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  • Abstract Number: 524 • 2019 ACR/ARP Annual Meeting

    A Comparison of Upadacitinib Plus Methotrexate and Upadacitinib Plus Other CsDMARDs in Patients with Rheumatoid Arthritis: An Analysis of Two Phase 3 Studies

    Joel Kremer1, Filip Van den Bosch 2, Andrea Rubbert-Roth 3, Sebastiao Radominski 4, Gerd Burmester 5, Heidi Camp 6, Sebastian Meerwein 7, Mark Howard 8, Yanna Song 9, Sheng Zhong 10 and Bernard Combe 11, 1Albany Medical College, Albany, NY, 2Ghent University Hospital, Ghent, Belgium, 3Kantonsspital St. Gallen, St Gallen, Switzerland, 4Universidade Federal do Paraná, Curitiba, Brazil, 5Charité—University Medicine Berlin, Berlin, Germany, 6AbbVie Inc., North Chicago, IL, 7AbbVie GmbH Co. KG, Ludwigshafen, Germany, Wiesbaden, Germany, 8AbbVie Inc., North Chicago, 9AbbVie Inc., North Chicago, IL, USA, North Chicago, 10AbbVie Inc., North Chicago, IL, USA, North Chicago, IL, 11CHU Montpellier, Montpellier University, Montpellier, France

    Background/Purpose: Upadacitinib (UPA), a selective JAK1 inhibitor, has shown efficacy in patients with rheumatoid arthritis (RA) when combined with methotrexate (MTX) or other conventional synthetic…
  • Abstract Number: 525 • 2019 ACR/ARP Annual Meeting

    Factors Associated with Persistent Drug-free Remission in Patients with Rheumatoid Arthritis

    Larissa Valor1, Melanie Hagen 2, Michaela Reiser 3, Fabian Hartmann 3, Arnd Kleyer 2, Bernhard Manger 4, Georg Schett 5, Jürgen Rech 6 and Koray Tascilar 7, 1Friedrich-Alexander-University Erlangen-Nürnberg. Department of Internal Medicine 3 - Rheumatology and Immunology. Erlangen., Erlangen, Germany, 2Department of Internal Medicine 3 – Rheumatology and Immunology, Friedrich-Alexander-University Erlangen-Nürnberg, University Hospital Erlangen, Erlangen, Germany, Erlangen, Germany, 3Department of Internal Medicine 3, Friedrich-Alexander-University Erlangen-Nuremberg (FAU) and Universitätsklinikum Erlangen, Erlangen, Bayern, Germany, 4Friedrich-Alexander-University Erlangen-Nürnberg. Department of Internal Medicine 3 - Rheumatology and Immunology. Erlangen. Germany., Erlangen, Germany, 5Department of Internal Medicine 3, Friedrich Alexander University Erlangen-Nuremberg, Erlangen, Germany, 6Department of Internal Medicine 3, Friedrich-Alexander-University Erlangen-Nuremberg (FAU) and Universitätsklinikum Erlangen, Erlangen, Germany, 7Department of Internal Medicine 3 – Rheumatology and Immunology, Friedrich-Alexander-University Erlangen-Nürnberg, University Hospital Erlangen, Erlangen, Germany, Erlangen, Bayern, Germany

    Background/Purpose: Persistent drug-free remission of RA is a condition close to “cure” of the disease. Long-term drug-free remission is considered rare and challenging to reach,…
  • Abstract Number: 526 • 2019 ACR/ARP Annual Meeting

    Factors Influencing Discontinuation in Long-term RA Treatment

    Madison Grinnell1, Sofia Pedro 2 and Kaleb Michaud 3, 1University of Nebraska College of Medicine, OMAHA, NE, 2FORWARD, The National Databank for Rheumatic Diseases, Wichita, KS, 3University of Nebraska Medical Center, Omaha, NE

    Background/Purpose: While medication persistence can act as a substitute metric for effectiveness, few studies have examined real-world patterns of bDMARD persistence by line of treatment…
  • Abstract Number: 527 • 2019 ACR/ARP Annual Meeting

    Safety and Effectiveness of Upadacitinib or Adalimumab in Patients with Rheumatoid Arthritis: Results at 48 Weeks

    Roy Fleischmann1, Jose Jeffrey Enejosa 2, In-Ho Song 3, Eduardo Mysler 4, Louis Bessette 5, Charles Peterfy 6, Patrick Durez 7, Andrew Östör 8, Yijie Zhou 9 and Mark Genovese 10, 1Metroplex Clinical Research Center and University of Texas Southwestern Medical Center, Dallas, TX, 2AbbVie Inc., North Chicago, IL, 3AbbVie Inc., North Chicago, IL, USA, North Chicago, IL, 4Organización Medica de Investigación, Buenos Aires, Argentina, Buenos Aires, Argentina, 5Laval University, Quebec City, QC, Canada, 6Spire Sciences Inc, Boca Raton, 7Pôle de Recherche en Rhumatologie, Institut de Recherche Expérimentale et Clinique, UCL Saint-Luc, Brussels, Belgium, 8Cabrini Medical Centre, Monash University, Malvern, Australia, Malvern, Australia, 9AbbVie Inc., North Chicago, 10Stanford University, Stanford, CA

    Background/Purpose: In the SELECT-COMPARE study in rheumatoid arthritis (RA) patients (pts) with inadequate response to methotrexate (MTX), upadacitinib (UPA), a JAK1- selective inhibitor, was superior…
  • Abstract Number: 528 • 2019 ACR/ARP Annual Meeting

    Assessment of Bone and Cartilage Turnover Markers Following Treatment with Repository Corticotropin Injection in Patients with Persistently Active Rheumatoid Arthritis

    Roy Fleischmann1, Daniel Furst 2, Erin Connolly-Strong 3, Jingyu Liu 3, Julie Zhu 3 and Richard Brasington 4, 1Metroplex Clinical Research Center and University of Texas Southwestern Medical Center, Dallas, TX, 2University of California, Los Angeles, CA, 3Mallinckrodt Pharmaceuticals, ARD, LLC, Bedminster, NJ, 4Washington University School of Medicine in St Louis, St Louis, MO

    Background/Purpose: Persistently active rheumatoid arthritis (RA) is an autoimmune disorder characterized by chronic inflammation and bone loss.1 Although short-term administration of corticosteroids (CSs) is recommended…
  • Abstract Number: 529 • 2019 ACR/ARP Annual Meeting

    Characterization of Remission in Patients with Rheumatoid Arthritis Treated with Upadacitinib or Comparators

    Stephen Hall1, Tsutomu Takeuchi 2, Glen Thomson 3, Paul Emery 4, Bernard Combe 5, Andrea Everding 6, Karel Pavelka 7, Yanna Song 8, Tim Shaw 9, Alan Friedman 9, In-Ho Song 10 and Eduardo Mysler 11, 1Monash University and Emeritus Research, Melbourne, Australia, 2Keio University School of Medicine, Tokyo, Japan, 3CIADS Research, Winnipeg, Canada, 4Leeds Institute of Rheumatic and Musculoskeletal Medicine, Leeds, United Kingdom, 5CHU Montpellier, Montpellier University, Montpellier, France, 6HRF Hamburger Rheuma Forschungszentrum, Hamburg, Germany, 7Institute of Rheumatology, Department of Rheumatology, 1st Faculty of Medicine, Prague, Czech Republic, Prague 2, Czech Republic, 8AbbVie Inc., North Chicago, IL, USA, North Chicago, 9AbbVie Inc., North Chicago, 10AbbVie Inc., North Chicago, IL, USA, North Chicago, IL, 11Organización Medica de Investigación, Buenos Aires, Argentina, Buenos Aires, Argentina

    Background/Purpose: Across all phase 3 studies, treatment with upadacitinib (UPA), a JAK1-selective inhibitor, was associated with significantly higher remission (REM) rates, compared to placebo (PBO)…
  • Abstract Number: 530 • 2019 ACR/ARP Annual Meeting

    Phase I Evaluation of the PDE4 Inhibitor LY2775240: Head to Head Comparison with Apremilast Using an Ex Vivo Pharmacodynamic Assay

    Daniel Dairaghi1, Karen Cox 1, Stephen Ho 1, Paul Klekotka 2, Diane Phillips 1, Jean Lim 3, Shweta Urva 1 and Dipak Patel 2, 1Eli Lilly and Company, Indianapolis, IN, 2Eli Lilly and Company, San Diego, CA, 3Eli Lilly and Company, singapore, Singapore

    Background/Purpose: LY2775240 is a potent and selective phosphodiesterase (PDE4) inhibitor being investigated as a potential treatment for inflammatory disorders, such as psoriasis. PDE4 is expressed…
  • Abstract Number: 531 • 2019 ACR/ARP Annual Meeting

    Efficacy and Safety of Gonadotropin-Releasing Hormone Antagonism in Severe Biologic Refractory Rheumatoid Arthritis

    Anita Kass1, Hans Christian Gulseth 1 and Camilla Zettel 1, 1Betanien Hospital, Skien, Norway

    Background/Purpose: The pathogenesis of rheumatoid arthritis (RA) is unclear, and additional therapeutic approaches are needed. The improvement of RA disease activity during pregnancy, and flares during the…
  • Abstract Number: 532 • 2019 ACR/ARP Annual Meeting

    A Phase 2 Study of E6011, an Anti-Fractalkine Monoclonal Antibody, ㏌ Patients with Rheumatoid Arthritis Inadequately Responding to Biologics

    Yoshiya Tanaka1, Tsutomu Takeuchi 2, Hisashi Yamanaka 3, Toshihiro Nanki 4, Hisanori Umehara 5, Nobuyuki Yasuda 6, Fumitoshi Tago 7, Yasumi Kitahara 8, Makoto Kawakubo 7, Hayato Hisaki 8, Seiichiro Hojo 8, Tetsu Kawano 6 and Toshio Imai 6, 1University of Occupational and Environmental Health Japan, Kitakyushu, Japan, 2Keio University School of Medicine, Tokyo, Japan, 3Sanno Medical Center, Minato-ku, Tokyo, Japan, 4Division of Rheumatology, Department of Internal Medicine, School of Medicine, Faculty of Medicine, Toho University, Tokyo, Japan, 5Nagahama City Hospital / Division of Rheumatology and Immunology, Nagahama, Japan, 6KAN Research Institute, Inc., Kobe, Japan, 7Eisai Co., Ltd., Tokyo, Japan, 8Eisai Co., Ltd., Bunkyo-ku, Japan

    Background/Purpose: Fractalkine (CX3CL1, designated as FKN hereafter) is the sole member of the CX3C-chemokine which leads to dual actions, chemotaxis and cell adhesion for leukocytes…
  • Abstract Number: 533 • 2019 ACR/ARP Annual Meeting

    Impact of Formulary Change on TNFi Treatment Patterns and Healthcare Utilization Costs in RA Patients

    Jennifer Schenfeld1, Scott Stryker 2, Hafiz Oko-osi 1 and Bradley Stolshek 2, 1Amgen, Inc, Thousand Oaks, CA, 2Amgen Inc., Thousand Oaks, CA

    Background/Purpose: Changes in formulary tiers can potentially have unintended impact on outcomes. Moderate-to-severe rheumatoid arthritis (RA) is often treated with Tumor Necrosis Factor inhibitors (TNFi).…
  • Abstract Number: 534 • 2019 ACR/ARP Annual Meeting

    CXCL13 Serum Levels and Circulating Follicular Helper T-Cells Decrease After Co-stimulation Blockade with Abatacept in Rheumatoid Arthritis

    Silvia Piantoni1, Francesca Regola 2, Laura Andreoli 3, Angela Tincani 3 and Paolo Airò 4, 1ASST Spedali Civili and University of Brescia, Brescia, Italy, 2Rheumatology and Clinical Immunology Unit, ASST Spedali Civili and University of Brescia, Brescia, Italy, Brescia, Italy, 3Rheumatology and Clinical Immunology, Spedali Civili and Department of Clinical and Experimental Sciences, University of Brescia, Brescia, Italy, Brescia, Italy, 4UO Reumatologia e Immunologia Clinica, Spedali Civili di Brescia, Brescia, Italy, Brescia, Italy

    Background/Purpose: CXCL13 chemokine, by interacting with CXCR5 receptor, attracts B-lymphocytes and CD4+CXCR5+ICOS+ follicular helper T-lymphocytes (THFs) in lymphoid follicles. In rheumatoid arthritis (RA) CXCL13 is…
  • Abstract Number: 535 • 2019 ACR/ARP Annual Meeting

    Exploratory Analysis of a Phase 2b Study Confirms Substantial Pain Improvement with Anti-GM-CSF Monoclonal Antibody Otilimab (GSK3196165) in Patients (Pts) with Active RA

    Christopher D. Buckley1, Jesus A. Simon Campos 2, Vyacheslav Zhdan 3, Brandon Becker 4, Olivier Collignon 5, Carol Hawkes 6, Mark Layton 7, Jatin Patel 8, Katherine Davy 7, Anubha Gupta 7 and Sofia Fernandes 5, 1Rheumatology Research Group, University of Birmingham, Birmingham, United Kingdom, 2Köhler & Milstein Research, Mérida, Mexico, 3M.V. Sklifosovskyi Poltava Regional Clinical Hospital, Poltava, Ukraine, 4GSK, Upper Providence, PA, 5GSK, Stevenage, United Kingdom, 6GSK, Stockley Park, United Kingdom, 7GlaxoSmithKline, Stevenage, United Kingdom, 8GlaxoSmithKline, Stockley Park, United Kingdom

    Background/Purpose: Treatment of pain remains a priority for patients (pts) with RA. Otilimab (GSK3196165) is a human mAb that inhibits GM-CSF, a key driver in…
  • Abstract Number: 536 • 2019 ACR/ARP Annual Meeting

    PERFUSE: A French Prospective/Retrospective Non-interventional Cohort Study of Infliximab-naïve and Transitioned Patients Receiving Infliximab Biosimilar SB2; An Interim Analysis

    Bruno Fautrel1, Yoram Bouhnik 2, Guillaume Desjeux 3, Ulrich Freudensprung 4, Janet Addison 5 and Amira Brigui 6, 1Pitié-Salpêtrière Hospital, Department of Rheumatology, AP-HP, Sorbonne University, UPMC university, Paris, Ile-de-France, France, 2Beaujon Hospital, Department of Gastroenterology, AP-HP, Paris Diderot University, Clichy, France, 3E-health Services Sanoïa, Digital CRO, Gémenos, France, 4Biogen International GmbH, Zug, Switzerland, 5Biogen UK, Maidenhead, United Kingdom, 6Biogen France SAS, Paris, France

    Background/Purpose: SB2 is approved in the EU as an infliximab (IFX) biosimilar, having demonstrated bioequivalence and similar efficacy, safety and immunogenicity as the reference. There…
  • Abstract Number: 537 • 2019 ACR/ARP Annual Meeting

    Efficacy and Safety Results from a Randomized Double-Blind Study That Compared the Proposed Biosimilar ABP 798 with Rituximab in Subjects with Moderate to Severe RA

    Gerd Burmester1, Edit Drescher 2, Pawel Hrycaj 3, David Chien 4, Zhiying Pan 4 and Stanley Cohen 5, 1Charité—University Medicine Berlin, Berlin, Germany, 22Veszprém Csolnoky Ferenc County Hospital, Veszprém, Hungary, 3Koscian Municipal Hospital, Koscian, Poland, 4Amgen, Thousand Oaks, CA, 5Metroplex Clinical Research Center, Dallas, TX

    Background/Purpose: ABP 798 is being developed as a biosimilar to rituximab, a CD20-directed cytolytic antibody that is approved in the US and EU for treatment…
  • Abstract Number: 538 • 2019 ACR/ARP Annual Meeting

    Long-Term Safety and Efficacy of Upadacitinib in Patients with Rheumatoid Arthritis and an Inadequate Response to CsDMARDs: Results at 60 Weeks

    Gerd Burmester1, Filip Van den Bosch 2, Louis Bessette 3, Alan Kivitz 4, Yihan Li 5, Alan Friedman 6, Aileen Pangan 6, Heidi Camp 5 and Joel Kremer 7, 1Charité—University Medicine Berlin, Berlin, Germany, 2Ghent University Hospital, Ghent, Belgium, 3Laval University, Quebec City, QC, Canada, 4Altoona Center for Clinical Research, Duncansville, PA, 5AbbVie Inc., North Chicago, IL, 6AbbVie Inc., North Chicago, 7Albany Medical College, Albany, NY

    Background/Purpose: Upadacitinib (UPA), an oral, JAK1-selective inhibitor showed efficacy over 12 weeks (wks) in patients (pts) with moderately to severely active rheumatoid arthritis (RA) and…
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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 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.).

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