ACR Meeting Abstracts

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Abstracts tagged "Biologics and psoriatic arthritis"

  • Abstract Number: 807 • 2019 ACR/ARP Annual Meeting

    Guselkumab, an Anti-interleukin-23p19 Monoclonal Antibody, in Patients with Active Psoriatic Arthritis Who Were Biologic-Naïve or Prior TNFα Inhibitor-Treated: Week 24 Results of a Phase 3, Randomized, Double-blind, Placebo-controlled Study

    Atul Deodhar1, Philip Helliwell 2, Wolf-Henning Boencke 3, Elizabeth Hsia 4, Alexa Kollmeier 5, Ramanand Subramanian 5, Xie Xu 5, Shihong Sheng 5, Bei Zhou 5 and Christopher Ritchlin 6, 1Oregon Health & Science University, Portland, OR, 2University of Leeds, Leeds, United Kingdom, 3Geneva Univ Hospitals, Geneva, Switzerland, 4Janssen Research & Development, LLC/University of Pennsylvania, Spring House/Philadelphia, PA, 5Janssen Research & Development, LLC, Spring House, PA, 6Division of Allergy, Immunology and Rheumatology, Center for Musculoskeletal Research, University of Rochester School of Medicine and Dentistry, Rochester, NY, USA, Rochester, NY

    Background/Purpose: Guselkumab (GUS), an anti-interleukin-23p19 monoclonal antibody, is approved to treat PsO. We evaluated GUS efficacy and safety in a Phase 3, double-blind, PBO-controlled trial…
  • Abstract Number: 2846 • 2015 ACR/ARHP Annual Meeting

    Modifications to Biologic Therapy and Economic Implications in Psoriatic Arthritis Patients

    Jacqueline B. Palmer, Yunfeng Li, Vivian Herrera, Minlei Liao and Zafer Ozturk, Novartis Pharmaceuticals Corporation, East Hanover, NJ

    Background/Purpose: Limited information exists on the long term real-world treatment patterns of biologics for psoriatic arthritis (PsA) in the US population. We assessed medication persistence…
  • Abstract Number: 539 • 2014 ACR/ARHP Annual Meeting

    Efficacy and Safety of Ustekinumab in Psoriatic Arthritis Patients with Spondylitis and Peripheral Joint Involvement: Results from a Phase 3, Multicenter, Double-Blind, Placebo-Controlled Study

    Arthur Kavanaugh1, Lluís Puig Sanz2, Alice B. Gottlieb3, Christopher T. Ritchlin4, Yin You5, Yuhua Wang5, Alan M. Mendelsohn6, Michael Song5, Proton Rahman7 and Iain B. McInnes8, 1University of California San Diego, La Jolla, CA, 2Dermatology Department, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain, 3Tufts Medical Center, Boston, MA, 4Allergy Immunology & Rheumatology, University of Rochester Medical Center, Rochester, NY, 5Janssen Research & Development, LLC., Spring House, PA, 6Immunology, Janssen Research & Development, LLC., Spring House, PA, 7Faculty of Medicine, Memorial University of Newfoundland, St. John's, NF, Canada, 8University of Glasgow, Glasgow, United Kingdom

     Background/Purpose: IL-23 may be implicated in spondylitis. A substantial number of pts with spondylitis and peripheral joint involvement were enrolled in PSUMMIT. We evaluated the…
  • Abstract Number: 302 • 2013 ACR/ARHP Annual Meeting

    Maintenance Of Efficacy and Safety Of Ustekinumab In Patients With Active Psoriatic Arthritis Despite Prior Conventional Nonbiologic and Anti-TNF Biologic Therapy:  1‑year Results Of a Phase 3, Multicenter, Double-Blind, Placebo-Controlled Trial

    Christopher T. Ritchlin1, Iain B. McInnes2, Arthur Kavanaugh3, Lluis Puig4, Proton Rahman5, Carrie Brodmerkel6, Shu Li6, Yaung-Kaung Shen6, Mittie K. Doyle6, Alan M. Mendelsohn7 and Alice B. Gottlieb8, 1Allergy, Immunology and Rheumatology, University of Rochester, Rochester, NY, 2Institute of Infection, Immunity and Inflammation, University of Glasgow, Glasgow, United Kingdom, 3University of California, San Diego, La Jolla, CA, 4Universitat Autònoma de Barcelona, Barcelona, Spain, 5Faculty of Medicine, Memorial University of Newfoundland, St. John's, NF, Canada, 6Janssen Research & Development, LLC., Spring House, PA, 7Immunology, Janssen Research & Development, LLC., Spring House, PA, 8Tufts Medical Center, Boston, MA

    Background/Purpose: Ustekinumab (UST) has demonstrated substantial efficacy and an acceptable safety profile, and is approved for use, in treating moderate-to-severe psoriasis. UST has also demonstrated…
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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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