ACR Meeting Abstracts

ACR Meeting Abstracts

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Abstracts tagged "inflammation and psoriasis"

  • Abstract Number: 15L • 2016 ACR/ARHP Annual Meeting

    Selective Oral ROCK2 Inhibitor Reduces Clinical Scores in Patients with Psoriasis vulgaris and Normalizes Skin Pathology Via Concurrent Regulation of IL-17 and IL-10 Levels

    Alexandra Zanin-Zhorov1, Jonathan Weiss1, Alissa Trzeciak1, Carmen Arencibia1, Seetharam Polimera1, Wei Chen1, Jingya Zhang1, Melanie Nyuydzefe1, Judilyn Fuentes-Duculan2, Kathleen Bonifacio2, Norma Kunjravia2, Inna Cueto2, Mark Berger1, James Krueger2, Samuel Waksal1 and John Ryan1, 1Kadmon, New York, NY, 2Rockefeller University, New York, NY

    Background/Purpose: Rho-associated kinase 2 (ROCK2) was shown to be implicated in regulation of autoimmunity in mice and humans1. Previous findings demonstrated that oral administration of…
  • Abstract Number: 2704 • 2016 ACR/ARHP Annual Meeting

    Discovery of a Small Molecule Inhibitor of the Wnt Pathway (SM04755) As a Potential Topical Treatment for Psoriasis

    Vishal Deshmukh1, Melinda Pedraza1, Maureen Ibanez1, Luis Dellamary1, Josh Stewart1, Timothy Seo1, Benoit Melchior1, John Hood2 and Yusuf Yazici1, 1Samumed, LLC, San Diego, CA, 2Samumed, LLC (formerly), San Diego, CA

    Background/Purpose: Psoriasis is an auto-immune disease of the skin, characterized by inflammation and fibrosis producing patches of red, itchy and scaly skin. Wnt signaling plays…
  • Abstract Number: 2934 • 2016 ACR/ARHP Annual Meeting

    Clinical Assessment of the Monoclonal Anitbody, PRX003, a Potential Novel Treatment for Th17-Mediated Inflammatory Disease

    Gene G. Kinney1, Kenneth Flanagan1, Michael Skov1, Ronald Goldblum2, Sue Griffith3, Robin M. Barbour1, Wagner Zago1, Ted Yednock1, Martin Koller1 and Dan Ness1, 1Prothena Biosciences Inc, South San Francisco, CA, 2Carlsbad Pharmaceutical Consulting, Inc., Carlsbad, CA, 3ClinPharma Services, Inc, San Diego, CA

    Background/Purpose: Melanoma cell adhesion molecule (MCAM; CD146) is expressed on the surface of Th17 cells, which have the capacity to produce IL-17 and a multitude…
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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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