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Abstracts tagged "Janus kinase (JAK)"

  • Abstract Number: L3 • 2013 ACR/ARHP Annual Meeting

    A Phase 2b, 12-Week Study of VX-509, an Oral Selective Janus Kinase 3 Inhibitor, in Combination with Background Methotrexate in Rheumatoid Arthritis

    MC Genovese1, Ronald van Vollenhoven2, Bradley J. Bloom3, John G. Jiang3 and Nils Kinnman4, 1Stanford University, Palo Alto, CA, 2Karolinska Institute, Stockholm, Sweden, 3Vertex Pharmaceuticals Incorporated, Cambridge, MA, 4Vertex Pharmaceuticals Incorporated, Eysins, Switzerland

    Background/Purpose: VX-509 is an oral selective JAK3 inhibitor being evaluated for the treatment of rheumatoid arthritis (RA). The objective of this 24-week, randomized, placebo-controlled, double-blind,…
  • Abstract Number: 2329 • 2013 ACR/ARHP Annual Meeting

    Improvements In Physical Function Correlate With Improvements In Health Related Quality Of Life: Reported Outcomes In Rheumatoid Arthritis Patients Treated With Tofacitinib: Results From 3 Randomized Phase 3 Trials

    V. Strand1, R. E. Alten2, C. I. Nduaka3, R. Riese3, D. Gruben3, S. H. Zwillich3, J. Andrews3 and G. Wallenstein3, 1Adjunct, Division of Immunology / Rheumatology, Stanford University, Palo Alto, CA, 2Department of Internal Medicine II, Schlosspark-Klinik, University Medicine, Berlin, Germany, 3Pfizer Inc, Groton, CT

    Background/Purpose: Tofacitinib is a novel, oral Janus kinase (JAK) inhibitor for the treatment of rheumatoid arthritis (RA). RA affects all domains of health-related quality of…
  • Abstract Number: 2330 • 2013 ACR/ARHP Annual Meeting

    Relationship Between Lymphocyte Count and Risk Of Infection In Rheumatoid Arthritis Patients Treated With Tofacitinib

    R. F. van Vollenhoven1, R. Riese2, S. Krishnaswami2, T. Kawabata2, C. Fosser2, S. Rottinghaus2, M. Lamba2 and S. H. Zwillich2, 1Clinical Trials Unit Department of Rheumatology, The Karolinska Institute, Stockholm, Sweden, 2Pfizer Inc, Groton, CT

    Background/Purpose: Tofacitinib is a novel oral Janus kinase (JAK) inhibitor for the treatment of rheumatoid arthritis (RA). Cytokines involved in lymphocyte development, function and homeostasis…
  • Abstract Number: 1794 • 2013 ACR/ARHP Annual Meeting

    The Jak Inihibitor Tofacitinib Suppresses Synovial Jak-Stat Signalling In Rheumatoid Arthritis

    D. L Boyle1, N. Wei2, A. K. Singhal3, D. R. Mandel4, P Mease5, A. Kavanaugh6, R. Shurmur7, J. Hodge8, Z. Luo9, S. Krishnaswami10, D. Gruben9, S. H. Zwillich9, K. Soma9, J. D. Bradley9 and G. S. Firestein11, 1Div of Rheum, UCSD School of Medicine, La Jolla, CA, 2Arthritis Treatment Center, Frederick, MD, 3Southwest Rheumatology Research LLC, Mesquite, TX, 4Office of David R Mandel MD, Inc., Mayfield Village, OH, 5Seattle Rheumatology Associates, Seattle, WA, 6UCSD School of Medicine, La Jolla, CA, 7Associated Internal Medicine Specialists, Battle Creek, MI, 8Pfizer Inc, Collegeville, PA, 9Pfizer Inc, Groton, CT, 10Clinical Pharmacology, Pfizer Inc, Groton, CT, 11Div of Rheumatology, UCSD School of Medicine, La Jolla, CA

    Background/Purpose: Tofacitinib is a novel oral Janus kinase (JAK) inhibitor for the treatment of rheumatoid arthritis (RA). The specific JAK-STAT (signal transducer and activator of…
  • Abstract Number: 1796 • 2013 ACR/ARHP Annual Meeting

    12-Week Results Of a Phase 2b Dose-Ranging Study Of Baricitinib, An Oral JAK1/ JAK2 Inhibitor In Japanese Patients With Rheumatoid Arthritis On Background Methotrexate Therapy

    Yoshiya Tanaka1, Kahaku Emoto2, Mika Tsujimoto2, Douglas E. Schlichting3 and William Macias3, 1The First Department of Internal Medicine, University of Occupational and Environmental Health, Japan, Kitakyushu, Japan, 2Eli Lilly Japan K.K., Kobe, Japan, 3Eli Lilly and Company, Indianapolis, IN

    Background/Purpose: Baricitinib (formerly LY3009104/INCB028050), a novel, oral inhibitor of JAK1 and JAK2 in the JAK-STAT signaling pathway, has been evaluated in a 12-week blinded phase…
  • Abstract Number: 1797 • 2013 ACR/ARHP Annual Meeting

    A Randomized, Dose-Ranging, Placebo-Controlled, 84-Day Study Of INCB039110, a Selective Janus Kinase-1 Inhibitor, In Patients With Active Rheumatoid Arthritis

    Monica Luchi, Rosanne Fidelus-Gort, Diane Douglas, Haifeng Zhang, Robert Flores, Robert Newton, Peggy Scherle, Swamy Yeleswaram, Xuejun Chen and Victor Sandor, Incyte Corporation, Wilmington, DE

    Background/Purpose: To characterize the safety and efficacy of INCB039110, a novel and selective JAK1 inhibitor, in patients with active RA. Methods: This phase 2, multicenter…
  • Abstract Number: 1691 • 2013 ACR/ARHP Annual Meeting

    The STAT1 Signaling Pathway In Giant Cell Arteritis

    Bjorn Hartmann1, Joyce Liao2, Michael H. Weisman3, Kenneth J. Warrington4, Jorg J. Goronzy1 and Cornelia M. Weyand5, 1Medicine: Immunology and Rheumatology, Stanford University School of Medicine, Stanford, CA, 2Byers Eye Institute at Stanford, Stanford University, Palo Alto, CA, 3Rheumatology, Cedars-Sinai Medical Center, Los Angeles, CA, 4Division of Rheumatology, Mayo Clinic, Rochester, MN, 5Medicine, Stanford University School of Medicine, Stanford, CA

    Background/Purpose: In giant cell arteritis (GCA), CD4 T cells, macrophages and multinucleated giant cells form granulomatous lesions in the walls of medium and large arteries.…
  • Abstract Number: 1433 • 2013 ACR/ARHP Annual Meeting

    Lack Of Early Clinical Response To Treatment With Baricitinib Predicts Low Probability Of Achieving Long Term DAS28-ESR Low Disease Activity Or Remission In Patients With Rheumatoid Arthritis

    Edward Keystone1, MC Genovese2, Peter Taylor3, Baojin Zhu4, Scott D. Beattie4, Stephanie de Bono4, Terence Rooney4, Douglas E. Schlichting4 and William Macias4, 1University of Toronto, Toronto, ON, Canada, 2Division of Immunology and Rheumatology, Stanford University Medical Center, Palo Alto, CA, 3NDORMS, Botnar Research Centre, University of Oxford, Oxford, United Kingdom, 4Eli Lilly and Company, Indianapolis, IN

    Background/Purpose:   Baricitinib, an oral inhibitor of JAK1 and JAK2 activity, was investigated as treatment for patients with moderately to severely active RA despite use…
  • Abstract Number: 1434 • 2013 ACR/ARHP Annual Meeting

    Assessing Janus Kinase inhibitor’s Place In Therapy In Established Rheumatoid Arthritis Patients – From a Simplified Indirect Comparison Versus Tumor Necrosis Factor Inhibitors To a Bayesian Probability Of Response – The Value Of Transparency

    Michael P. Ingham1, Paul Song2, Shannon Cartier3, Karin Lawson-Remer2 and Erin Murray2, 1Janssen Scientific Affairs, LLC, Horsham, PA, 2Doctor Evidence LLC, Santa Monica, CA, 3Optum, Eden Prairie, MN

    Background/Purpose: Bayesian style network meta-analyses and mixed treatment comparisons help address potential bias from effect modifying trial covariates within indirect comparisons and are theoretically easier…
  • Abstract Number: 822 • 2013 ACR/ARHP Annual Meeting

    Inhibition Of Casein Kinase II Reduces TGFβ Induced Fibroblast Activation and Ameliorates Experimental Fibrosis

    Yun Zhang, Internal Medicine 3, University of Erlangen-Nuremberg, Erlangen, Germany, Erlangen, Germany

    Background/Purpose: Casein kinase-2 (CK2) is a highly conserved serine/threonine kinase. CK2 is a tetramer composed of 2 catalytic subunits (α or α’) and 2 β…
  • Abstract Number: 802 • 2013 ACR/ARHP Annual Meeting

    Tofacitinib, An Oral Janus Kinase Inhibitor: Analysis Of Malignancies Across The Rheumatoid Arthritis Clinical Program

    X. Mariette1, J. R. Curtis2, E. B. Lee3, B. Benda4, I. Kaplan5, K. Soma5, R. Chew5, J. Geier6, L. Wang7 and R. Riese5, 1Paris-Sud University, Paris, France, 2Rheumatology & Immunology, University of Alabama at Birmingham, Birmingham, AL, 3Seoul National University, Seoul, South Korea, 4Pfizer Inc, Collegeville, PA, 5Pfizer Inc, Groton, CT, 6Pfizer Inc, New York, NY, 7Pfizer Worldwide R&D, Cambridge, MA

    Background/Purpose: Tofacitinib is a novel, oral Janus kinase inhibitor for the treatment of rheumatoid arthritis (RA). This analysis extended the evaluation of malignancies that occurred…
  • Abstract Number: 2374 • 2013 ACR/ARHP Annual Meeting

    Pharmacodynamics Of a Novel Jak1 Selective Inhibitor In Rat Arthritis and Anemia Models and In Healthy Human Subjects

    Jeffrey Voss1, Candace Graff2, Annette Schwartz3, Deborah Hyland4, Maria Argiriadi4, Heidi Camp5, Lori Dowding4, Michael Friedman4, Kristine Frank5, Jonathon George4, Eric Goedken4, Gloria Lo Schiavo4, Michael Morytko4, Robert o'Brien4, Robert Padley6, Matthew Rosebraugh5, Michael Rozema5, Kent Stewart5, Grier Wallace4, Neil Wishart4, Anwar Murtaza7 and Lisa Olson3, 1Immunology, AbbVie Pharmaceuticals, Worcester, MA, 2Drug Metabolism and Pharmacokinetics, Abbvie Pharmaceuticals, worcester, MA, 3AbbVie Inc, AbbVie Bioresearch Center, Worcester, MA, 4Abbvie Pharmaceuticals, worcester, MA, 5abbvie pharmaceuticals, north chicago, IL, 6AbbVie, Inc, North Chicago, IL, 7Broad Institute, Cambridge, MA

    Background/Purpose: Anti-cytokine therapies have become the mainstay of treatment for rheumatoid arthritis (RA) disease symptoms and can arrest disease progression. Despite numerous treatment options there…
  • Abstract Number: 478 • 2013 ACR/ARHP Annual Meeting

    Analysis Of The JAK1 Selectivity Of GLPG0634 and Its Main Metabolite In Different Species, Healthy Volunteers and Rheumatoid Arthritis Patients

    René Galien1, Béatrice Vayssière1, Steve de Vos2, Marielle Auberval1, Nick Vandeghinste2, Sonia Dupont1, Philippe Clément-Lacroix1, Philippe Delerive1, Frédéric Vanhoutte2, Reginald Brys2, Annegret Van der Aa2, Luc Van Rompaey2 and Gerben van 't Klooster2, 1Galapagos SASU, Romainville, France, 2Galapagos NV, Mechelen, Belgium

    Background/Purpose: The 4 Janus kinases (JAK1, JAK2, JAK3 and TYK2) are cytoplasmic tyrosine kinases that transduce intracellular signaling for cytokines including interleukins and interferons, and…
  • Abstract Number: 2381 • 2013 ACR/ARHP Annual Meeting

    The JAK1-Selective Inhibitor GLPG0634 Is Safe and Rapidly Reduces Disease Activity In Patients With Moderate To Severe Rheumatoid Arthritis; Results Of a 4-Week Dose Ranging Study

    Chantal Tasset, Pille Harrison, Annegret Van der Aa, Luc Meuleners, Frédéric Vanhoutte and Gerben van 't Klooster, Galapagos NV, Mechelen, Belgium

    Background/Purpose: GLPG0634 is an oral, selective inhibitor of Janus kinase 1 (JAK1). JAKs signal for cytokines and growth factors, including those involved in rheumatoid arthritis…
  • Abstract Number: 440 • 2013 ACR/ARHP Annual Meeting

    Cardiovascular Safety Findings In Rheumatoid Arthritis Patients Treated With Tofacitinib, A Novel, Oral Janus Kinase Inhibitor

    C. Charles-Schoeman1, P Wicker2, M. A. Gonzalez-Gay3, S. P. Wood4, M.G. Boy4, J. Geier5, D. Gruben4, K. Soma4 and R. Riese4, 1Medicine-Rheumatology, UCLA David Geffen School of Medicine, Los Angeles, CA, 2PW Consulting LLC, Mystic, CT, 3Reumatologia, Hospital Marques De Valdecilla, Santander, Spain, 4Pfizer Inc, Groton, CT, 5Pfizer Inc, New York, NY

    Background/Purpose: Tofacitinib is a novel, oral Janus kinase inhibitor for the treatment of rheumatoid arthritis (RA). Here we evaluated the cardiovascular (CV) event rates 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.).

Violation of this policy may result in the abstract being withdrawn from the meeting and other measures deemed appropriate. Authors are responsible for notifying colleagues, institutions, communications firms, and all other stakeholders related to the development or promotion of the abstract about this policy. If you have questions about the ACR abstract embargo policy, please contact ACR abstracts staff at [email protected].

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