ACR Meeting Abstracts

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

  • Abstract Number: 546 • 2018 ACR/ARHP Annual Meeting

    Baricitinib: Early Vs. Delayed Start in Patients with Rheumatoid Arthritis

    Peter C. Taylor1, Yoshiya Tanaka2, Anabela Cardoso3, Jinglin Zhong4, Yun-Fei Chen3, Jennifer Lynn Workman3, Liliana del Carmen Morales5 and Michael Schiff6, 1Botnar Research Centre, Univ of Oxford, Oxford, United Kingdom, 2University of Occupational and Environmental Health, Kitakyushu, Japan, 3Eli Lilly and Company, Indianapolis, IN, 4IQVIA, Morrisville, NC, 5INStituto Reumatologica Strusberg, Cordoba, Argentina, 6University of Colorado, Greenwood Village, CO

    Background/Purpose: Baricitinib (bari) is an oral JAK1/JAK2 inhibitor approved for the treatment of moderately to severely active RA in adults in over 40 countries including…
  • Abstract Number: 886 • 2018 ACR/ARHP Annual Meeting

    Efficacy and Safety of Switching from Adalimumab to Baricitinib: Long-Term Data from Phase 3 Extension Study in Patients with Rheumatoid Arthritis

    Michael E Weinblatt1, Peter C. Taylor2, Edward C. Keystone3, Robert A. Ortmann4, Maher Issa4, Li Xie4, Stephanie de Bono4 and Yoshiya Tanaka5, 1Brigham and Women’s Hospital, Boston, MA, 2Botnar Research Centre, Univ of Oxford, Oxford, United Kingdom, 3Mount Sinai Hospital, Toronto, ON, Canada, 4Eli Lilly and Company, Indianapolis, IN, 5University of Occupational and Environmental Health, Kitakyushu, Japan

    Background/Purpose: Baricitinib (bari) is an oral JAK1/JAK2 inhibitor approved for the treatment of moderately to severely active RA in adults in over 40 countries, including…
  • Abstract Number: 2523 • 2018 ACR/ARHP Annual Meeting

    Rapid Response with Upadacitinib Treatment in Patients with Rheumatoid Arthritis and an Inadequate Response to Csdmards or Bdmards

    Oliver FitzGerald1, Andrea Rubbert-Roth2, Kun Chen3, Sebastian Meerwein4, Jose Jeffrey Enejosa3, Tim Shaw3 and Alvin F. Wells5, 1St. Vincent’s Univ Hospital and Conway Inst Univ College Dublin, Dublin, Ireland, 2Kantonsspital St. Gallen, St Gallen, Switzerland, 3AbbVie Inc., North Chicago, IL, 4AbbVie Deutschland, Ludwigshafen, Germany, 5Rheum and Immunotherapy Ctr, Franklin, WI

    Background/Purpose: Upadacitinib (UPA), an oral JAK inhibitor selective for JAK1, demonstrated efficacy in patients (pts) with moderate to severe rheumatoid arthritis (RA) with an inadequate…
  • Abstract Number: 409 • 2017 ACR/ARHP Annual Meeting

    An Evaluation of Absolute Neutrophil Count As a Biomarker of Inflammatory and Clinical Disease Activity in Baricitinib-Treated Patients

    Iain B. McInnes1, Lee S. Simon2, Robert J. Moots3, Vipin K. Arora4, John D. Bradley4 and David Muram4, 1University of Glasgow, Glasgow, United Kingdom, 2SDG LLC, Cambridge, MA, 3University of Liverpool, Liverpool, UK, Liverpool, United Kingdom, 4Eli Lilly and Company, Indianapolis, IN

    Background/Purpose: Rheumatoid arthritis (RA) patients (pts) tend to have higher absolute neutrophil count (ANC) values compared to healthy individuals.1 Baricitinib (BARI), an oral, selective Janus…
  • Abstract Number: 415 • 2017 ACR/ARHP Annual Meeting

    Baricitinib Reduces GlycA Levels in Phase 2 and Phase 3 Clinical Trials in Patients with Moderate to Severe Rheumatoid Arthritis

    Joel Kremer1, Paul Emery2, Margery A. Connelly3, James D. Otvos4, Steven H. Zuckerman5, Giacomo Ruotolo5, Lei Chen5, Maher Issa5, William L. Macias5 and Iain B. McInnes6, 1Albany Medical College, Albany, NY, 2Leeds MSK Biomed/Chapel Allerton Hospital, Leeds, United Kingdom, 3Laboratory Corporation of America Holdings (LabCorp), Morrisvile, NC, 4Laboratory Corporation of America Holding (LabCorp), Morrisville, NC, 5Eli Lilly and Company, Indianapolis, IN, 6University of Glasgow, Glasgow, United Kingdom

    Background/Purpose: Baricitinib (bari) is an oral selective inhibitor of Janus kinase (JAK) 1/JAK2.1 In the European Union, bari is approved for the treatment of moderate…
  • Abstract Number: 418 • 2017 ACR/ARHP Annual Meeting

    Exploratory Analysis  to Identify Factors Associated with Risk of Structural Progression, Defined As Change from Baseline

    Désirée van der Heijde1, Patrick Durez2, Georg Schett3, Esperanza Naredo4, Mikkel Østergaard5, Gabriella Meszaros6, Pedro Lopez-Romero7, Francesco de Leonardis6 and Roy Fleischmann8, 1Leiden University Medical Center, Leiden, Netherlands, 2UCL-Saint Luc, Bruxelles, Belgium, 3Department of Internal Medicine III, Institute for Clinical Immunology,, Friedrich-Alexander-University Erlangen-Nuremberg (FAU), Erlangen, Germany, 4Hospital Universitario Fundación Jimenez Diaz, Madrid, Spain, 5Glostrup Hospital, Rigshospitalet, Glostrup, Denmark, 6Eli Lilly and Company, Indianapolis, IN, 7Europe Research Center, Eli Lilly and Company, Madrid, Spain, 8University of Texas Southwestern Medical Center, Dallas, TX

    Background/Purpose: Baricitinib (BARI), an oral inhibitor of Janus kinase (JAK)1 and JAK2, is being developed for the treatment of RA. RA-BEGIN (NCT01711359) was a phase…
  • Abstract Number: 502 • 2017 ACR/ARHP Annual Meeting

    Reduction in Disease Activity in Patients with RA and an Inadequate Response to MTX: Baricitinib Compared to Adalimumab and Placebo

    Peter Nash1, Janet E. Pope2, Anabela Cardoso3, Marta Casillas3, Douglas E. Schlichting3, Baojin Zhu3, Scott D. Beattie3 and Josef S. Smolen4, 1University of Queensland, Brisbane, Australia, 2St. Joseph's Health Care, London, ON, Canada, 3Eli Lilly and Company, Indianapolis, IN, 4Rheumatology, Medical University of Vienna, Vienna, Austria

    Background/Purpose: Baricitinib (BARI), is an oral Janus kinase (JAK)1/JAK2 selective inhibitor for treatment of patients with moderately to severely active RA. RA-BEAM was a phase…
  • Abstract Number: 505 • 2017 ACR/ARHP Annual Meeting

    Exposure-Response Analyses of the Effect of Upadacitinib on ACR Responses in the Phase 2b Rheumatoid Arthritis Trials in Patients with Inadequate Response to Methotrexate or to Anti-Tumor Necrosis Factor Therapy

    Ben Klünder1, Mohamed-Eslam F. Mohamed2, Heidi S. Camp2 and Ahmed A. Othman2, 1AbbVie Deutschland GmbH & Co. KG, Ludwigshafen, Germany, 2AbbVie, North Chicago, IL

    Background/Purpose: Upadacitinib, a selective JAK1 inhibitor, demonstrated favorable efficacy in two Phase 2 studies in subjects with moderate to severe rheumatoid arthritis (RA) who had…
  • Abstract Number: 512 • 2017 ACR/ARHP Annual Meeting

    Efficacy Response to Baricitinib Based on Baseline Characteristics in Patients Who Are Inadequate Responders to Conventional DMARD

    Maxime Dougados1, Terence P. Rooney2, Li Xie2, Rena Klar3, Christina L. Dickson2, Ana Pinto Correia2, Yoshiya Tanaka4, Michael Schiff5 and Edward C. Keystone6, 1Department of Rheumatology, Rene Descartes University, Hôpital Cochin, Paris, France, 2Eli Lilly and Company, Indianapolis, IN, 3Quintiles IMS Holdings, Inc., Durham, NC, 4The First Department of Internal Medicine, University of Occupational and Environmental Health, Kitakyushu, Japan, 5University of Colorado, Greenwood Village, CO, 6University of Toronto, Toronto, ON, Canada

    Background/Purpose: Rheumatoid arthritis (RA) is a chronic disease and some patients (pts) have an inadequate response (IR) to conventional DMARDs (csDMARDs). Baricitinib is an oral,…
  • Abstract Number: 513 • 2017 ACR/ARHP Annual Meeting

    Time to Achieve Moderate/Low Disease Activity and Remission in RA Patients on Baricitinib Compared to Adalimumab, Methotrexate, and Placebo

    Edward C. Keystone1, Maxime Dougados2, Eric M. Ruderman3, Baojin Zhu4, Pedro Lopez-Romero5, Hanne Lund6, Anabela Cardoso4, Douglas E. Schlichting4, Pindaro Martinez Osuna4, Robert Ortmann4 and Tore K. Kvien7, 1University of Toronto, Toronto, ON, Canada, 2Rene Descartes University, Cochin Hospital, Paris, France, 3Northwestern University Feinberg School of Medicine, Chicago, IL, 4Eli Lilly and Company, Indianapolis, IN, 5Europe Research Center, Eli Lilly and Company, Madrid, Spain, 6Eli Lilly Norge A.S., Oslo, Norway, 7Diakonhjemmet Hospital, Oslo, Norway

    Background/Purpose: Baricitinib (BARI), an oral, selective Janus kinase (JAK)1/2 inhibitor1, has shown efficacy in DMARD naïve RA patients (pts)2 and in pts with inadequate response…
  • Abstract Number: 530 • 2017 ACR/ARHP Annual Meeting

    Efficacy and Safety of Baricitinib in Patients with Rheumatoid Arthritis: A Meta-Analysis of Randomized Controlled Trials

    Sumit Kunwar1, Christopher E. Collins2 and Florina Constantinescu2, 1Rheumatology, MedStar Washington Hospital Center, washington, DC, 2Rheumatology, MedStar Washington Hospital Center, Washington, DC

    Background/Purpose:  Janus kinases (JAKs) play an important role in intracellular signaling for multiple cytokines in the pathogenesis of RA. Baricitinib is an oral, selective JAK…
  • Abstract Number: 537 • 2017 ACR/ARHP Annual Meeting

    No Effect of Baseline Serum CRP Levels on Clinical Efficacy Parameters in Rheumatoid Arthritis Patients Treated with Filgotinib: Post Hoc Analysis from Two Phase 2B Studies

    Arthur Kavanaugh1, Annegret Van der Aa2, Corinne Jamoul2, Chantal Tasset2, Pille Harrison2 and René Westhovens3, 1Medicine, University of California, San Diego, La Jolla, CA, 2Galapagos NV, Mechelen, Belgium, 3Department of Rheumatology, University Hospitals Leuven, Leuven, Belgium

    Background/Purpose: Filgotinib (GLPG0634, GS-6034) is an oral, selective JAK1 inhibitor that has demonstrated safety and efficacy data in two 24-week placebo-controlled phase 2B studies as…
  • Abstract Number: 1821 • 2017 ACR/ARHP Annual Meeting

    Dose Reduction of Baricitinib in Patients with Rheumatoid Arthritis Achieving Sustained Disease Control: Results of a Prospective Study

    Tsutomu Takeuchi1, Mark C. Genovese2, Boulos Haraoui3, Zhanguo Li4, Li Xie5, Rena Klar6, Ana Pinto Correia5, Susan Otawa5, Pedro Lopez-Romero7, Inmaculada de la Torre5, Terence P. Rooney5 and Josef S. Smolen8, 1Keio University School of Medicine, Tokyo, Japan, 2Stanford University Medical Center, Palo Alto, CA, 3Institut de Rhumatologie de Montreal, Montreal, QC, Canada, 4Peking University People's Hospital, Beijing, China, 5Eli Lilly and Company, Indianapolis, IN, 6Quintiles IMS Holdings, Inc., Durham, NC, 7Europe Research Center, Eli Lilly and Company, Madrid, Spain, 8Medical University of Vienna, Vienna, Austria

    Background/Purpose: In patients (pts) with active RA and inadequate response (IR) to DMARDs, phase 3 studies demonstrated efficacy of baricitinib (2-mg and 4-mg). Larger, more…
  • Abstract Number: 2352 • 2017 ACR/ARHP Annual Meeting

    Cardiovascular Safety during Treatment with Baricitinib in Rheumatoid Arthritis

    Michael Weinblatt1, Peter C. Taylor2, Gerd R. Burmester3, Sarah Witt4, Chadi Saifan4, Chad Walls5, Terence P. Rooney4, Lei Chen4 and Tsutomu Takeuchi6, 1Brigham and Women’s Hospital, Boston, MA, 2NDORMS, University of Oxford, Oxford, United Kingdom, 3Department of Rheumatology and Clinical Immunology, Charité - University Medicine Berlin, Free University and Humboldt University Berlin, Berlin, Germany, 4Eli Lilly and Company, Indianapolis, IN, 5Eli Lilly and C ompany, Indianapolis, IN, 6Keio University School of Medicine, Tokyo, Japan

    Background/Purpose: Baricitinib (BARI) is an oral selective inhibitor of Janus kinase (JAK)1 and JAK2 approved in the EU for the treatment of active RA. Patients…
  • Abstract Number: 1644 • 2016 ACR/ARHP Annual Meeting

    Dose Selection of Filgotinib, a Selective JAK1 Inhibitor, for Rheumatoid Arthritis Phase 3 Studies: Exposure-DAS28 and ACR Modeling Approach

    Namour Florence1, Paul Diderichsen2, Eugène Cox2, Shringi Sharma3 and Chantal Tasset4, 1Galapagos SASU, Romainville, France, 2Quantitative Solutions-Certara, Breda, Netherlands, 3Gilead Sciences, Foster City, CA, 4Galapagos NV, Mechelen, Belgium

    Background/Purpose: Filgotinib is an oral, selective Janus kinase 1 (JAK1) inhibitor showing good efficacy and safety in Phase 2B studies in rheumatoid arthritis (RA) patients. The…
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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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