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

  • Abstract Number: 2547 • 2015 ACR/ARHP Annual Meeting

    NIP-565, a Novel JAK1-Selective Inhibitor, for the Treatment of Rheumatoid Arthritis

    Yuuki Hidaka1, Takanori Nakamura2, Tadashi Igarashi2, Takeshi Nanya2, Shuhei Hagiwara2, Kazuya Takeuchi2, Tomonori Yaguchi3, Yutaka Kawakami3 and Takeshi Naito2, 1Pharmaceutical Research Department, Nissan Chemical Industries,LTD., Saitama, Japan, 2Nissan Chemical Industries,LTD., Saitama, Japan, 3Keio University School of Medicine, Tokyo, Japan

    Background/Purpose: Non-selective Janus kinase (JAK) inhibitors have shown long-term efficacy in treating rheumatoid arthritis (RA). However, clinical efficacy is limited due to concerns of dose-limiting…
  • Abstract Number: 2487 • 2012 ACR/ARHP Annual Meeting

    24-Week Results of a Blinded Phase 2b Dose-Ranging Study of Baricitinib, an Oral Janus Kinase 1/ Januse Kinase 2 Inhibitor, in Combination with Traditional Disease Modifying Antirheumatic Drugs in Patients with Rheumatoid Arthritis

    Mark C. Genovese1, Edward Keystone2, Peter Taylor3, Edit Drescher4, Pierre-Yves Berclaz5, Chin H. Lee5, Douglas E. Schlichting5, Scott D. Beattie5, Rosanne K. Fidelus-Gort6, Monica E. Luchi6 and William Macias5, 1Division of Rheumatology, Stanford University, Palo Alto, CA, 2University of Toronto, Toronto, ON, Canada, 3NDORMS, Botnar Research Centre, University of Oxford, Oxford, United Kingdom, 4Internal Medicine and Rheumatology, Veszprém Csolnoky Ferenc County Hospital, Department of Rheumatology and Physical Rehabilitation, Veszprém, Hungary, 5Eli Lilly and Company, Indianapolis, IN, 6E361/309, Incyte Corporation, Wilmington, DE

    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 24 week blinded…
  • Abstract Number: 1331 • 2012 ACR/ARHP Annual Meeting

    Once Daily High Dose Regimens of GLPG0634 in Healthy Volunteers Are Safe and Provide Continuous Inhibition of JAK1 but Not JAK2

    Florence Namour1, René Galien1, Lien Gheyle2, Frédéric Vanhoutte3, Béatrice Vayssière1, Annegret Van der Aa3, Bart Smets3 and Gerben van 't Klooster3, 1Galapagos SASU, Romainville, France, 2SGS Clinical Pharmacology Unit, Antwerp, Belgium, 3Galapagos NV, Mechelen, Belgium

    Background/Purpose: GLPG0634 is an orally-available, selective inhibitor of Janus kinase 1 (JAK1) with an IC50 of 0.6 μM and a 30-fold selectivity over JAK2 in…
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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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