ACR Meeting Abstracts

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Abstracts tagged "Remission and tofacitinib"

  • Abstract Number: 1475 • 2019 ACR/ARP Annual Meeting

    Comparison of Different Remission Indices in Patients with Psoriatic Arthritis: A Post Hoc Analysis of Data from Phase 3 Tofacitinib Studies

    Gustavo Citera1, Emilce Schneeberger 2, Peter Nash 3, Josef Smolen 4, Philip Mease 5, Enrique Soriano 6, Vesna Matulic 7, Claudia Helling 8, Annette Szumski 9, Rajiv Mundayat 10, Daniela Graham 11 and Dario Ponce de Leon 12, 1Instituto de Rehabilitación Psicofísica, Ciudad Autónoma de Buenos Aires, Buenos Aires, Argentina, 2Instituto de Rehabilitación Psicofísica, Buenos Aires, Argentina, 3University of Queensland, Brisbane, Queensland, Australia, 4Medical University of Vienna, Vienna, Austria, 5Swedish Medical Center/Providence St Joseph Health, and University of Washington, Seattle, WA, 6Rheumatology Section, Internal Medicine Service, Hospital Italiano de Buenos Aires, Argentina., Buenos Aires, Buenos Aires, Argentina, 7Pfizer Chile S.A., Santiago, Chile, 8Pfizer Inc, Buenos Aires, Argentina, 9Syneos Health, Princeton, NJ, 10Pfizer Inc, New York, NY, 11Pfizer Inc, Groton, CT, 12Pfizer Inc, Lima, Peru

    Background/Purpose: An international task force has agreed that remission or low disease activity (LDA) are key treatment targets for patients (pts) with PsA, and recommends…
  • Abstract Number: 1600 • 2016 ACR/ARHP Annual Meeting

    Evaluation of Disease Activity in Patients with Rheumatoid Arthritis Treated with Tofacitinib By RAPID3: An Analysis of Data from 6 Phase 3 Studies

    Martin J Bergman1, Yusuf Yazici2, Ara Dikranian3, Jeffrey Bourret4, Chuanbo Zang5, Christopher F Mojcik6 and Eustratios Bananis5, 1Drexel University College of Medicine, Philadelphia, PA, 2New York University Division of Rheumatology, New York, NY, 3San Diego Arthritis Medical Clinic, San Diego, CA, 4Pfizer, Inc., Collegeville, PA, 5Pfizer Inc, Collegeville, PA, 6Pfizer Inc, New York, NY

    Background/Purpose: Tofacitinib is an oral Janus kinase inhibitor for the treatment of RA. The treatment target for RA is remission or low disease activity (LDA).…
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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.).

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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