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  • Abstract Number: 1638 • 2015 ACR/ARHP Annual Meeting

    Early Response As a Predictor of Long-Term Remission in DMARD-Naïve Patients with Severe, Active and Progressive Rheumatoid Arthritis Treated with Certolizumab Pegol in Combination with Methotrexate

    Michael Weinblatt1, Clifton Bingham2, Gerd Burmester3, VP Bykerk4, Daniel E. Furst5, Xavier Mariette6, Désirée van der Heijde7, Daljit Tatla8, Catherine Arendt9, Irina Mountian10, Brenda VanLunen11 and Paul Emery12, 1Rheumatology Immunology & Allergy, Brigham and Women's Hospital, Boston, MA, 2Johns Hopkins University, Baltimore, MD, 3Department of Rheumatology and Clinical Immunology, Charité - Universitätsmedizin Berlin, Berlin, Germany, 4Hospital for Special Surgery, New York, NY, 5Medicine, University of California, Los Angeles, David Geffen School of Medicine, Los Angeles, CA, 6Université Paris-Sud, AP-HP, Hôpitaux Universitaires Paris-Sud, Paris, France, 7University Hospital, Maastricht, Netherlands, 88010 Arco Corporate Dr, UCB Pharma, Raleigh, NC, 9Global Medical Affairs, UCB Pharma, Brussels, Belgium, 10UCB Pharma, Brussels, Belgium, 11UCB Pharma, Raleigh, NC, 12Leeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds, Leeds, United Kingdom

    Background/Purpose: In established rheumatoid arthritis (RA), a lack of response to treatment with certolizumab pegol (CZP) at early timepoints is associated with a low probability…
  • Abstract Number: 1639 • 2015 ACR/ARHP Annual Meeting

    Clinical Outcomes for Rheumatoid Arthritis Patients Receiving Tofacitinib Monotherapy in the Open-Label Long-Term Extension over 6 Years

    Roy Fleischmann1, Yusuf Yazici2, Jürgen Wollenhaupt3, Lisy Wang4, Anna Maniccia5, Kenneth Kwok4, Liza Takiya5 and Ronald van Vollenhoven6, 1Rheumatology, Metroplex Clinical Research Center, Dallas, TX, 2New York University Hospital for Joint Diseases, New York, NY, 3Teaching Hospital of the University of Hamburg, Schoen-Klinik Hamburg-Eilbek, Hamburg, Germany, 4Pfizer Inc, Groton, CT, 5Pfizer Inc, New York, NY, 6The Karolinska Institute, Stockholm, Sweden

    Background/Purpose: Treatment options delivering sustained efficacy when given as monotherapy in RA are limited.1 Tofacitinib is an oral Janus kinase inhibitor for the treatment of…
  • Abstract Number: 1640 • 2015 ACR/ARHP Annual Meeting

    Effect of Methotrexate Dose on the Efficacy of Tofacitinib: Treatment Outcomes from a Phase 3 Clinical Trial of Patients with Rheumatoid Arthritis

    Roy Fleischmann1, Philip J. Mease2, Sergio Schwartzman3, Lie-Ju Hwang4, Aditya Patel5, Koshika Soma4, Carol A. Connell6, Liza Takiya4 and Eustratios Bananis7, 1Rheumatology, Metroplex Clinical Research Center, Dallas, TX, 2Rheumatology Research, Swedish Medical Center, Seattle, WA, 3Hospital for Special Surgery, New York, NY, 4Pfizer Inc, New York, NY, 5Inventiv Health Inc, South Plainfield, NJ, 6Pfizer Inc, Groton, CT, 7Pfizer Inc, Collegeville, PA

    Background/Purpose: Tofacitinib is an oral Janus kinase inhibitor for the treatment of rheumatoid arthritis (RA). ORAL Scan was a 2-year, randomized, Phase 3, clinical trial…
  • Abstract Number: 1641 • 2015 ACR/ARHP Annual Meeting

    B Cell Depletion with Rituximab in Patients with Rheumatoid Arthritis: Multiplex Bead Array Reveals Kinetics of IgG and IgA Autoantibodies to Citrullinated Antigens

    Geraldine Cambridge1, Lauren J. Lahey2, Maria J. Leandro1, William H. Robinson3 and Jeremy Sokolove4, 1Rheumatology, University College London, London, United Kingdom, 2Medicine, VA Palo Alto HealthCare System and Stanford University, Palo Alto, CA, 3VA Palo Alto Health Care System and Stanford University, Palo Alto, CA, 4Medicine, VA Palo Alto Health Care System and Stanford University, Palo Alto, CA

    Background/Purpose: Seropositivity for rheumatoid factors and anti-citrullinated (Cit) protein antibodies (ACPA) are the strongest predictor for clinical response to rituximab (RTX) in rheumatoid arthritis (RA).…
  • Abstract Number: 1642 • 2015 ACR/ARHP Annual Meeting

    A Systematic Review and Network Meta-Analysis on the Efficacy of Tumor Necrosis Factor Inhibitor-Methotrexate Combination Therapy Versus Triple Therapy in Methotrexate Inadequate Responders with Rheumatoid Arthritis

    Roy Fleischmann1, Janet E. Pope2, Vanita Tongbram3, Derek Tang4, James Chung5, David Collier5, Shilpa Urs3, Kerigo Ndirangu3, George A. Wells6 and Ronald F. van Vollenhoven7, 1Rheumatology, Metroplex Clinical Research Center, Dallas, TX, 2University of Western Ontario, London, ON, Canada, 3ICON Plc., Morristown, NJ, 4Amgen, Inc., Thousand Oaks, CA, 5Amgen Inc., Thousand Oaks, CA, 6Cardiovascular Research Reference Centre, University of Ottawa Heart Institute, Ottawa, ON, Canada, 7Department of Medicine, Unit for Clinical Therapy Research, Inflammatory Diseases (ClinTRID), The Karolinska Institute, Stockholm, Sweden

    Background/Purpose: Previously published rheumatoid arthritis (RA) trials in which TNFi-MTX and triple therapy (MTX + hydroxychloroquine + sulfasalazine) were included as treatment arms in MTX…
  • Abstract Number: 1643 • 2015 ACR/ARHP Annual Meeting

    Modified-Release Formulation of Tofacitinib: Evaluation of Pharmacokinetics Compared with Immediate-Release Tofacitinib and Impact of Food

    Manisha Lamba1, Rong Wang1, Tracey Fletcher2, Christine Alvey1, Joseph Kushner1 and Thomas Stock2, 1Pfizer Inc, Groton, CT, 2Pfizer Inc, Collegeville, PA

    Background/Purpose: Tofacitinib is an oral Janus kinase inhibitor for the treatment of RA. A modified-release (MR) formulation has been designed to enable once daily (QD)…
  • Abstract Number: 1644 • 2015 ACR/ARHP Annual Meeting

    Routine Assessment of Patient Index Data 3 (RAPID3)-Defined Remission Is As Stringent As ACR/EULAR Boolean-Defined Remission in a Clinical Trial of Patients with Early Rheumatoid Arthritis Treated with Abatacept

    Yusuf Yazici1, KK Gandhi2, E Alemao2 and Daniel E. Furst3, 1NYU Hospital for Joint Diseases, New York, NY, 2Bristol-Myers Squibb, Princeton, NJ, 3Medicine, University of California, Los Angeles, David Geffen School of Medicine, Los Angeles, CA

    Background/Purpose: Routine Assessment of Patient Index Data 3 (RAPID3) comprises the three patient-reported ACR RA Core Data Set measures: function (HAQ-DI), pain and patient global…
  • Abstract Number: 1645 • 2015 ACR/ARHP Annual Meeting

    Tofacitinib, an Oral Janus Kinase Inhibitor, in the Treatment of Rheumatoid Arthritis: Safety and Clinical and Radiographic Efficacy in Open-Label, Long-Term Extension Studies over 7 Years

    Jürgen Wollenhaupt1, Joel Silverfield2, Eun Bong Lee3, Ketti Terry4, Kenneth Kwok5, Irina Lazariciu6, Chudy Nduaka7, Carol A. Connell4, Ryan DeMasi5 and Lisy 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, New York, NY, 6Quintiles, Saint-Laurent, QC, Canada, 7Pfizer Inc, Collegeville, PA

    Background/Purpose: Tofacitinib is an oral Janus kinase inhibitor for the treatment of rheumatoid arthritis (RA). We report tofacitinib safety, tolerability, and clinical response over 84 months…
  • Abstract Number: 1646 • 2015 ACR/ARHP Annual Meeting

    Which Factors Influence the Prescription of Tocilizumab Alone or in Combination with Dmards in Rheumatoid Arthritis Patients in a Real Life Setting? the ACT-Solo Study: An Analysis of Efficacy and Safety at 12 Months

    Jacques Tebib1, Isabelle Idier2, Mathieu Coudert3, David Pau4, Jean-Francis Maillefert5 and Rene-Marc Flipo6, 1Rheumatology, Hospices Civils de Lyon, Centre Hospitalier Lyon-Sud, Pierre-Bénite, France, 2Chugai Pharma, La Defense, France, 3Statistics, Experis IT, Nanterre, France, 4Statistics, Roche, Boulogne-Billancourt, France, 5Rheumatology, University Hospital, Dijon, France, 6Rheumatology, University Hospital, Lille, France

    Background/Purpose: Baseline factors influencing the use of tocilizumab (TCZ) in monotherapy (Mono) instead of combination with DMARDs (Combo) in real-life practice in RA patients (pts)…
  • Abstract Number: 1647 • 2015 ACR/ARHP Annual Meeting

    A Randomized, Clinical Trial to Assess the Relative Efficacy and Tolerability of Two Doses of Etoricoxib in Patients with Rheumatoid Arthritis

    Kara Bickham1, Désirée van der Heijde2, Narinder Rawal3, Joachim Sieper4, Boyd Scott5, Nancy Frontera1, Sandhya Shah1, Paul Stryszak1, Dimitris Papanicolaou1, Zoran Popmihajlov1 and Paul Peloso1, 1Merck & Co., Inc., Kenilworth, NJ, 2University Hospital, Maastricht, Netherlands, 3Orebro University Hospital, Orebro, Sweden, 4Rheumatology, Charite - Campus Benjamin Franklin, Berlin, Germany, 5Merck Sharp & Dohme Corp., Whitehouse Station, NJ

    Background/Purpose: Etoricoxib, a selective cyclooxygenase-2 (COX-2) inhibitor, provides symptom modification in RA patients. Previous dose-ranging studies in RA demonstrated the clinical efficacy of etoricoxib 90…
  • Abstract Number: 1648 • 2015 ACR/ARHP Annual Meeting

    The Balance of Foxp3/Ror-Gammat Expression Is Altered By Tocilizumab and By Abatacept in Patients with Rheumatoid Arthritis

    Yoshifumi Tada1, Syuichi Koarada2, Nobuyuki Ono2, Akihito Maruyama2, Satoko Tashiro2, Yukiko Tokuda2, Yukihide Ono2, Yoshinobu Nakao2 and Akihide Ohta3, 1Department of Internal Medicine, Division of Rheumatology, Saga University, Saga, Japan, 2Rheumatology, Saga University, Saga, Japan, 3Department of Adult and Gerontological Nursing, Saga University School of Medicine, Saga, Japan

    Background/Purpose: It has been shown that the balance between Th17 cells and regulatory T (Treg) cells plays an important role for the development of autoimmune…
  • Abstract Number: 1649 • 2015 ACR/ARHP Annual Meeting

    Long-Term Safety and Efficacy of Olokizumab in Patients with Moderate-to-Severe Rheumatoid Arthritis Who Have Previously Failed Anti-TNF Treatment

    Mark C. Genovese1, Roy Fleischmann2, Yoshiya Tanaka3, Daniel E. Furst4, Hisashi Yamanaka5, Rajesh Joshi6, Wei Zhu7, Jing Shao8, Hideki Mashimo8 and Tsutomu Takeuchi9, 1Division of Rheumatology, Stanford University Medical Center, Palo Alto, CA, 2Metroplex Clinical Research Center, University of Texas Southwestern Medical Center, Department of Medicine, Dallas, TX, 3The First Department of Internal Medicine, University of Occupational and Environmental Health, Kitakyushu, Japan, 4Medicine, University of California, Los Angeles, David Geffen School of Medicine, Los Angeles, CA, 5Institute of Rheumatology, Tokyo Women's Medical University, Tokyo, Japan, 6Quintiles Inc., Mumbai, India, 7UCB Pharma, Raleigh, NC, 8UCB Pharma, Tokyo, Japan, 9Keio University School of Medicine, Tokyo, Japan

    Background/Purpose: Olokizumab (OKZ) is a humanized anti-interleukin-6 monoclonal antibody in development for moderate-to-severe rheumatoid arthritis (RA) treatment. OKZ efficacy and safety were assessed in the…
  • Abstract Number: 1650 • 2015 ACR/ARHP Annual Meeting

    Tocilizumab Monotherapy in Early Rheumatoid Arthritis: Data from Two Phase 3 Randomized Controlled Trials

    Gerd Burmester1, Attila Pethö-Schramm2, Caroline Keane3 and Graeme Jones4, 1Department of Rheumatology and Clinical Immunology, Charité - Universitätsmedizin Berlin, Berlin, Germany, 2F. Hoffmann-La Roche, Basel, Switzerland, 3Roche Products Ltd., Welwyn Garden City, United Kingdom, 4Menzies Institute for Medical Research, University of Tasmania, Hobart, Australia

    Background/Purpose: Disease remission is the current treatment goal for patients (pts) with early RA (eRA). Initiation of an anti-TNF agent ± methotrexate (MTX) is recommended…
  • Abstract Number: 1651 • 2015 ACR/ARHP Annual Meeting

    Comparison of Oral Glucocorticoid (OGC)-Sparing Effects in Tocilizumab and Other Biologic Dmards Using Multilevel Models in an Administrative Health Care Claims Database

    Brandon Arnieri1, Khaled Sarsour1, David Oliveri1, Attila Pethö-Schramm2, Avani Shah1 and George Quartey1, 1Genentech, South San Francisco, CA, 2F. Hoffmann-La Roche, Basel, Switzerland

    Background/Purpose : The current treatment paradigm in rheumatoid arthritis (RA) is to attempt to decrease, when clinically feasible, concomitant use of OGCs after their use…
  • Abstract Number: 1652 • 2015 ACR/ARHP Annual Meeting

    A HPLC-SRM-MS Based Method for the Detection of Adherence to Low-Dose Oral Methotrexate

    James Bluett1, Thierry Wendling2, Kayode Ogungbenro2, Isabel Riba-Garcia3, Richard Unwin3, Suzanne M. Verstappen4 and Anne Barton5,6, 1Arthritis Research UK Centre for Genetics and Genomics, The University of Manchester, Manchester, United Kingdom, 2Centre for Applied Pharmacokinetic Research, Manchester Pharmacy School, The University of Manchester, Manchester, United Kingdom, 3Centre for Advanced Discovery and Experimental Therapeutics (CADET), Central Manchester University Hospitals NHS Foundation Trust, Manchester Academic Health Sciences Centre, Manchester, United Kingdom, 4Arthritis Research UK Centre for Epidemiology, The University of Manchester, Manchester, United Kingdom, 5Arthritis Research UK Centre for Genetics and Genomics, University of Manchester, Manchester, United Kingdom, 6NIHR Manchester Musculoskeletal Biomedical Research Unit, Central Manchester Foundation Trust and University of Manchester, Manchester Academy of Health Sciences, Manchester, United Kingdom

    Background/Purpose: Whilst methotrexate (MTX) is the first-line treatment of rheumatoid arthritis (RA), response is not universal. Rates of adherence reported in the literature range from…
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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 CT on October 25. 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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