…
  • Abstract Number: 1423 • ACR Convergence 2022

    Long-Term Treatment with Golimumab Is a Safe Treatment Option Regardless of Risk Factors in Patients with Rheumatoid Arthritis, Psoriatic Arthritis, and Axial Spondyloarthritis: Results from a Real-World Canadian Setting

    Regan Arendse1, Proton Rahman2, Philip Baer3, Derek Haaland4, Dalton Sholter5, Odalis Asin-Milan6, Meagan Rachich7, Emmanouil Rampakakis8, A. Marilise Marrache9 and Allen J. Lehman10, 1Community Rheumatology Care, Saskatoon, Canada, 2Memorial University, St. John's, NL, Canada, 3Baer Weinberg MPC, Scarborough, ON, Canada, 4The Waterside Clinic, Oro Medonte, ON, Canada, 5University of Alberta, Edmonton, AB, Canada, 6Janssen Canada, Laval, QC, Canada, 7Janssen Inc., Guelph, ON, Canada, 8McGill University, Department of Pediatrics and JSS Medical Research, Montréal, QC, Canada, 9Janssen Inc., Dollard-des-Ormeaux, QC, Canada, 10Janssen Inc., Toronto, ON, Canada

    Background/Purpose: Golimumab (GLM), a tumor necrosis factor inhibitor (TNFi), has demonstrated efficacy and a favorable safety profile in inflammatory rheumatic diseases. Recent safety studies with…
  • Abstract Number: 1326 • ACR Convergence 2022

    Impact of COVID-19 Severity on Bone Mineral Density, Sarcopenia and Physical Performance Among Older Adults Following Hospitalization: A Pilot Study

    Diego Cabrera1, Clara Wong2, Andrew Cohen3, Lauren Ferrante3, Alexandra Hajduk3 and Evelyn Hsieh1, 1Section of Rheumatology, Allergy and Immunology, Yale School of Medicine, New Haven, CT, 2Yale School of Public Health, New Haven, CT, 3Yale School of Medicine, New Haven, CT

    Background/Purpose: Altered bone mineral density (BMD), muscle mass and physical performance has been associated with adverse outcomes, however, the effect of COVID-19 on the musculoskeletal…
  • Abstract Number: 1387 • ACR Convergence 2022

    Real-World Utilization of Adalimumab Biosimilar (ABP 501) in Patients with Rheumatoid Arthritis, Ankylosing Spondylitis and Psoriatic Arthritis in Europe

    Ran Jin1, Megan Hughes2, Emily Goddard2, James Piercy2, Delphine Courmier2, Rachael Meadows2 and Waldemar Radziszewski1, 1Amgen, Inc., Thousand Oaks, CA, 2Adelphi Group, Bollington, United Kingdom

    Background/Purpose: ABP 501 is the first adalimumab biosimilar approved by the European Medicines Agency. A clinical trial demonstrated biosimilarity between ABP 501 and the reference…
  • Abstract Number: 1434 • ACR Convergence 2022

    Retrospective Analysis of Tocilizumab-induced Neutropenia in Patients with Rheumatoid Arthritis

    YoungEun Kim1, Soo Min Ahn1, Ji Seon Oh2, Yong Gil Kim1, Chang Keun Lee1, Bin Yoo1 and Seokchan Hong1, 1Department of Rheumatology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea, Seoul, Republic of Korea, 2Department of Information Medicine, Big Data Research Center, Asan Medical Center, Seoul, Republic of Korea

    Background/Purpose: Neutropenia has been reported as one of the most frequent adverse events of tocilizumab. We conducted a retrospective cohort study to determine the risks…
  • Abstract Number: 1419 • ACR Convergence 2022

    Time to Discontinuation and Effectiveness with Baricitinib in Rheumatoid Arthritis: 12-Month European Data from a Multinational, Prospective, Observational Study

    Rieke Alten1, Gerd Burmester2, Marco Matucci-Cerinic3, Andrew Ostor4, Liliana Zaremba-Pechmann5, Tamas Treuer6, Khai Jing Ng6, Jens Gerwien6, Kathryn Gibson7 and Bruno Fautrel8, 1SCHLOSSPARK KLINIK, University Medicine Berlin, Berlin, Germany, 2Charité University Medicine Berlin, Berlin, Germany, 3University of Florence, Florence, Italy, 4Cabrini Hospital, Monash University & Emeritus Research, Melbourne, Australia, 5HaaPACS GmbH, Schriesheim, Germany, 6Eli Lilly and Company, Indianapolis, IN, 7Eli Lilly and Company, Indianapolis, United States of America, Sydney, Australia, 8Sorbonne University Paris, France and Pierre Louis Institute of Epidemiology and Public Health, Paris, France, Paris, France

    Background/Purpose: RA-BE-REAL is a 3-year, multinational, prospective, observational study of adult patients with rheumatoid arthritis (RA) evaluating time to discontinuation of initial RA treatment. Baricitinib…
  • Abstract Number: 1315 • ACR Convergence 2022

    Building Stronger Bones: Optimizing Osteoporosis Screening at a Primary Care Clinic

    Rebecca Pietro1, Shu Min Lao1 and Geeta Varghese2, 1Mount Sinai Morningside West, New York, NY, 2Ryan Chelsea Clinton Clinic, New York, NY

    Background/Purpose: Osteoporosis is a silent disease characterized by low bone mass and deterioration of bone quality, affecting 25% of women.1 The United States Preventive Services…
  • Abstract Number: 1430 • ACR Convergence 2022

    Time to First Remission and Prevalence of Sustained Remission After Etanercept Biosimilar (ETA-B) or Originator (ETA-O) Initiation in Rheumatoid Arthritis

    Cristiano Moura1, Luck Lukusa1, Laura Yan1, Walter P Maksymowych2, Denis Choquette3, Gilles Boire4 and Sasha Bernatsky1, 1Research Institute of the McGill University Health Centre, Montréal, QC, Canada, 2Department of Medicine, University of Alberta, Edmonton, AB, Canada, 3Centre Hospitalier de l'Université de Montréal, Montréal, QC, Canada, 4Universite de Sherbrooke, Sherbrooke, QC, Canada

    Background/Purpose: The first biosimilar etanercept (ETA-B) was approved in Canada in 2016, but real-world data comparing the effectiveness of ETA-B versus its equivalent originator (ETA-O)…
  • Abstract Number: 1398 • ACR Convergence 2022

    Myokine Myostatin Is a Novel Predictor of One-year Radiographic Progression in Patients with Rheumatoid Arthritis

    Jian-Zi Lin, Li-Juan Yang, Hong-Gui Li, Ai-Qi Zeng, Kui-Min Yang and Lie Dai, Department of Rheumatology, Sun Yat-Sen Memorial Hospital, Sun Yat-Sen University, Guangzhou, China

    Background/Purpose: Associations between rheumatoid arthritis (RA) and reduced skeletal muscle have been studied, and we firstly reported myopenia independently predict one-year radiographic progression in RA.…
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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.).

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