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Abstracts tagged "treatment"

  • Abstract Number: 1665 • 2015 ACR/ARHP Annual Meeting

    Treatment Patterns in Rheumatoid Arthritis after Methotrexate: Data from a Rheumatoid Arthritis Cohort

    Janet E. Pope1, Mohammad Movahedi2,3, Angela Cesta2, Xiuying Li2, Sandra Couto2, Emmanouil Rampakakis3, John S. Sampalis3,4, Claire Bombardier2,5,6 and OBRI Investigators, 1University of Western Ontario, London, ON, Canada, 2Toronto General Hospital Research Institute, University Health Network, Toronto, ON, Canada, 3JSS Medical Research, St-Laurent, QC, Canada, 4McGill University, Montreal, QC, Canada, 5University of Toronto, Department of Medicine (DOM) and Institute of Health Policy Management, and Evaluation (IHPME), Toronto, ON, Canada, 6Division of Rheumatology, Mount Sinai Hospital, Toronto, ON, Canada

    Background/Purpose: Guidelines support the use of combination conventional synthetic Disease-Modifying Antirheumatic Drugs (csDMARDs), switching csDMARDs and/or use of biologic DMARDs (bDMARDs) treatment in active rheumatoid…
  • Abstract Number: 2138 • 2015 ACR/ARHP Annual Meeting

    Safety and Efficacy Results of a Phase 2, Double-Blind, Placebo-Controlled Clinical Study of Duvelisib with Background Methotrexate (MTX) in Adults with Moderate-to-Severe Rheumatoid Arthritis (RA)

    Richard Leff1, Sunil Kumar2, Natalia Nikulenkova3, Igor Kaidashev4, Kerstin Allen5, Joi Dunbar6, Howard Stern7, Julian Adams6 and Michael Weinblatt8, 1Clinical Research, Infinity Pharmaceuticals, Inc., Cambridge, MA, 2Centre for Clinical Research and Effective Practice (CCRep), Auckland, New Zealand, 3State Budgetary Healthcare Institution of Vladimir Region, Regional Clinical Hospital, Vladimir, Russia, 4City Clinical Hospital #1 of Poltava City, Poltava, Ukraine, 5Biostatistics, Infinity Pharmaceuticals, Inc., Cambridge, MA, 6Infinity Pharmaceuticals, Inc., Cambridge, MA, 7Translational Science, Infinity Pharmaceuticals, Inc., Cambridge, MA, 8Division of Rheumatology, Immunology and Allergy, Brigham and Women's Hospital, Boston, MA

    Background/Purpose:  Duvelisib is a potent, oral, dual inhibitor of phosphoinositide-3-kinase (PI3K)-δ,γ being developed for hematologic malignancies, and was also explored in early phase studies in…
  • Abstract Number: 2493 • 2015 ACR/ARHP Annual Meeting

    Improvement of Disease Activity and Quality of Care in a Cohort of Rheumatoid Arthritis Patients Treated with Conventional Dmard Therapy Under Treat to Target Recommendations and a Model of Patient-Centered Care

    Pedro Ivan Santos-Moreno1, Ginna Saavedra2, Rosana Ramirez2, Laura Villarreal2, Ana Bolena Cardozo2, Vanessa Giraldo2, Paola Martinez2, Adriana Sanchez2, Merle Sanchez2, Danny Gomez2 and Juan Manuel Bello2, 1Rheumatology, Biomab, Center for Rheumatoid Arthritis., Bogota, Colombia, 2Rheumatology, Biomab, Center for Rheumatoid Arthritis, Bogota, Colombia, Bogota, Colombia

    Background/Purpose: Treat to Target (T2T) strategy becomes from the need to develop therapeutic targets and tools to achieve defined outcomes in rheumatoid arthritis (RA). Moreover,…
  • Abstract Number: 464 • 2015 ACR/ARHP Annual Meeting

    Biologic Therapy Treatment Complications in the Alberta Aboriginal Population with Rheumatoid Arthritis

    Cheryl Barnabe1, Yufei Zheng2, Arto Ohinmaa2, Brenda Hemmelgarn3, Gilaad Kaplan4, Liam Martin5 and Walter Maksymowych6, 1Cumming School of Medicine, University of Calgary, Calgary, AB, Canada, 2Institute of Health Economics, Edmonton, AB, Canada, 3Division of Nephrology, University of Calgary, Calgary, AB, Canada, 4Division of Gastroenterology, University of Calgary, Calgary, AB, Canada, 5Medicine, University of Calgary, Calgary, AB, Canada, 6Medicine, Medicine, University of Alberta, Edmonton, AB, Canada

    Biologic Therapy Treatment Complications in the Alberta Aboriginal Population with Rheumatoid Arthritis Background/Purpose: Aboriginal people with rheumatoid arthritis (RA) have more severe disease and an…
  • Abstract Number: 2612 • 2015 ACR/ARHP Annual Meeting

    Impact of a Multibiomarker Disease Activity Score in Patients with Rheumatoid Arthritis Treated in a Real World Setting

    Sergio Schwartzman1, Keith Knapp2, Gary Craig3, Karen Ferguson4 and Howard Kenney5, 1Rheumatology, Hospital for Special Surgery, New York, NY, 2Arthritis Northwest, Spokane, WA, 3Discus Analytics, Inc., Spokane, WA, 4Arthritis Northwest PLLC., Spokane, WA, 5Rheumatology, Arthritis Northwest, Spokane, WA

    Background/Purpose:   A number of composite outcome measures have been validated to quantify disease activity in Rheumatoid Arthritis (RA).  Few studies have been published on the…
  • Abstract Number: 570 • 2015 ACR/ARHP Annual Meeting

    Dose Selection of Namilumab, an Anti-GM-CSF Monoclonal Antibody: An Integrated Pharmacokinetic and Pharmacodynamic Approach for Phase II Studies in Patients with Rheumatoid Arthritis

    Thomas Wagner1, Ulrich Thienel2, Eva-Maria Vieser3, Bernard Souberbielle4 and Gezim Lahu1, 1Takeda Pharmaceuticals, Zurich, Switzerland, 2Takeda Pharmaceuticals, Deerfield, IL, 3AMGEN Research (Munich) GmbH, Munich, Germany, 4Takeda Pharmaceuticals, London, United Kingdom

    Background/Purpose: Granulocyte macrophage-colony stimulating factor (GM-CSF) mediates a range of immunological and inflammatory processes, and plays a role in a variety of inflammatory diseases. Namilumab…
  • Abstract Number: 2729 • 2015 ACR/ARHP Annual Meeting

    Clinical and Radiographic Outcome of Iguratimod for Rheumatoid Arthritis

    Tsuneo Kondo, Akiko Shibata, Ryota Sakai, Jun Kikuchi, Kentaro Chino, Ayumi Okuyama, Hirofumi Takei and Koichi Amano, Department of Rheumatology and Clinical Immunology, Saitama Medical Center, Saitama Medical University, Saitama, Japan

    Background/Purpose: Iguratimod is a new small-molecular drug for rheumatoid arthritis (RA), which was approved on June, 2012 in Japan. The agent inhibits the production of…
  • Abstract Number: 590 • 2015 ACR/ARHP Annual Meeting

    Expression Levels of Selected Genes May Predict Response to TNF Alpha Blockers or Rituximab in the Individual Rheumatoid Arthritis Patient

    Daphna Paran1, Shlomo Pundak2, Yaniv Kotler2, Yoav Smith3, Uri Arad4, David Levartovsky5, Ilana Kaufman4, Victoria Furer4, Ofir Elalouf4, Adi Broyde1, Sara Pel4, Dan Caspi4 and Ori Elkayam4, 1Rheumatology, Tel Aviv Sourasky Medical Center and the Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel, 2Genefron Ltd. Jerusalem Israel, Jerusalem, Israel, 3Genomic Data analysis Hadassah Medical School Hebrew University, Jerusalem Israel, Jerusalem, Israel, 4Rheumatology, Tel-Aviv Sourasky Medical Center and the Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel, 5Rheumatology, Tel-Aviv Sourasky Medical Center, Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel

    Background/Purpose: Patients with Rheumatoid arthritis (RA) have a variety of therapeutic options however tools to predict individual patients' response are limited. The purpose of this…
  • Abstract Number: 2776 • 2015 ACR/ARHP Annual Meeting

    Profiling Compounds in Human Primary Cell-Based Disease Models Guide Indication Selection

    Jason Ptacek, Ellen L. Berg and Alison O'Mahony, BioSeek, a division of DiscoveRx Corp., South San Francisco, CA

    Background/Purpose: In vitro co-cultures of human primary cells, including immune cells, fibroblasts, smooth muscle, keratinocytes, epithelial or endothelial cells were developed to capture the complexity…
  • Abstract Number: 611 • 2015 ACR/ARHP Annual Meeting

    The Rapid Kinetics of Optimal Treatment with Subcutaneous Methotrexate in Early Inflammatory Arthritis

    Anna O'Connor1, J Carter Thorne2, Diane Tin3 and Janet E. Pope4, 1Schulich School of Medicine and Dentistry, University of Western Ontario, London, ON, Canada, 2University of Toronto, Toronto, ON, Canada, 3The Arthritis Program, Southlake Regional Health Centre, Newmarket, ON, Canada, 4Monsignor Roney Bldg/Rheum, University of Western Ontario, St Joseph Health Care, London, ON, Canada

    Background/Purpose: Methotrexate (MTX) is standard treatment in RA. Absorption is better in subcutaneous MTX (scMTX), which may impact speed of onset. In RA, earlier time…
  • Abstract Number: 2783 • 2015 ACR/ARHP Annual Meeting

    What Is the Rate of Primary and Secondary Failure of Anti-TNF in RA Patients? Data from a Rheumatoid Arthritis Cohort

    Edward C. Keystone1, Mohammad Movahedi2,3, Angela Cesta2, Xiuying Li2, Sandra Couto2, Emmanouil Rampakakis3, John S. Sampalis3,4, Claire Bombardier2,5,6 and OBRI Investigators, 1The Rebecca MacDonald Centre For Arthritis, Mount Sinai Hospital, Toronto, ON, Canada, 2Toronto General Hospital Research Institute, University Health Network, Toronto, ON, Canada, 3JSS Medical Research, St-Laurent, QC, Canada, 4McGill University, Montreal, QC, Canada, 5University of Toronto, Department of Medicine (DOM) and Institute of Health Policy Management, and Evaluation (IHPME), Toronto, ON, Canada, 6Division of Rheumatology, Mount Sinai Hospital, Toronto, ON, Canada

    Background/Purpose: Although the majority of RA patients respond to treatment with anti-TNF agents, some patients present with refractory disease (1ry failure) while others show some…
  • Abstract Number: 969 • 2015 ACR/ARHP Annual Meeting

    Namilumab, an Anti-Granulocyte Macrophage-Colony Stimulating Factor (GM-CSF) Monoclonal Antibody: Results of the First Study in Patients with Mild-to-Moderate Rheumatoid Arthritis (RA)

    T. W. J. Huizinga1, Anastas Batalov2, Rumen Stoilov3, Eric Lloyd4, Thomas Wagner5, Didier Saurigny6, Bernard Souberbielle6 and Ehsanollah Esfandiari6, 1Rheumatology, Department of Rheumatology, Leiden University Medical Center, Leiden, Netherlands, 2UMHAT Kaspela, Plovdiv, Bulgaria, 3University Hospital (MHAT) St Ivan Rilski, Sofia, Bulgaria, 4Takeda Pharmaceuticals, Deerfield, IL, 5Takeda Pharmaceuticals, Zurich, Switzerland, 6Takeda Pharmaceuticals, London, United Kingdom

    Background/Purpose: GM-CSF mediates a range of immunological processes, such as stimulating the production of inflammatory mediators and differentiation of proinflammatory T-helper 17 cells, and may…
  • Abstract Number: 3194 • 2015 ACR/ARHP Annual Meeting

    Oral to Subcutaneous Methotrexate Dose-Conversion Strategies in the Treatment of Rheumatoid Arthritis

    Michael Schiff1 and Peter Sadowski2, 1Division of Rheumatology, University of Colorado, Denver, CO, 2Antares Pharma Inc., Minneapolis, MN

    Background/Purpose: Methotrexate (MTX) is the cornerstone of rheumatoid arthritis (RA) therapy1 but absorption saturation limitations compromise oral MTX bioavailability (BA). Subcutaneous (SC) MTX has a…
  • Abstract Number: 970 • 2015 ACR/ARHP Annual Meeting

    Efficacy and Safety of Sarilumab in Combination with Csdmards in Patients with Active Rheumatoid Arthritis Who Were Inadequate Responders or Intolerant of Anti–TNF-α Therapy: Results from a Phase 3 Study

    Roy Fleischmann1, Geraldo Castelar-Pinheiro2, Jan Brzezicki3, Pawel Hrycaj4, Yong Lin5, Janet van Adelsberg6, Neil Graham7, Hubert van Hoogstraten5, Deborah Bauer5 and Gerd Burmester8, 1University of Texas Southwestern Medical Center, Dallas, TX, 2Discipline of Rheumatology, Rio de Janeiro State University, Rio de Janeiro, Brazil, 3Centrum Kliniczno-Badawcze, Elblag, Poland, 4Poznan University of Medical Sciences, Poznan, Poland, 5Sanofi, Bridgewater, NJ, 6Clinical Science, Regeneron Pharmaceutials, Inc., Tarrytown, NY, 7Regeneron Pharmaceuticals, Inc., Tarrytown, NY, 8Department of Rheumatology and Clinical Immunology, Charité - Universitätsmedizin Berlin, Berlin, Germany

    Background/Purpose: The investigational agent sarilumab is a human mAb directed against the IL-6 receptor. The phase 3 MOBILITY study (NCT01061736) evaluated the efficacy and safety…
  • Abstract Number: 3243 • 2015 ACR/ARHP Annual Meeting

    A Randomized Controlled Trial for a Physical Activity Intervention for RA Fatigue

    Patricia P. Katz1, Mary Margaretten2, Steven Gregorich1, Sandi Kaplan3, Stephanie Rush4 and Laura Trupin1, 1Medicine, University of California San Francisco, San Francisco, CA, 2Medicine, University of California, San Francisco, San Francisco, CA, 3Arthritis Research Group, University of California, San Francisco, CA, 4University of California, San Francisco, San Francisco, CA

    Background/Purpose: Fatigue is a major problem for people with RA.  Physical inactivity is an indirect risk factor for fatigue1. We tested the effect of a…
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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.).

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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