ACR Meeting Abstracts

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Abstracts tagged "Janus kinase (JAK) and rheumatoid arthritis"

  • Abstract Number: 46 • 2019 ACR/ARP Annual Meeting

    Key Inflammatory Biomarkers at Baseline Are Associated with Filgotinib Response at Week 12 in Rheumatoid Arthritis Patients with Inadequate Response or Intolerance to Biologic DMARDs

    Peter Taylor1, Emon Elboudwarej 2, Bryan Downie 3, Rachael Hawtin 2, Jinfeng Liu 2 and Amer M. Mirza 2, 1University of Oxford, Oxford, United Kingdom, 2Gilead Sciences, Inc., Foster City, CA, 3Gilead Sciences, Inc., Foster Citty, CA

    Background/Purpose: Filgotinib (FIL), an oral, selective, Janus Kinase 1 (JAK1) inhibitor was effective in Phase 3 studies of active RA in patients (pts) with inadequate…
  • Abstract Number: 1329 • 2019 ACR/ARP Annual Meeting

    Pooled Safety Analyses from Phase 3 Studies of Filgotinib in Patients with Rheumatoid Arthritis

    Kevin Winthrop1, Mark Genovese 2, Bernard Combe 3, Yoshiya Tanaka 4, Alan Kivitz 5, Franziska Matzkies 6, Beatrix Bartok 6, Lei Ye 6, Ying Guo 6, Chantal Tasset 7, John Sundy 6, Edward Keystone 8, Rene Westhovens 9, William F.C. Rigby 10 and Gerd Burmester 11, 1Oregon Health and Science University, Portland, OR, 2Stanford University, Stanford, CA, 3CHU Montpellier, Montpellier University, Montpellier, France, 4University of Occupational and Environmental Health Japan, Kitakyushu, Japan, 5Altoona Center for Clinical Research, Duncansville, PA, 6Gilead Sciences, Inc., Foster City, CA, 7Galapagos NV, Mechelen, Belgium, 8Mount Sinai Hospital and University of Toronto, Toronto, Canada, 9University Hospitals, Leuven, Belgium, 10Dartmouth College, Lebanon, NH, 11Charité—University Medicine Berlin, Berlin, Germany

    Background/Purpose: Filgotinib (FIL) is an orally administered, selective inhibitor of Janus Kinase 1 (JAK1) that is under development for the treatment of RA and other…
  • Abstract Number: 574 • 2018 ACR/ARHP Annual Meeting

    Longitudinal Efficacy Analysis of Patients with Active Rheumatoid Arthritis and Inadequate Response to Conventional Synthetic Dmards: Response Following Rescue from Baricitinib 2mg to 4mg Once-Daily

    Roy Fleischmann1, Mark C. Genovese2, Anabela Cardoso3, Luna Sun3, Yun-Fei Chen3, Chad D. Walls3, Douglas E. Schlichting3, Tsutomu Takeuchi4, Maxime Dougados5, Josef S. Smolen6 and Jeffrey R. Curtis7, 1Metroplex Clinical Research Center, University of Texas Southwestern Medical Center, Dallas, TX, 2Stanford University Medical Center, Palo Alto, CA, 3Eli Lilly and Company, Indianapolis, IN, 4Keio University School of Medicine, Tokyo, Japan, 5Paris Descartes University, Hôpital Cochin, Paris, France, 6Division of Rheumatology, Department of Medicine 3, Medical University of Vienna, Vienna, Austria, 7University of Alabama at Birmingham, Birmingham, AL

    Background/Purpose: Baricitinib (bari), an oral selective Janus kinase 1/2 inhibitor, has shown clinical efficacy in patients (pts) with RA and an inadequate response to conventional…
  • Abstract Number: 2826 • 2014 ACR/ARHP Annual Meeting

    A Phase 2b, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled, Dose-Finding, Multi-Center Study to Evaluate the Safety and Efficacy of ASP015K in Moderate to Severe Rheumatoid Arthritis Subjects Not on Concomitant Methotrexate

    Mark C. Genovese1, Maria Greenwald2, Christine Codding3, Mario H. Cardiel4, Anna Zubrzycka-Sienkiewicz5, Alan J. Kivitz6, Steve Wisseh7, Kathyjo Shay8 and Jay P. Garg8, 1Division of Immunology and Rheumatology, Stanford University Medical Center, Palo Alto, CA, 2Desert Medical Advances, PALM DESERT, CA, 3Health Research of Oklahoma, Oklahoma City, OK, 4Centro de Investigacion Clinica de Morelia, Morelia, Mexico, 5ARS Rheumatica sp. Zo.o, Reumatika, Warszawa, Poland, 6Altoona Center for Clinical Research, Duncansville, PA, 7Biocis, Chicago, IL, 8Astellas Pharma Global Development, Northbrook, IL

    Background/Purpose ASP015K is a novel oral Janus kinase (JAK) inhibitor in development for the treatment of rheumatoid arthritis (RA). ASP015K inhibits JAK 1/3 with relative…
  • Abstract Number: 948 • 2014 ACR/ARHP Annual Meeting

    A Phase 2b, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled, Dose-Finding, Multi-Center Study to Evaluate the Safety and Efficacy of ASP015K in Moderate to Severe Rheumatoid Arthritis Subjects Who Have Had an Inadequate Response to Methotrexate

    Alan J. Kivitz1, Anna Zubrzycka-Sienkiewicz2, Sergio R. Gutierrez-Ureña3, Jeffrey Poiley4, Rita Kristy5, Kathyjo Shay5 and Jay P. Garg5, 1Altoona Center for Clinical Research, Duncansville, PA, 2ARS Rheumatica sp. Zo.o, Reumatika, Warszawa, Poland, 3Hospital Civil de Guadalajara FAA, CUCS UdG, Guadalajara, Mexico, 4Arthritis Associates, Orlando, FL, 5Astellas Pharma Global Development, Northbrook, IL

    Background/Purpose ASP015K is a novel oral Janus kinase (JAK) inhibitor in development for the treatment of rheumatoid arthritis (RA). ASP015K inhibits JAK 1/3 with relative…
  • Abstract Number: L12 • 2012 ACR/ARHP Annual Meeting

    Short- and Long-Term Efficacy of Tofacitinib, an Oral Janus Kinase Inhibitor, in the Treatment of Patients with Rheumatoid Arthritis and an Inadequate Response to TNF Inhibitors: Analyses of Pooled Phase 2, Phase 3, and Long-Term Extension Studies

    G. Burmester1, Ricardo Blanco2, Andrea Rubbert-Roth3, Thijs Hendrikx4, Kenneth Kwok5, John Bradley6, Samuel H. Zwillich6, Birgitta Benda7 and Charles A. Mebus6, 1Department of Medicine/Rheumatology and Clinical Immunology and German Rheumatism Research Centre Berlin (DRFZ), Charité University Medicine Berlin, Berlin, Germany, 2Rheumatology, Hospital Universitario Marques De Valdecilla, Santander, Spain, 3Internal Medicine I, University of Cologne, Cologne, Germany, 4Pfizer bv, Capelle aan den IJssel, Netherlands, 5Pfizer Inc, New York, NY, 6Pfizer Inc, Groton, CT, 7Pfizer Inc., Collegeville, PA

    Background/Purpose: Tofacitinib is a novel, oral Janus kinase inhibitor investigated as a targeted immunomodulator and disease-modifying therapy for rheumatoid arthritis (RA). The efficacy and safety…
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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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