ACR Meeting Abstracts

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Abstracts tagged "Janus kinase (JAK)"

  • Abstract Number: 1499 • 2014 ACR/ARHP Annual Meeting

    Characterization of ABT-494, a Second Generation Jak1 Selective Inhibitor

    Candace Graff1, Annette Schwartz1, Jeffrey Voss2, Neil Wishart3, Lisa Olson1, Jonathon George3, Deborah Hyland3 and Heidi Camp4, 1AbbVie Inc, AbbVie Bioresearch Center, Worcester, MA, 2Immunology, AbbVie Pharmaceuticals, Worcester, MA, 3Abbvie Pharmaceuticals, worcester, MA, 41101 Oak Street, Abbvie, Winnetka, IL

    Background/Purpose  Jak kinase blockade can effectively manage rheumatoid arthritis (RA) and in some cases achieve remission. However, first generation Jak inhibitors have not met expectations…
  • Abstract Number: 1497 • 2014 ACR/ARHP Annual Meeting

    Efficacy and Safety of Iguratimod for Rheumatoid Arthritis

    Tsuneo Kondo1, Akiko Shibata1, Ryota Sakai1, Kentaro Chino1, Ayumi Okuyama1, Hirofumi Takei1 and Koichi Amano2, 1Rheumatology and Clinical Immunology, Saitama Medical Center, Saitama Medical University, Kawagoe, Japan, 2Saitama Medical Center, Saitama Medical University, Kawagoe, Japan

    Background/Purpose: Iguratimod is a new small-molecular drug for rheumatoid arthritis (RA), which was approved on June, 2012 in Japan. The agent inhibits the production of…
  • Abstract Number: 1494 • 2014 ACR/ARHP Annual Meeting

    Treatment of Rheumatoid Arthritis Patients with the JAK1-Selective Inhibitor GLPG0634 Reverses an Arthritis-Specific Blood Gene Signature to Healthy State

    Mate Ongenaert1, Sonia Dupont2, Béatrice Vayssière2, Reginald Brys1, Luc Van Rompaey1, Christel Menet1 and René Galien2, 1Galapagos NV, Mechelen, Belgium, 2Galapagos SASU, Romainville, France

    Background/Purpose The 4 Janus kinases (JAK1, JAK2, JAK3 and TYK2) are cytoplasmic tyrosine kinases that mediate intracellular signaling of cytokines (e.g. certain interleukins and interferons)…
  • Abstract Number: 1181 • 2014 ACR/ARHP Annual Meeting

    Effects of Tofacitinib on Bone Marrow Edema, Synovitis, and Erosive Damage in Methotrexate-Naïve Patients with Early Active Rheumatoid Arthritis (Duration ≤2 Years): Results of an Exploratory Phase 2 MRI Study

    Philip G. Conaghan1, M. Østergaard2, C. Wu3, D. van der Heijde4, F. Irazoque-Palazuelos5, P. Hrycaj6, Z. Xie7, R. Zhang7, B.T. Wyman7, J.D. Bradley7, K. Soma7 and B. Wilkinson7, 1Leeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds and NIHR Leeds Musculoskeletal Biomedical Research Unit, Chapel Allerton Hospital, Leeds, United Kingdom, 2Copenhagen Center for Arthritis Research, Glostrup, Denmark, 3BioClinca Inc., Newark, CA, 4Leiden University Medical Center, Leiden, Netherlands, 5Servicio de Reumatología, Hospital Angeles Mocel, Mexico City, Mexico, 6Poznan University of Medical Sciences, Poznan, Poland, 7Pfizer Inc, Groton, CT

    Background/Purpose: Inflammation of the synovium and in particular the bone marrow, as assessed by magnetic resonance imaging (MRI), have been identified as prognostic indicators of…
  • Abstract Number: 849 • 2014 ACR/ARHP Annual Meeting

    Tofacitinib, an Oral Janus Kinase Inhibitor, in the Treatment of Rheumatoid Arthritis: Safety and Efficacy in Open-Label, Long-Term Extension up to 6 Years

    J. Wollenhaupt1, J. Silverfield2, E.B. Lee3, S.P. Wood4, K. Terry4, H. Nakamura5, K. Kwok6, A. Anisfeld6, C. Nduaka4, R. Riese4 and L. Wang4, 1Schoen-Klinik Hamburg-Eilbek Teaching Hospital of the University of Hamburg, Hamburg, Germany, 2Healthpoint Medical Group, Tampa, FL, 3Seoul National University, Seoul, South Korea, 4Pfizer Inc, Groton, CT, 5Pfizer Inc, Tokyo, Japan, 6Pfizer Inc, New York, NY

    Background/Purpose: Tofacitinib is an oral Janus kinase inhibitor for the treatment of rheumatoid arthritis (RA). Here we report tofacitinib safety, tolerability, and durability of response…
  • Abstract Number: 461 • 2014 ACR/ARHP Annual Meeting

    Comprehensive Summary of the Efficacy and Safety of Tofacitinib 5mg Twice Daily in Patients with Rheumatoid Arthritis and an Inadequate Response to Disease-Modifying Antirheumatic Drugs

    P. Bird1, W. Bensen2, B. El-Zorkany3, J. Kaine4, B.H. Manapat-Reyes5, V. Pascual-Ramos6, D. Witcombe7, A. Anisfeld8, K. Soma9, R. Zhang9 and K. Thirunavukkarasu7, 1Combined Rheumatology Practice, Sydney, Australia, 2St. Joseph's Healthcare, McMaster University, Hamilton, ON, Canada, 3Department of Rheumatology, Cairo University, Cairo, Egypt, 4Sarasota Arthritis Research Center, Sarasota, FL, 5Section of Rheumatology, Department of Medicine, University of the Philippines - Philippine General Hospital, Manila, Philippines, 6Department of Immunology and Rheumatology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Mexico, 7Pfizer Australia, Sydney, Australia, 8Pfizer Inc, New York, NY, 9Pfizer Inc, Groton, CT

    Background/Purpose: Tofacitinib has been approved in the US and other countries at the recommended dose 5 mg BID in patients (pts) with rheumatoid arthritis (RA) and…
  • Abstract Number: 460 • 2014 ACR/ARHP Annual Meeting

    Analysis of Non-Melanoma Skin Cancer Across the Tofacitinib Rheumatoid Arthritis Clinical Program

    Jeffrey R. Curtis1, E.B. Lee2, G. Martin3, X. Mariette4, K.K. Terry5, Y. Chen6, J. Geier7, J. Andrews5, M. Kaur6, K. Kwok7 and C. Nduaka5, 1University of Alabama at Birmingham, Birmingham, AL, 2Seoul National University College of Medicine, Seoul, South Korea, 3Dermatology and Laser Center of Maui, Kihei, HI, 4Paris-Sud University, Paris, France, 5Pfizer Inc, Groton, CT, 6Pfizer Inc, Collegeville, PA, 7Pfizer Inc, New York, NY

    Background/Purpose: Tofacitinib is an oral Janus kinase inhibitor for the treatment of rheumatoid arthritis (RA). The incidence of non-melanoma skin cancer (NMSC) in the tofacitinib…
  • Abstract Number: 465 • 2014 ACR/ARHP Annual Meeting

    18-Month Worldwide Post-Marketing Surveillance Experience of Tofacitinib

    S. Cohen1, Jeffrey R. Curtis2, Roy Fleischmann1 and Y. Chen3, 1Metroplex Clinical Research Center, Dallas, TX, 2University of Alabama, Birmingham, AL, 3Pfizer Inc, Collegeville, PA

    Background/Purpose: Post-marketing surveillance is an important part of monitoring adverse events (AEs) following the approval of new drugs. Tofacitinib is an oral Janus kinase inhibitor…
  • Abstract Number: 2822 • 2014 ACR/ARHP Annual Meeting

    Safety and Efficacy of Baricitinib through 128 Weeks in an Open-Label, Long-Term Extension Study in Patients with Rheumatoid Arthritis

    Edward C. Keystone1, Peter C. Taylor2, Mark C Genovese3, Douglas E. Schlichting4, Inmaculada De La Torre5, Scott D. Beattie4 and Terence Rooney4, 1University of Toronto, Mount Sinai Hospital, Toronto, ON, Canada, 2NDORMS, Botnar Research Centre, University of Oxford, Oxford, United Kingdom, 3Division of Immunology and Rheumatology, Stanford University Medical Center, Palo Alto, CA, 4Eli Lilly and Company, Indianapolis, IN, 5AVDA. DE LA INDUSTRIA 30, Eli Lilly and Company, Alcobendas, Spain

    Background/Purpose: Baricitinib is an oral inhibitor of JAK1/JAK2 being investigated as a treatment for rheumatoid arthritis (RA).  In a phase 2b study, baricitinib treatment resulted…
  • Abstract Number: 39 • 2014 ACR/ARHP Annual Meeting

    Human CD14+ Monocytes Stimulated with a Combination of TNFα and IL-6 Differentiate into Osteoclast-like Cells with Bone-Resorption Activity

    Kazuhiro Yokota1, Kojiro Sato2, Yoshimi Aizaki2, Yuji Akiyama2 and Toshihide Mimura2, 1Department of Rheumatology & Applied Immunology, Faculty of Medicine, Saitama Medical University, Saitama, Japan, 2Department of Rheumatology and Applied Immunology, Faculty of Medicine, Saitama Medical University, Saitama, Japan

    Background/Purpose Proinflammatory cytokines play an important role in bone destruction in rheumatoid arthritis (RA), as inferred by the efficacy of biologics. Previously, we reported that…
  • 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.…
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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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