ACR Meeting Abstracts

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Abstracts tagged "Biologicals"

  • Abstract Number: 2474 • ACR Convergence 2023

    Uveitis as Predictor of Disease Flare After the First Course of Anti-TNF Withdrawal in Oligo and Polyarticular Juvenile Idiopathic Arthritis: A Multicentric Italian Experience

    Ilaria Maccora1, Valerio Accardo2, Marco Cattalini3, ilaria Pagnini4, Andrea Taddio5, Edoardo Marrani6, francesco La Torre7, Matteo Trevisan8, Maria Vincenza Mastrolia9 and Gabriele Simonini10, 1PhD student, in the Area of Drugs and Innovative Treatments, NeuroFARBA Department, University of Florence. Meyer Children's Hospital, Firenze, Italy, 2University of Florence, Florence, Italy, 3Spedali Civili di Brescia, Brescia, Italy, 4Meyer Children's Hospital IRCCS, Florence, Italy, 5Rheumatology Unit, IRCCS Burlo Garofalo, Trieste, Italy, 6University of Florence, Firenze, Italy, 7Giovanni XXIII Pediatric Hospital, University of Bari, Bari, Italy, 8IRCCS Burlo Garofalo, Trieste, Italy, 9NEUROFARBA Department, University of Florence, Florence, Italy, 10Rheumatology Unit, ERN ReConnet Center, Meyer Children's Hospital IRCCS, Florence Italy. NeuroFARBA Department, University of Florence, Florence, Italy

    Background/Purpose: TNF inhibitors (TNFi) have dramatically changed the prognosis of Juvenile Idiopathic Arthritis (JIA). However, once achieved disease remission, it is not clear how and…
  • Abstract Number: 0346 • ACR Convergence 2023

    Use, Safety and Persistence of Biosimilars in Adult Patients Diagnosed with Juvenile Idiopathic Arthritis: Results from the Spanish Registry of Adverse Events of Targeted Therapies in Rheumatic Diseases (BIOBADASER)

    Juan José Bethencourt1, Lucia Otero-Valera2, JAVIER MANERO3, Eva Perez-Pampin4, Yanira Pérez Vera5, SARA MANRIQUE6, Maria Sagrario Bustabad Reyes7, Mercedes Freire González8, Dolores Ruiz-Montesinos9, Lourdes Mateo Soria10, Raquel Martín Domenech11, Manuel Moreno Ramos12, Fernando Alonso2 and Isabel Castrejon13, 1Hospital Universitario de Canarias, Santa Cruz de Tenerife, Spain, 2Spanish Society of Rheumatology, Madrid, Spain, 3Department of Rheumatology, Hospital Universitario Miguel Servet, Zaragoza, Spain, 4Rheumatology Department Complejo Hospitalario Universitario Santiago, Santiago de compostela, Spain, 5Hospital Universitario Dr Negrín, Las Palmas de Gran Canaria, Spain, 6Division of Rheumatology, Hospital Regional Universitario Carlos Haya, Malaga, Spain, 7Hospital Universitario de Canarias, La Laguna, Spain, 8Rheumatology department, Complexo Hospitalario Universitario A Coruña (CHUAC). Instituto de Investigación Biomédica A Coruña (INIBIC), A Coruña, Spain, 9Hospital Universitario Virgen Macarena, Sevilla, Spain, 10HOSPITAL GERMANS TRIAS I PUJOL, Badalona, Spain, 11Hopsital General de Elda, Alicante, Spain, 12Hospital Clínico Universitario Virgen dela Arrixaca, Murcia, Spain, 13Hospital General Universitario Gregorio Marañón, Madrid, Spain

    Background/Purpose: Juvenile idiopathic arthritis (JIA) is the most common chronic rheumatic disease of childhood. The emergence of new biologic agents has led to changes in…
  • Abstract Number: 0445 • ACR Convergence 2023

    Comparison of the Efficacy, Safety and Immunogenicity of a Proposed Biosimilar MSB11456 with Tocilizumab Reference Product in Moderate-to-severe Rheumatoid Arthritis: Results of a Randomized Double-blind Study

    Anna Zubrzycka-Sienkiewicz1, Maria Misterska-Skora2, Małgorzata Socik Pojawa3, Kamilla Klama4, Martin Ullmann5, Corinne Petit-Frere5, Andras Illes5, Peter Baker5, Joëlle Monnet5 and Jan Brzezicki6, 1Reumatika - Centrum Reumatologil, Warsaw, Poland, 2Centrum Medyczne Oporów, Wrocław, Poland, 3MICS Centrum Medyczne Warszawa, Warsaw, Poland, 4Solumed Centrum Medyczne, Poznań, Poland, 5Fresenius Kabi SwissBiosimilars, Eysins, Switzerland, 6Centrum Kliniczno Badawcze, Elbląg, Poland

    Background/Purpose: Tocilizumab is an anti‑interleukin‑6 receptor monoclonal antibody indicated for treating rheumatoid arthritis (RA) and other inflammatory diseases. MSB11456 is a proposed biosimilar to US‑licensed…
  • Abstract Number: 0582 • ACR Convergence 2023

    Evaluation of Anifrolumab Treatment Responses by the Short Form 36 Health Survey Version 2 in SLE: A Post Hoc Analysis of the Placebo-Controlled Phase 3 Long-Term Extension Trial

    Vibeke Strand1, Kenneth Kalunian2, Barnabas Desta3, Caroline Seo4, Gabriel Abreu5, Raj Tummala3, Catharina Lindholm5 and Hussein Al-Mossawi6, 1Stanford University, Palo Alto, CA, 2University of California San Diego, La Jolla, CA, 3BioPharmaceuticals R&D, AstraZeneca, Gaithersburg, MD, 4BioPharmaceuticals Medical Evidence, AstraZeneca, Gaithersburg, MD, 5BioPharmaceuticals R&D, AstraZeneca, Gothenburg, Sweden, 6BioPharmaceuticals R&D, AstraZeneca, Cambridge, United Kingdom

    Background/Purpose: SLE is a chronic disease that progressively reduces patients’ health-related quality of life.1 In a post hoc analysis of the TULIP trials, patients with…
  • Abstract Number: 0784 • ACR Convergence 2023

    Kidney-Related Outcomes and Steroid-Sparing Effects in Patients with Active Lupus Nephritis Treated with Obinutuzumab: A Post Hoc Analysis of a Phase 2 Trial

    Brad Rovin1, Jorge Ross Terres2, Sophia Giang3, Thomas Schindler4, Armando Turchetta5, Jay Garg2, Richard Furie6, William F. Pendergraft III2 and Ana Malvar7, 1Ohio State University, Columbus, OH, 2Genentech, Inc., South San Francisco, CA, 3Genentech, Inc., San Francisco, CA, 4F. Hoffmann-La Roche Ltd, Basle, Switzerland, 5F. Hoffmann-La Roche Ltd, Basel, Switzerland, 6Northwell Health, Manhasset, NY, 7Hospital Fernandez, Buenos Aires, Argentina

    Background/Purpose: Preservation of long-term kidney function and sustained reduction of glucocorticoid use are major therapeutic goals in lupus nephritis (LN). In the randomized, double-blind, placebo-controlled,…
  • Abstract Number: 1107 • ACR Convergence 2023

    Predictors of Pegloticase Urate-lowering Response in the Presence and Absence of Methotrexate Co-therapy

    James Mossell1, Mai Duong2, Katie Obermeyer2, Lissa Padnick-Silver2, Brian LaMoreaux2 and Sanjay Chabra3, 1Arthritis and Osteoporosis Center of South Georgia, Tifton, GA, 2Horizon Therapeutics, Deerfield, IL, 3Texas Arthritis Center, El Paso, TX

    Background/Purpose: Pegloticase can lower serum urate (SU) in patients with uncontrolled gout who are refractory to/intolerant of oral urate-lowering therapies. However, antidrug antibodies (ADAs) can…
  • Abstract Number: 1330 • ACR Convergence 2023

    Certolizumab-pegol, Abatacept, Tocilizumab or Active Conventional Therapy in Early Rheumatoid Arthritis: 48 Week Patient-reported Outcomes of the NORD-STAR Trial

    John Lampa1, Dan Nordstrom2, Ronald van Vollenhoven3, Merete Hetland4, Espen A Haavardsholm5, Mikkel Østergaard6, Anna Rudin7, Marte Schrumpf Heiberg5, Michael Nurmohamed3, Bjorn Gudbjornsson8, Kristina Lend9, Kim Hørslev-Petersen10, Tuulikki Sokka-Isler11, Gerdur Maria Grondal12, Simon Krabbe13, Joakim Lindqvist14, Anna-Karin Hultgård Ekwall15, Daniel Glinatsi16, Meliha Kapetanovic17, Cidem Gentline14, Anna-Birgitte Aga18, Heikki Relas2, Tove Lorenzen19, Giovanni Cagnotto20, Johan Back21, Oliver Hendricks22, Bas Dijkshoorn23, Kajsa Öberg24, Maud-Kristine Aga Ljoså25, Eli Brodin26, Hanne Merete Lindegaard27, Annika Söderbergh28, Milad Rizk29, Alf Kastbom30, Per Larsson31, Line Uhrenholt32, Søren Just33, David J Stevens34, Trine B Laurberg35, Gunnstein Bakland36, Inge Olsen37, Joseph Sexton18 and Till Uhlig18, 1Stockholm County, Hãsselby, Sweden, 2Helsinki University Hospital, Helsinki, Finland, 3Amsterdam University Medical Centers, Amsterdam, Netherlands, 4Copenhagen Center for Arthritis Research, Rigshospitalet, Copenhagen, Denmark, 5Diakonhjemmet Hospital, Oslo, Norway, 6Copenhagen Center for Arthritis Research, Center for Rheumatology and Spine Diseases, Centre for Head and Orthopaedics, Rigshospitalet; University of Copenhagen, Copenhagen, Denmark, 7Department of Rheumatology and Inflammation Research, Institute of Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden, 8Centre for Rheumatology Research, University Hospital, Reykjavik, Iceland, 9Amsterdam UMC, Karolinska Institute, Stockholm, Sweden, 10University of Southern Denmark, Odense, Denmark, 11Jyvaskyla Central Hospital, Jyväskylä, Finland, 12Department for Rheumatology, Landspitali University Hospital, Reykjavik, Iceland, 13Herlev-Gentofte University Hospital, Herlev, Denmark, 14Karolinska University Hospital, Stockholm, Sweden, 15Department of Rheumatology and Inflammation research, Sahlgrenska Academy, University of Gothenburg, Kullavik, Sweden, 16Copenhagen Center for Arthritis Research, Rigshospitalet, Copenhagen, Sweden, 17Lund University and Skåne University Hospital, Lund, Sweden, 18Center for Treatment of Rheumatic and Musculoskeletal Diseases (REMEDY), Diakonhjemmet Hospital, Oslo, Norway, 19Silkeborg University Hospital, Silkeborg, Denmark, 20Skåne University Hospital, Lund, Sweden, 21Uppsala University Hospital, Uppsala, Sweden, 22Danish Hospital for Rheumatic Diseases, Sønderborg, Denmark, 23Amsterdam Rheumatology and Immunology Center, Location Reade, Amsterdam, Netherlands, 24Falu Hospital, Falun, Sweden, 25Ålesund Hospital, Ålesund, Norway, 26Haukeland University Hospital, Bergen, Norway, 27Odense Hospital, Odense, Denmark, 28Örebro University Hospital, Örebro, Sweden, 29Västmanlands Hospital Västerås, Västerås, Sweden, 30Linköping University, Linköping, Sweden, 31Academic Specialist Center, Stockholm, Sweden, 32Aalborg University Hospital, Aalborg, Denmark, 33Section of Rheumatology, Department of Medicine, Odense University Hospital – Svendborg Hospital, Odense, Denmark, 34St. Olavs Hospital, Trondheim, Norway, 35Aarhus University Hospital, Aarhus, Denmark, 36University Hospital of North Norway, Tromsø, Norway, 37Oslo University Hospital, Oslo, Norway

    Background/Purpose: The optimal first-line treatment of patients with early rheumatoid arthritis (eRA) is not established. Methods: In this investigator-initiated, randomized, open-label study (NCT01491815), patients with…
  • Abstract Number: 1499 • ACR Convergence 2023

    Year-5 Follow-up of Belimumab Safety (mortality and Malignancies) in Patients with Systemic Lupus Erythematosus (SLE) Who Completed a Phase 4, 52-week, Randomized, Double-blind Placebo-controlled Safety Study

    Saira Sheikh1, James Cheng-Chung Wei2, Dana Tegzova3, William Stohl4, Ricardo Acayaba de Toledo5, Tamara Mucenic6, Mauricio R. Abello Banfi7, Kathleen Maksimowicz-McKinnon8, Carlos Abud-Mendoza9, Sandra Navarra10, Mercedes García11, IGNACIO GARCÍA-DE LA TORRE12, Sofia Fernandes13, Julia HN Harris14, Abhishek Roy15, Jose Miyar Olaiz16, Paul WIlde17 and David A. Roth18, 1University of North Carolina at Chapel Hill, Chapel Hill, NC, 2Chung Shan Medical University Hospital, Department of Rheumatology, Taichung, Taiwan, 3Institute of Rheumatology, Prague, Czech Republic, 4University of Southern California Keck School of Medicine, Division of Rheumatology, Los Angeles, CA, 5Faculdade de Medicina de São José do Rio Preto, São José do Rio Preto, Service of Rheumatology of the Internal Medicine Department, São José do Rio Preto, Brazil, 6Hospital Moinhos de Vento, Porto Alegre, Brazil, 7Centro Integral de Reumatología del Caribe, Barranquilla, Colombia, 8Medical University of South Carolina, Charleston, SC, 9Hospital Central “Dr Ignacio Morones Prieto”, Unidad Regional de Reumatología y Osteoporosis, Hospital Central; Facultad de Medicina de la Universidad Autónoma de San Luis Potosí, San Luis Potosí, Mexico, 10University of Santo Tomas Hospital, Joint and Bone Center, Manila, Philippines, 11Hospital Interzonal General de Agudos José de San Martín, La Plata, Argentina, 12Universidad de Guadalajara/Hospital General de Occidente, Guadalajara, Mexico, 13GlaxoSmithKline, Stevenage, United Kingdom, 14GlaxoSmithKline, Immunology Biostatistics, Brentford, United Kingdom, 15GlaxoSmithKline, Bangalore, India, 16GlaxoSmithKline, Safety Evaluation and Risk Management, Brentford, United Kingdom, 17GlaxoSmithKline, Clinical Development, Brentford, United Kingdom, 18GlaxoSmithKline, Collegeville, PA

    Background/Purpose: Belimumab (BEL) is an approved treatment for active SLE and LN, in addition to standard therapy (ST). Despite BEL clinical studies demonstrating a favorable…
  • Abstract Number: 1815 • ACR Convergence 2023

    The Association of Body Mass Index with SARS-CoV-2 Infection (COVID-19) in Patients with Inflammatory Arthritis on Biologic Disease Modifying Anti-Rheumatic Drugs: Results from the Singapore National Biologics Register

    Preeti Dhanasekaran1, Margaret Ma2, Manjari Lahiri2, Li Wearn Koh3, Stanley Angkodjojo4, Andrew Yu Keat Khor5, James Jiaqi Liu6, Stephanie Wong7 and Siaw Ing Yeo6, 1National University of Singapore, Singapore, Singapore, 2National University Hospital, Singapore, Singapore, 3Tan Tock Seng Hospital, Braddell Heights, Singapore, 4Sengkang General Hospital / Singhealth, Singapore, Singapore, 5Changi General Hospital, Singapore, Singapore, 6Singapore General Hospital, Singapore, Singapore, 7Tan Tock Seng Hospital, Singapore, Singapore

    Background/Purpose: To determine the association of body mass index (BMI) with incident COVID-19 infection in patients with inflammatory arthritis (IA) using biologic disease-modifying anti-rheumatic drugs…
  • Abstract Number: 2164 • ACR Convergence 2023

    Real-world Persistence of Initial Targeted Therapy Strategy in Monotherapy versus Combination Therapy in Patients with Rheumatoid Arthritis, Psoriatic Arthritis, and Ankylosing Spondylitis

    Carlos Sánchez-Piedra1, Lorena Expósito2, PALOMA VELA3, Manuel José Moreno Ramos4, Cristina Campos5, Cristina Bohorquez6, Jerusalem Calvo7, Zulema Plaza8, Marta Domínguez9 and Jose Federico Diaz-Gonzalez10, 1Health Technology Assessment Agency (AETS), Instituto de Salud Carlos III, Madrid, Spain, 2Rheumatology Unit, Hospital Universitario de Canarias, San Cristóbal de La Laguna, Spain, 3Rheumatology, Hospital General Universitario Alicante, Alicante, Spain, 4Rheumatology Department Hospital Virgen de la Arrixaca, El Palmar Murcia, Spain, 5Rheumatology Unit, Hospital General Universitario de Valencia, Valencia, Spain, 6Rheumatology Unit, Hospital Universitario Príncipe de Asturias, Alcalá de Henares, Spain, 7Reina Sofia University Hospital, Córdoba, Spain, 8Universidad Autónoma de Madrid, Madrid, Spain, 9Sociedad Española de Reumatología, Madrid, Spain, 10Hospital Universitario de Canarias, La Laguna, Spain

    Background/Purpose: Clinical practice guidelines, based on information from clinical trials, provide different recommendations for the use of combination therapies for the treatment of rheumatoid arthritis…
  • Abstract Number: 2245 • ACR Convergence 2023

    Drug Survival of Risankizumab vs Other Biologics After 13 Months of Treatment Among Patients with PsA in the Multicountry Postmarketing Observational VALUE Study

    Lars Erik1, Kim A Papp2, Andrew Östör3, Vassilis Stakias4, Tshepiso Madihlaba4, Ralph Lippe5, Ran Liu4 and Diamant Thaçi6, 1Bispebjerg-Frederiksberg Hospital, Vedbæk, Denmark, 2Alliance Clinical Research and Probity Medical Research, Waterloo, and University of Toronto, Toronto, ON, Canada, 3Monash University & Emeritus Research; Australian National University, Melbourne, Australia, 4AbbVie, Inc., North Chicago, IL, 5AbbVie Deutschland GmbH & Co. KG, Wiesbaden, Germany, 6Institute and Comprehensive Center for Inflammation Medicine, University of Lübeck, Lübeck, Germany

    Background/Purpose: Risankizumab (RZB) is an optimized IL-23 inhibitor (IL-23i) currently approved for the treatment of plaque psoriasis (PsO), PsA, and Crohn's disease. In a post…
  • Abstract Number: 2482 • ACR Convergence 2023

    Preinflammatory Mesenchymal (PRIME) Cell Signature Genes Enrichment Predicts Treatment Response and Joint Prognosis in Rheumatoid Arthritis

    Takayuki Fujii1, Dana Orange2, Caryn Hale2, Koichi Murata1, Hideo Onizawa1, Akira Onishi1, Masao Tanaka3, Akio Morinobu4 and Shuichi Matsuda5, 1Department of Advanced Medicine for Rheumatic Diseases, Graduate School of Medicine, Kyoto University, Kyoto, Japan, 2Rockefeller University, New York, NY, 3Graduate School of Medicine, Kyoto University, Kyoto, Japan, 4Department of Rheumatology and Clinical Immunology, Graduate School of Medicine, Kyoto University, Kyoto, Japan, 5Department of Orthopaedic Surgery, Graduate School of Medicine, Kyoto University, Kyoto, Japan

    Background/Purpose: This study aimed to determine predictors of treatment response and radiographic progression following the initiation of biological disease-modifying antirheumatic medications (bDMARDs) in patients with…
  • Abstract Number: 032 • 2023 Pediatric Rheumatology Symposium

    From Bedside to Bench and Back: Discovery of a Novel Missense Variant in NLRP3 Causing Atypical Cryopyrin-Associated Periodic Syndromes with Hearing Loss as the Primary Presentation, Responsive to Anti-IL1 Therapy

    Merav Birk-Bachar1, Hadar Cohen2, Yoel Levinsky3, rotem tal4, Gil Amarilyo5, Meirav Sokolov6, Efrat Sofrin-Drucker7, Naama Orenstein7, Gabriel Lidzbarsky7, Liora Kornreich8, Eyal Raveh6, Nesya Kropach-Gilad7, Motti Gerlic2 and Liora Harel9, 1Pediatric Rheumatology Unit, Schneider Children's Medical Center of Israel, Petach Tikva, Israel, 2Sackler Faculty of Medicine, Immunology Department, Tel Aviv University, Tel Aviv, Israel, 3Schneider Children's Medical Center of Israel, Tel Aviv University, Petach Tikva, Israel, 4Schneider Children's Medical Center of Israel, Petach Tikva, Israel, 5Schneider Children's Medical Center of Israel, Petach Tikva, Israel, 6Pediatric Ear Nose and Throat Unit Unit, Schneider Children's Medical Center of Israel, Petach Tikva, Israel, 7Recanati Genetic Institute, Rabin Medical Center-Beilinson Hospital, Petach Tikva, Israel, 8Pediatric Imaging Unit, Schneider Children's Medical Center of Israel, Petach Tikva, Israel, 9Scheiders Children Medical Center of Israel, Petah-Tiqva, Israel

    Background/Purpose: Cryopyrin-associated periodic syndromes (CAPS) are a spectrum of rare autoinflammatory diseases caused by gain-of-function mutations inthe NLRP3 gene. These mutations cause inflammasome hyperactivity and…
  • Abstract Number: 073 • 2023 Pediatric Rheumatology Symposium

    Golimumab Therapy in Children with Chronic Recurrent Multifocal Osteomyelitis: A Case Series Reviewing Safety and Efficacy

    Claire Yang1, Natalie Rosenwasser2, Xing Wang2, Zheng Xu2, Joshua Scheck2, Ramesh Iyer3 and Yongdong (Dan) Zhao3, 1University of Washington School of Medicine, Seattle, WA, 2Seattle Children's Hospital, seattle, WA, 3University of Washington, Seattle, WA

    Background/Purpose: Chronic Recurrent Multifocal Osteomyelitis (CRMO) is an autoinflammatory bone disease requiring immunosuppressive therapy in half of patients. Monoclonal Tumor Necrosis Factor inhibitors (TNFi) are…
  • Abstract Number: 109 • 2023 Pediatric Rheumatology Symposium

    Long-term Safety of Biologics versus Conventional Synthetic Treatments in Systemic Juvenile Idiopathic Arthritis Patients

    Ana Isabel Rebollo-Giménez1, Luca Carlini2, Yulia Vyzhga3, Silvia Rosina4, Ekaterina Alexeeva5, Charlotte Myrup6, Silvia Magni Manzoni7, Maria Trachana8, Valda Stanevicha9, Constantin Ailioaie10, Elena Tsitsami11, Alexis-Virgil Cochino12, Chiara Pallotti13, Silvia Scala13, Angela Pistorio14, Sebastiaan Vastert15, Joost F. Swart16 and Nicolino Ruperto17, 1IRCCS Istituto Giannina Gaslini, UOC Reumatologia e Malattie Infiammatorie, Genova, Italy, 2IRCCS Istituto Giannina Gaslini, UOC Reumatologia e Malattie Autoinfiammatorie, Genova, Italy, 3IRCCS Istituto Giannina Gaslini, UOC Reumatologia e Malattia Infiammatorie, Genova, Italy, 4IRCCS Istituto Giannina Gaslini, Genova, Italy, 5Federal State Autonomous Institution “National Medical Research Center of Children's Health”, Ministry of Health of the Russian Federation, Moscow, Russia, 6Rigshospitalet, Pediatric rheumatology unit 4272, Copenhagem, Denmark, 7IRCCS Ospedale Pediatrico Bambino Gesù, Division of Rheumatology, Roma, Italy, 8Hippokration General Hospital, Thessaloniki University School of Medicine, First Department of pediatrics, Pediatric Immunology and Rheumatology Referral Center, Thessaloniki, Greece, 9Riga Stradins University, Children University Hospital, Riga, Latvia, 10Alexandru Ioan Cuza University of Iasi, Iasi, Romania, 11Aghia Sophia Childrens Hospital, First Department of Pediatrics, University of Athens Medical School, Athens, Greece, 12Institute for Mother and Child Care, Pediatrics, Bucharest, Romania, 13IRCCS Istituto Giannina Gaslini, U.O.C. Pediatric and Rheumatology Clinic, PRINTO, Genova, Italy, 14IRCCS Istituto Giannina Gaslini, Direzione Scientifica, Genova, Italy, 15Wilhelmina Children’s Hospital, Department of Pediatric Immunology and Rheumatology, Utrecht, The Netherlands, Utrecht, Netherlands, 16Wilhelmina Children’s Hospital, Department of Pediatric Immunology and Rheumatology, Utrecht, Netherlands, 17IRCCS Istituto Giannina Gaslini, UOSID Centro Trial, PRINTO, Genova, Italy

    Background/Purpose: The better understanding of systemic Juvenile Idiopathic Arthritis (sJIA) pathogenesis and availability of new drugs, such as biologic disease-modifying anti-rheumatic drugs (bDMARDs) specifically dedicated…
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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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