ACR Meeting Abstracts

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Abstracts tagged "Adalimumab"

  • Abstract Number: 2853 • 2014 ACR/ARHP Annual Meeting

    Comparative Study of Infliximab Versus Adalimumab in Patients with Refractory Uveitis Due to Behçet´s Disease. Multicenter Study of 125 Cases

    Leyre Riancho-Zarrabeitia1, Vanesa Calvo-Río1, Ricardo Blanco1, Paz Rodríguez-Cundín2, Emma Beltrán3, Juan Sánchez Bursón Sr.4, Marina Mesquida5, Alfredo Adan5, M. Victoria Hernández6, Marisa Hernandez Grafella7, Elia Valls Pascual8, Lucía Martinez-Costa9, Agusti Sellas-Fernandez10, Miguel Cordero-Coma11, Manuel Díaz-Llopis12, Roberto Gallego12, Jose Luis García Serrano13, Norberto Ortego-Centeno14, Jose M Herreras15, Alejandro Fonollosa16, Angel M. Garcia-Aparicio17, Olga Maiz Alonso18, Ana Blanco19, Ignacio Torre Salaberri20, Cruz Fernández- Espartero21, Vega Jovani22, Diana Peiteado23, Esperanza Pato24, Juan Cruz25, Carlos Férnandez Cid26, Elena Aurrecoechea27, Miriam García-Arias28, Miguel Angel Caracuel-Ruiz29, Carlos Alberto Montilla Morales30, Antonio Atanes-Sandoval31, Félix Francisco32, Santos Insua33, Senen González-Suárez34, Maria Amalia Sanchez Andrade35, Fernando Gamero36, Luis Francisco Linares Ferrando37, Fredeswinda Romero38, A. Javier García-González39, Raquel Almodóvar González40, Enrique Minguez41, Carmen Carrasco Cubero42, Alejandro Olive43, Julio Vázquez44, Oscar Ruiz Moreno45, Fernando Jiménez-Zorzo45, Javier Manero45, Santiago MuÑoz Fernandez46, Javier Rueda-Gotor1, Trinitario Pina1, Montserrat Santos-Gómez1 and Miguel A. González-Gay1, 1Rheumatology, Hospital Universitario Marqués de Valdecilla. IDIVAL. Santander. Spain, Santander, Spain, 2Preventive Medicine, Hospital Universitario Marqués de Valdecilla. IDIVAL. Santander. Spain, Santander, Spain, 3Rheumatology, Hospital General Universitario de Valencia. Spain, Valencia, Spain, 4Rheumatology. Hospital de Valme., Sevilla, Spain, 5Ophthalmology, Hospital Clinic. Barcelona. Spain, Barcelona, Spain, 6Arthritis Unit, Department of Rheumatology, Hospital Clinic, Barcelona, Barcelona, Spain, 7Ophthalmology. Hospital General universitario de Valencia, Valencia, Spain, 8Rheumatology. Hospital Peset, Valencia, Spain, 9Ophthalmology. Hospital Peset, Valencia, Spain, 10H. Vall d'Hebron, Barcelona, Spain, 11Ophthalmology, Hospital de León. Spain, León, Spain, 12Ophthalmology, Hospital Universitario La Fe. Valencia. Spain, Valencia, Spain, 13Ophthalmology. Hospital San Cecilio, Granada, Spain, 14Systemic Autoimmune Diseases Unit, Hospital Clínico San Cecilio, Granada, Spain, 15Ophthalmology. Hospital Universitario, IOBA, Valladolid, Spain, 16Ophthalmology, Hospital de Cruces. Bilbao. Spain, Bilbao, Spain, 17Rheumatology, Virgen de la Salud Hospital, Toledo, Spain, 18Rheumatology, Hospital Universitario de Donostia. San Sebastián. Spain, San Sebastián, Spain, 19Ophthalmology. Hospital Donosti, San Sebastián, Spain, 20Rheumatology, Hospital Universitario de Basurto. Bilbao. Spain, Bilbao, Spain, 21Rheumatology, Hospital Universitario de Móstoles. Madrid. Spain, Madrid, Spain, 22Rheumatology. Hospital General de Alicante, Alicante, Spain, 23Rheumatology, Hospital La Paz - IdiPaz, Madrid, Spain, 24Rheumatology. Hospital Clínico San Carlos, Madrid, Spain, 25Rheumatology. Hospital de Pontevedra, Pontevedra, Spain, 26Ophthalmology. Hospital de Pontevedra, Pontevedra, Spain, 27Hospital Sierrallana. Torrelavega, Torrelavega, Spain, 28Rheumatology, Hospital Universitario de La Princesa. IIS La Princesa, Madrid, Spain, 29Plaza Cruz Roja, 1, H. Reina Sofia, Cordoba, Spain, 30Hospital Clínico Universitario de Salamanca, Salamanca, Spain, 31Rheumatology Division. C. Hospitalario Universitario A Coruña, A Coruña, Spain, 32Rheumatology, Hospital Doctor Negrín. Las Palmas de Gran Canaria. Spain, Las Palmas de Gran Canaria, Spain, 33Rheumatology. Hospital Universitario Santiago de Compostela, A Coruña, Spain, 34Rheumatology. Hospital Cabueñes, Gijón, Spain, 35Hosp. Lucus Augusti, Lugo, Spain, 36Rheumatology. Hospital San Pedro Alcantara, Cáceres, Spain, 37Rheumatology, Hospital Virgen de la Arrixaca. Murcia. Spain, Murcia, Spain, 38Rheumatology, Jiménez Díaz Foundation University Hospital, Madrid, Spain, 39Servicio de Reumatología, Instituto de Investigación Hospital 12 de Octubre (I+12), Madrid, Spain, 40Rheumatology Unit, Hospital Universitario Fundación Alcorcón, Madrid, Spain, 41Ophthalmology. Hospital Clínico de Zaragoza, Zaragoza, Spain, 42Rheumatology, Hospital de Merida, Mérida, Spain, 43Rheumatology Service, Germans Trias Pujol Hospital, Barcelona, Spain, 44Rheumatology. Hospital de Ferrol, A Coruña, Spain, 45Ophthalmology and Rheumatology. Hospital Miguel Servet Zaragoza, Spain, Zaragoza, Spain, 46Sección de Reumatología, Hospital Universitario Infanta Sofía, San Sebastián de los Reyes, Madrid, Spain

    Background/Purpose: To compare the efficacy of infliximab (IFX) versus adalimumab (ADA) as first biologic drug in refractory uveitis due to Behçet's disease (BD) for 1-year…
  • Abstract Number: 561 • 2014 ACR/ARHP Annual Meeting

    A Psychometric Analysis of Outcome Measures in Trials of Peripheral Spondyloarthritis

    Sofia Ramiro1, Maureen C. Turina2, Dominique L. Baeten3, Philip J. Mease4, Jacqueline E. Paramarta2, In-Ho Song5, Aileen L. Pangan6 and Robert Landewé7, 1Clinical Immunology and Rheumatology, Amsterdam Rheumatology Center/University of Amsterdam, Amsterdam, Netherlands, 2Department of Clinical Immunology and Rheumatology, Academic Medical Center/University of Amsterdam, Amsterdam, Netherlands, 3Department of Clinical Immunology and Rheumatology and Department of Experimental Immunology, Academic Medical Centre/University of Amsterdam, Amsterdam, Netherlands, 4Division of Rheumatology Research, Swedish Medical Center and University of Washington, Seattle, WA, 5AbbVie Deutschland GmbH & Co. KG, Ludwigshafen, Germany, 6AbbVie Inc., North Chicago, IL, 7Division of Clinical Immunology and Rheumatology, Academic Medical Center/University of Amsterdam, Amsterdam, Netherlands

    Background/Purpose: We assessed the discriminatory aspects of disease activity measures and response criteria between adalimumab (ADA) and placebo (PBO) in 2 studies of patients (pts)…
  • Abstract Number: 2581 • 2014 ACR/ARHP Annual Meeting

    Clinically Active Non-Radiographic Axial Spondyloarthritis Patients Who Initially Have a Negative MRI and Normal CRP May Develop a Positive MRI or Elevated CRP at a Later Timepoint

    Xenofon Baraliakos1, Joachim Sieper2, Su Chen3, Aileen L. Pangan3 and Jaclyn K. Anderson3, 1Rheumazentrum Ruhrgebiet, Herne, Germany, 2Charité Universitätsmedizin Berlin, Berlin, Germany, 3AbbVie Inc., North Chicago, IL

    Background/Purpose: Patients (pts) with non-radiographic axial spondyloarthritis (nr-axSpA) and active disease may have objective evidence of inflammation, either as bone marrow edema (BME) on magnetic…
  • Abstract Number: 567 • 2014 ACR/ARHP Annual Meeting

    Use of Monotherapy Anti-Tnf Agents in Ankylosing Spondylitis Patients from the rhumadata® Registry: 8-Year Comparative Effectiveness of Adalimumab, Etanercept and Infliximab

    Denis Choquette1, Louis Bessette2, Isabelle Fortin3, Boulos Haraoui1, Jean Pierre Pelletier1, Jean-Pierre Raynauld1, Diane Sauvageau1, Edith Villeneuve1 and Louis Coupal1, 1Rheumatology, Institut de rhumatologie de Montréal (IRM), Montréal, QC, Canada, 2Rheumatology, Centre d’ostéoporose et de rhumatologie de Québec (CORQ), Québec, QC, Canada, 3Centre de rhumatologie de l'est du Québec (CREQ), Rimouski, QC, Canada

    Background/Purpose: Anti-TNF agents namely adalimumab (ADA), etanercept (ETA) and infliximab (INF) are approved for the treatment of signs and symptoms of ankylosing spondylitis. Their efficacy…
  • Abstract Number: 2517 • 2014 ACR/ARHP Annual Meeting

    Long-Term Clinical, Structural, and Functional Consequences of Not Adopting Treatment in MTX Suboptimal Responders

    Josef Smolen1, Ronald F. van Vollenhoven2, Stefan Florentinus3, Yijie Zhou4, Benoit Guerette4 and Arthur Kavanaugh5, 1Medical University of Vienna and Hietzing Hospital, Vienna, Austria, 2The Karolinska Institute, Stockholm, Sweden, 3AbbVie, Rungis, France, 4AbbVie, Inc., North Chicago, IL, 5University of California San Diego, La Jolla, CA

    Background/Purpose: Methotrexate (MTX) is used as first line therapy for treatment of rheumatoid arthritis (RA). Current recommendations state that therapy should be adjusted if patients…
  • Abstract Number: 558 • 2014 ACR/ARHP Annual Meeting

    Therapeutic Response in Adalimumab-Treated Patients with Non-Radiographic Axial Spondyloarthritis Is Similar Regardless of Body Mass Index

    Philip J. Mease1, Denis Poddubnyy2, Su Chen3 and Jaclyn K. Anderson3, 1Swedish Medical Center and University of Washington, Seattle, WA, 2Charité Universitätsmedizin Berlin, Berlin, Germany, 3AbbVie Inc., North Chicago, IL

    Background/Purpose: C-reactive protein (CRP), an objective measure of active inflammation, has been associated with obesity, with both overweight and obese individuals more likely to have…
  • Abstract Number: 2510 • 2014 ACR/ARHP Annual Meeting

    Good Response to Methotrexate (MTX) and/or MTX Plus Adallimumab (ADA): 3 Yrs Study Results in Patients with Rheumatoid Arthritis (RA)

    Kazuko Shiozawa1, Takashi Yamane2, Miki Murata1, Chihiro Tanaka1, Noriaki Yo2, Ryosuke Yoshihara1, Yasushi Tanaka1, Ken Tsumiyama3 and Shunichi Shiozawa4, 1The Rheumatic Diseases Center, Kohnan Kakogawa Hospital, Kakogawa, Japan, 2Kohnan Kakogawa Hospital, Kakogawa, Japan, 3Department of Rheumatology, Kyushu University Beppu Hospital, Beppu, Japan, 4Department of Medicine, Rheumatic Diseases Unit, Kyushu University Beppu Hospital, Beppu, Japan

    Background/Purpose: To achieve comprehensive disease control (CDC; defined as simultaneous achievement of DAS28 < 3.2, HAQ-DI < 0.5 and ΔmTSS ≤ 0.5) or comprehensive disease…
  • Abstract Number: 553 • 2014 ACR/ARHP Annual Meeting

    Comparison of Baseline Extra-Articular Manifestations, Comorbidities, and Long-Term Safety in Patients Treated with Adalimumab for Ankylosing Spondylitis and Non-Radiographic Axial Spondyloarthritis

    Joachim Sieper1, Désirée van der Heijde2, Nupun A. Varothai3 and Jaclyn K. Anderson3, 1Charité Universitätsmedizin Berlin, Berlin, Germany, 2Department of Rheumatology, Leiden University Medical Center, Leiden, Netherlands, 3AbbVie Inc., North Chicago, IL

    Background/Purpose: To compare 1) extra-articular manifestations, 2) baseline comorbidities, and 3) adverse event (AE) rates with long-term adalimumab (ADA) therapy in patients (pts) treated in…
  • Abstract Number: 2509 • 2014 ACR/ARHP Annual Meeting

    ADAM-10 As a Tocilizumab Treatment Predictive Factor in Rheumatoid Arthritis

    Takeo Isozaki, Sakiko Isojima, Takahiro Tokunaga, Masayu Umemura, Hidekazu Furuya, Ryo Yanai, Ryo Takahashi, Kuninobu Wakabayashi, Nobuyuki Yajima, Yusuke Miwa and Tsuyoshi Kasama, Div of Rheumatology, Showa University School of Med, Shinagawa-ku Tokyo, Japan

    Background/Purpose :A disintegrin and metalloproteinases (ADAMs) are a family of transmembrane and secreted proteins. ADAM-10 has been reported to be the enzyme responsible for the…
  • Abstract Number: 502 • 2014 ACR/ARHP Annual Meeting

    Tocilizumab Use in Patients with Rheumatoid Arthritis Having Failed One Previous Anti-TNF Agent: Comparison with Adalimumab, Etanercept and Infliximab

    Denis Choquette1, Marie-Pier Payette1, Jean-Pierre Raynauld1, Jean-Pierre Pelletier2, Louis Bessette3, Edith Villeneuve1, Boulos Haraoui1, Isabelle Fortin4, Marie-Anaïs Rémillard5, Diane Sauvageau1 and Louis Coupal1, 1Rheumatology, Institut de rhumatologie de Montréal (IRM), Montréal, QC, Canada, 2Osteoarthritis Research Unit, University of Montreal Hospital Research Centre (CRCHUM), Montreal, QC, Canada, 3Rheumatology, Centre d’ostéoporose et de rhumatologie de Québec (CORQ), Québec, QC, Canada, 4Centre de rhumatologie de l'est du Québec (CREQ), Rimouski, QC, Canada, 5Rhumatology, Institut de rhumatologie de Montréal (IRM), Montréal, QC, Canada

    Background/Purpose : Tocilizumab, as an intra-venous agent, has been approved for rheumatoid arthritis (RA) in Canada in April 30th, 2010. It was the sixth approved…
  • Abstract Number: 2427 • 2014 ACR/ARHP Annual Meeting

    Attainment of Low Disease Activity Is Predictive of Maintenance of Disease Control upon Adalimumab Discontinuation for Two Years Following Combination Therapy in Japanese Patients with Early Rheumatoid Arthritis

    Yoshiya Tanaka1, Hisashi Yamanaka2, Naoki Ishiguro3, Nobuyuki Miyasaka4, Katsuyoshi Kawana5, Katsutoshi Hiramatsu6, Aki Kuroki5 and Tsutomu Takeuchi7, 1University of Occupational and Environmental Health, Japan, Kitakyushu, Japan, 2Institute of Rheumatology, Tokyo Women’s Medical University, Tokyo, Japan, 3Orthopaedic Surgery and Rheumatology, Nagoya University Graduate School of Medicine, Nagoya, Japan, 4Tokyo Medical and Dental University, Tokyo, Japan, 5Abbvie, Tokyo, Japan, 6Medical, Abbvie, Tokyo, Japan, 7Division of Rheumatology, Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan

    Background/Purpose: Although available data has suggested successful withdrawal of a monoclonal antibody TNF blocker after achieving low disease activity (LDA) or remission over the short-term…
  • Abstract Number: 500 • 2014 ACR/ARHP Annual Meeting

    Prediction of Successful Dose Reduction or Discontinuation of Adalimumab or Etanercept Using Serum Drug Levels and Antidrug Antibody Measurement

    Noortje van Herwaarden1, Chantal Bouman2, Aatke van der Maas3, Ronald F. van Vollenhoven4, Johannes W.J. Bijlsma5, Frank H.J. van den Hoogen6, Alfons A. den Broeder1 and Bart van den Bemt7, 1Rheumatology, Sint Maartenskliniek, Nijmegen, Netherlands, 2Sint Maartenskliniek, Nijmegen, Netherlands, 3Hengstdal 3, Sint Maartenskliniek, Nijmegen, Netherlands, 4Unit for clinical therapy research (ClinTrid), Karolinska Institute, Stockholm, Sweden, 5Department of Rheumatology and Clinical Immunology, University Medical Center Utrecht, Utrecht, Netherlands, 6Rheumatology, Rheumatology Centre Sint Maartenskliniek and Radboud university medical center, Ubbergen (Nijmegen), Netherlands, 7Pharmacy, Sint Maartenskliniek, Nijmegen, Netherlands

    Background/Purpose Dose reduction and discontinuation of TNF inhibitors (TNFi) is feasible in many rheumatoid arthritis (RA) patients, but leads to (temporary) worsening of disease activity…
  • Abstract Number: 2393 • 2014 ACR/ARHP Annual Meeting

    Similar Improvements in Physical Function, Quality of Life and Work Productivity Among Rheumatoid Arthritis Patients Treated with 2 Different Doses of Methotrexate  in Combination with Adalimumab

    Gurjit S. Kaeley1, Midori Jane Nishio2, Daryl MacCarter3, Jenny Griffith4, Hartmut Kupper5, Vishvas Garg6 and Jasmina Kalabic5, 1College of Medicine, University of Florida, Jacksonville, FL, 2Diablo Clinical Research, Walnut Creek, CA, 3Coeur d'Alene Arthritis Clinic, Coeur d'Alene, ID, 4AbbVie, Inc., North Chicago, IL, 5AbbVie Deutschland GmbH & Co. KG, Ludwigshafen, Germany, 6AbbVie Inc., North Chicago, IL

    Background/Purpose Methotrexate (MTX) is used in monotherapy or in combination with other DMARDs in the treatment of patients (pts) with rheumatoid arthritis (RA). We evaluated…
  • Abstract Number: 490 • 2014 ACR/ARHP Annual Meeting

    A Randomised Controlled Trial Evaluating the Effect of Humira upon Endothelial Function in ACPA Positive Rheumatoid Arthritis – an Interim Analysis

    Stephen Oakley1,2,3, Niloofar Esmaili4, Gabor Major4, David Mathers4,5, Siva Ratnarajah6, John van der Kallen5, Mark Collins6, Marc Toh6 and John Glass4, 1Dept of Rheumatology, Newcastle Bone & Joint Institute, Newcastle, Australia, 2School of Medicine & Public Health, University of Newcastle, Newcastle, Australia, 3Clinical Trials Unit, Hunter Medical Research Institute, Newcastle, Australia, 4Rheumatology, Newcastle Bone & Joint Institute, Newcastle, Australia, 5Rheumatology, Georgetown Arthritis Centre, Newcastle, Australia, 6Rheumatology, Private Practice, Newcastle, Australia

    Background/Purpose Rheumatoid arthritis (RA) is associated with elevated cardiovascular (CV) risk not explained by traditional risk factors. Increased CV risk may develop prior to the…
  • Abstract Number: 2043 • 2014 ACR/ARHP Annual Meeting

    How Correct Are the Assumptions Made for Tuberculosis Screening Algorythms before TNF-Alpha Antagonists?

    Aysa Hacioglu1, Yesim Ozguler2, Sermin Borekci3, Vedat Hamuryudan1, Hanefi Deniz Kecebas1, Ethem Koray Tascilar2, Melike Melikoglu4, Serdal Ugurlu1, Emire Seyahi1, Izzet Fresko2, Huri Ozdogan1, Sebahattin Yurdakul1, Gul Ongen3 and Gulen Hatemi1, 1Division of Rheumatology, Department of Internal Medicine, Cerrahpasa Medical Faculty, University of Istanbul, Istanbul, Turkey, 2University of Istanbul, Cerrahpasa Medical Faculty, Rheumatology, Istanbul, Turkey, 3University of Istanbul, Cerrahpasa Medical Faculty, Department of Pulmonary Diseases, Istanbul, Turkey, 4Istanbul University, Cerrahpasa Medical Faculty, Rheumatology, Istanbul, Turkey

    Background/Purpose: During the development of algorythms for screening latent tuberculosis before starting TNF-alpha antagonists, it is assumed that BCG vaccination causes false positive PPD and…
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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.

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Accepted abstracts are made available to the public online in advance of the meeting and are published in a special online supplement of Arthritis & Rheumatology. Information contained in those abstracts may not be released until the abstracts appear online. 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 a scientific presentation or presentation of additional new information that will be available at the time of the meeting) is under embargo until Saturday, November 11, 2023.

Violation of this policy may result in the abstract being withdrawn from the meeting and other measures deemed appropriate. Authors are responsible for notifying financial and other sponsors about this policy. If you have questions about the abstract embargo policy, please contact the public relations department at [email protected].

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