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Abstracts tagged "Janus kinase (JAK)"

  • Abstract Number: 1894 • 2018 ACR/ARHP Annual Meeting

    Baricitinib-Associated Changes in Type l Interferon Gene Signature during a 24-Week Phase-2 Clinical SLE Trial

    Thomas Dörner1, Yoshiya Tanaka2, Michelle Petri3, Josef S. Smolen4, Ernst R. Dow5, Richard E. Higgs5, Robert J. Benschop5, Adam Abel5, Maria E. Silk5, Stephanie de Bono5 and Robert W. Hoffman5, 1Charité Universitätsmedizin Berlin and Deutsches Rheuma-Forschungszentrum (DRFZ), Berlin, Germany, 2University of Occupational and Environmental Health, Kitakyushu, Japan, 3Johns Hopkins University School of Medicine, Baltimore, MD, 4Division of Rheumatology, Department of Medicine 3, Medical University of Vienna, Vienna, Austria, 5Eli Lilly and Company, Indianapolis, IN

    Background/Purpose: In the phase 2 study JAHH (NCT02708095), treatment with baricitinib (bari), an oral selective Janus kinase 1/2 inhibitor approved for the treatment of RA,…
  • Abstract Number: 599 • 2018 ACR/ARHP Annual Meeting

    Comparative Effectiveness in Pain and HAQ-DI Improvement for Baricitinib Versus Adalimumab, Tocilizumab, and Tofacitinib Monotherapies in Csdmard-Naïve Rheumatoid Arthritis Patients: A Matching-Adjusted Indirect Comparison (MAIC)

    Bruno Fautrel1, Baojin Zhu2, Peter C. Taylor3, Mart van de Laar4, Paul Emery5, Francesco de Leonardis2, Carol L. Gaich2, Claudia Nicolay2, Zbigniew Kadziola2, Inmaculada de la Torre6 and Roy Fleischmann7, 1University Pierre et Marie Curie, Paris, France, 2Eli Lilly and Company, Indianapolis, IN, 3Botnar Research Centre, Univ of Oxford, Oxford, United Kingdom, 4Arthritis Centre Twente, University of Twente, Enschede, Netherlands, 5Leeds MSK Biomed/Chapel Allerton Hospital, Leeds, United Kingdom, 6Eli Lilly and Company, Madrid, Spain, 7Metroplex Clinical Research Center, University of Texas Southwestern Medical Center, Dallas, TX

    Background/Purpose: In Phase 3 trial (RA-BEGIN), baricitinib (BARI) monotherapy demonstrated superiority to MTX in pain reduction and HAQ-DI improvement in treatment of csDMARD-naïve active RA…
  • Abstract Number: 2035 • 2018 ACR/ARHP Annual Meeting

    Effect of Baricitinib on Joint-Related Biomarkers in Patients with Moderate-to-Severe Rheumatoid Arthritis

    Christian S. Thudium1, Anne C. Bay-Jensen1, Suntara Cahya2, Ernst R. Dow2, Morten A. Karsdal1, Alisa E. Koch2, Wenling Zhang2 and Robert J. Benschop2, 1Nordic Bioscience, Herlev, Denmark, 2Eli Lilly and Company, Indianapolis, IN

    Background/Purpose: Baricitinib (bari) is an oral selective inhibitor of Janus kinase (JAK) 1 and JAK2. In the phase 3 study RA-BUILD (NCT01721057), once-daily bari yielded…
  • Abstract Number: 887 • 2018 ACR/ARHP Annual Meeting

    Efficacy and Safety of the Novel Oral Janus Kinase (JAK) Inhibitor, Peficitinib (ASP015K), in a Phase 3, Double-Blind, Placebo-Controlled, Randomized Study of Patients with RA Who Had an Inadequate Response to Dmards

    Yoshiya Tanaka1, Tsutomu Takeuchi2, Sakae Tanaka3, Atsushi Kawakami4, Manabu Iwasaki5, Yeong Wook Song6, Yi-Hsing Chen7, Mitsuhiro Rokuda8, Hiroyuki Izutsu8, Satoshi Ushijima8, Yuichiro Kaneko8, Teruaki Shiomi8 and Emi Yamada8, 1University of Occupational and Environmental Health, Kitakyushu, Japan, 2Division of Rheumatology, Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan, 3Nagasaki University, Nagasaki, Japan, 4University of Tokyo, Tokyo, Japan, 5Yokohama City University, Yokohama, Japan, 6Seoul National University Hospital, Seoul, Korea, Republic of (South), 7Taichung Veterans General Hospital, Taichung City, Taiwan, 8Astellas Pharma, Inc., Tokyo, Japan

    Background/Purpose: Peficitinib (ASP015K), a novel oral JAK inhibitor, demonstrated efficacy as once-daily monotherapy in patients with moderate to severe RA in a phase 2b study…
  • Abstract Number: 2065 • 2018 ACR/ARHP Annual Meeting

    Blockade of the JAK/STAT Pathway Inhibits Inflammation and Bone Formation in Two Murine Models of Spondyloarthritis

    Yukiko Maeda1, Zheni Stavre1, Tingting Huang2, Catherine Manning2, Bryant Shaughn3, Michael Macoritto3, Deborah Hyland3, Wendy Waegell3 and Ellen M. Gravallese4, 1Medicine, University of Massachusetts Medical School, Worcester, MA, 2Medicine, University of Massachusetts Medical School, worcester, MA, 3Abbvie Bioresearch Center, worcester, MA, 4Lazare Research Bldg, University of Massachusetts Medical School, Worcester, MA

    Background/Purpose: Spondyloarthritis (SpA) results in significant pain and loss of function due to inflammation and resulting enthesial/periosteal bone formation. Inhibition of the Janus kinase (JAK)/STAT…
  • Abstract Number: 888 • 2018 ACR/ARHP Annual Meeting

    Efficacy and Safety of the Novel Oral Janus Kinase (JAK) Inhibitor, Peficitinib (ASP015K), in a Phase 3, Double-Blind, Placebo-Controlled, Randomized Study of Patients with RA Who Had an Inadequate Response to Methotrexate

    Tsutomu Takeuchi1, Yoshiya Tanaka2, Sakae Tanaka3, Atsushi Kawakami4, Manabu Iwasaki5, Mitsuhiro Rokuda6, Hiroyuki Izutsu6, Satoshi Ushijima6, Yuichiro Kaneko6, Teruaki Shiomi6 and Emi Yamada6, 1Division of Rheumatology, Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan, 2University of Occupational and Environmental Health, Kitakyushu, Japan, 3Nagasaki University, Nagasaki, Japan, 4University of Tokyo, Tokyo, Japan, 5Yokohama City University, Yokohama, Japan, 6Astellas Pharma, Inc., Tokyo, Japan

    Background/Purpose: Peficitinib (ASP015K), a novel oral JAK inhibitor, demonstrated efficacy as once-daily monotherapy in patients with moderate-to-severe RA in a phase 2b study (NCT01649999)1. We…
  • Abstract Number: 2097 • 2018 ACR/ARHP Annual Meeting

    Monotherapy with Filgotinib, a JAK1-Selective Inhibitor, Reduces Disease Severity and Alters Immune Cell Subsets in the NZB/W F1 Murine Model of Lupus

    Pei Han1, Christopher Pohlmeyer1, Ching Shang1, Zhihua Cui2, David Lopez3, Astrid Clarke2, Randall Jones2, Nevena Mollova3, Igor Mikaelian4, David Newstrom3, Shiva Zaboli3, Allyson Shauf3 and Julie Di Paolo5, 1Immunology and Inflammation, Gilead Sciences, Foster City, CA, 2Gilead Sciences, Seattle, WA, 3Gilead Sciences, Foster City, CA, 4Biology Core Support, Gilead Sciences, Foster City, CA, 5Immunology and Inflammation Biology, Gilead Sciences, Inc., Foster City, CA

    Background/Purpose: SLE is a heterogeneous autoimmune disease characterized by immune system hyper-activation leading to the production of autoantibodies and immune attack on multiple organs including…
  • Abstract Number: 889 • 2018 ACR/ARHP Annual Meeting

    Upadacitinib As Monotherapy: A Phase 3 Randomized Controlled Double-Blind Study in Patients with Active Rheumatoid Arthritis and Inadequate Response to Methotrexate

    Josef S. Smolen1, Stanley Cohen2, Paul Emery3, William F C Rigby4, Yoshiya Tanaka5, Ying Zhang6, Alan Friedman6, Ahmed A. Othman6, Heidi S. Camp6 and Aileen L. Pangan6, 1Division of Rheumatology, Department of Medicine 3, Medical University of Vienna, Vienna, Austria, 2Metroplex Clinical Research Center, Dallas, TX, 3Leeds Inst of Rheumatic & Musculoskeletal Medicine, Leeds NIHR BRC, United Kingdom, 4Dartmouth College, Hanover, NH, 5Univ of Occupational and Environmental Health, Kitakyushu, Japan, 6AbbVie, North Chicago, IL

    Background/Purpose: Upadacitinib (UPA), an oral JAK inhibitor, showed efficacy in rheumatoid arthritis (RA) patients (pts) with an inadequate response to csDMARDs or bDMARDs on continuing…
  • Abstract Number: 2103 • 2018 ACR/ARHP Annual Meeting

    Using a Drosophila Model to Unravel the Genetic Complexity of Systemic Lupus Erythematosus

    Nathan Mortimer, Mary Fischer, Ashley Waring and Victoria DeMichel, School of Biological Sciences, Illinois State University, Normal, IL

    Background/Purpose: The objective of our research is to understand the genetic architecture and molecular mechanisms that contribute to the development and progression of the autoimmune…
  • Abstract Number: 890 • 2018 ACR/ARHP Annual Meeting

    A Phase 3, Randomized, Double-Blind Study Comparing Upadacitinib to Placebo and to Adalimumab, in Patients with Active Rheumatoid Arthritis with Inadequate Response to Methotrexate

    Roy Fleischmann1, Aileen L. Pangan2, Eduardo Mysler3, Louis Bessette4, Charles Peterfy5, Patrick Durez6, Andrew Ostor7, Yihan Li2, Yijie Zhou2, Ahmed A. Othman2, In-Ho Song8 and Mark C. Genovese9, 1University of Texas Southwestern Medical Center at Dallas, Metroplex Clinical Research Center, Dallas, TX, 2AbbVie, Inc., North Chicago, IL, 3Organización Medica de Investigación, Buenos Aires, Argentina, 4Laval University, Québec, QC, Canada, 5Spire Sciences LLC, Boca Raton, FL, 6Rheumatology, Rheumatology - Cliniques universitaires Saint-Luc - Université Catholique de Louvain - Institut de Recherche Expérimentale et Clinique (IREC), Brussels, Belgium, 7Cabrini Medical Center, Malvern, Australia, 8AbbVie, Inc., north chicago, IL, 9Stanford University Medical Center, Palo Alto, CA

    Background/Purpose: To assess efficacy, including inhibition of radiographic progression, and safety with upadacitinib (UPA), a JAK1- selective inhibitor, vs placebo (PBO) and active comparator, originator…
  • Abstract Number: 2105 • 2018 ACR/ARHP Annual Meeting

    Genetic Analysis of a Drosophila Systemic Lupus Erythematosus Model Reveals Lupus Susceptibility Genes

    Pooja KR, Brooklynne Thielen, Xavier Hernandez and Nathan Mortimer, School of Biological Sciences, Illinois State University, Normal, IL

    Background/Purpose: Systemic lupus erythematosus (SLE) is a multisystem autoimmune disorder with various immunological abnormalities and a diverse range of clinical symptoms. In contrast to the…
  • Abstract Number: 891 • 2018 ACR/ARHP Annual Meeting

    A Phase 3, Randomized, Controlled Trial Comparing Upadacitinib Monotherapy to MTX Monotherapy in MTX-Naïve Patients with Active Rheumatoid Arthritis

    Ronald van Vollenhoven1, Tsutomu Takeuchi2, Aileen L. Pangan3, Alan Friedman3, Mohamed-Eslam Mohamed4, Su Chen4, Maureen Rischmueller5, Ricardo Blanco6, Ricardo M. Xavier7 and Vibeke Strand8, 1Amsterdam Rheumatology and Immunology Center ARC, Amsterdam, Netherlands, 2Keio University School of Medicine, Tokyo, Japan, 3AbbVie, Inc., North Chicago, IL, 4AbbVie, Inc., North chicago, IL, 5The Queen Elizabeth Hospital and University of Adelaide, Adelaide, Australia, 6Division of Rheumatology, Hospital Universitario Marqués de Valdecilla, Santander, Spain, 7Universidade Federal do Rio Grande do Sul Porto Alegre, Rio Grande do Sul, Brazil, 8Division of Immunology/Rheumatology, Stanford University, Palo Alto, CA

    Background/Purpose: To compare the clinical efficacy, including inhibition of structural damage, and safety of upadacitinib (UPA), a JAK1-selective inhibitor, as monotherapy, vs methotrexate (MTX) monotherapy,…
  • Abstract Number: 2486 • 2018 ACR/ARHP Annual Meeting

    Real-World Outcomes Associated with Triple Therapy Vs. TNFi Combo Therapy: Results from the Corrona Registry

    Jeffrey R. Curtis1, J. Lynn Palmer2, George W. Reed3, Jeffrey Greenberg4, Dimitrios A. Pappas5, Leslie R Harrold6 and Joel Kremer4, 1University of Alabama at Birmingham, Birmingham, AL, 2Corrona Research Foundation, Albany, NY, 3UMass Medical School, Worcester, MA, 4Corrona LLC, Waltham, MA, 5Columbia University, New York, NY, 6University of Massachusetts Medical School, Worcester, MA

    Background/Purpose: Despite several randomized controlled trials showing comparable clinical outcomes with triple therapy (Triple; MTX, SSZ, HCQ) versus combination therapy with MTX+TNFi (TNFi Combo), the…
  • Abstract Number: 962 • 2018 ACR/ARHP Annual Meeting

    Safety Profile of Baricitinib for the Treatment of Rheumatoid Arthritis up to 6 Years: An Updated Integrated Safety Analysis

    Mark C. Genovese1, Josef S. Smolen2, Tsutomu Takeuchi3, Terence P. Rooney4, Christina L. Dickson4, Xiao-Yan Yang4, Chadi Saifan4, Anabela Cardoso4, Maher Issa4, Taeko Ishii5 and Kevin Winthrop6, 1Stanford University Medical Center, Palo Alto, CA, 2Division of Rheumatology, Department of Medicine 3, Medical University of Vienna, Vienna, Austria, 3Division of Rheumatology, Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan, 4Eli Lilly and Company, Indianapolis, IN, 5Eli Lilly and Company, Kobe, Japan, 6Oregon Health and Science University, Portland, OR

    Background/Purpose:  Baricitinib (bari), an oral, selective inhibitor of Janus kinase (JAK) 1 and JAK 2, is approved for the treatment of moderately to severely active…
  • Abstract Number: 2517 • 2018 ACR/ARHP Annual Meeting

    The JAK1-Selective Inhibitor Filgotinib Reverses the Disease-Associated Transcriptional Profile Found in the Blood of Patients with Active Rheumatoid Arthritis

    Peter C. Taylor1, Bryan Downie2, Luting Zhuo2, Yevgeniy Gindin2, Jacqueline Tarrant3, Jinfeng Liu2, René Galien4 and Amer M Mirza5, 1University of Oxford Botnar Research Centre, Kennedy Institute of Rheumatology, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, Oxford, United Kingdom, 2Bioinformatics, Gilead Sciences Inc., Foster City, CA, 3Gilead Sciences Inc., Foster City, CA, 4Galapagos SASU, Romainville, France, 5Biomarker Sciences, Gilead Sciences Inc., Foster City, CA

    Background/Purpose: Filgotinib (FIL), an oral JAK1- selective inhibitor, has shown good safety and efficacy in active rheumatoid arthritis (RA) patients with inadequate response to MTX…
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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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