ACR Meeting Abstracts

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Abstracts tagged "Biologicals"

  • Abstract Number: 0555 • ACR Convergence 2020

    Utilization and Adherence Among Infliximab Biosimilar Initiators in a U.S. National Commercial Insurance Database

    Sujith Sarvesh1, Joseph Alanaeme1, Jeffrey R Curtis2 and Huifeng Yun2, 1University of Alabama at Birmingham, BIrmingham, AL, 2Division of Clinical Immunology and Rheumatology, University of Alabama at Birmingham, Birmingham, AL

    Background/Purpose: Infliximab Biosimilar, the first biosimilar to infliximab, was approved for multiple indications in the U.S. in 2016. Since the utilization of biosimilar in the…
  • Abstract Number: 0798 • ACR Convergence 2020

    A Randomized, Double-blind Phase 3 Study Comparing the Efficacy, Safety and Immunogenicity of PF-06410293 (Abrilada™), an Adalimumab (ADL) Biosimilar, and Reference ADL (Humira®) in Patients with Moderate to Severe Active RA: Results from Weeks 52-92

    Roy Fleischmann1, Daniel Alvarez2, Amy Bock3, Carol Cronenberger4, Ivana Vranic5, Wuyan Zhang6 and Rieke Alten7, 1Southwestern Medical Center, Metroplex Clinical Research Center, Dallas, TX, 2Pfizer, Collegeville, PA, 3Pfizer, Cambridge, MA, 4Pfizer, Collegeville, 5Pfizer, Tadworth, United Kingdom, 6Pfizer, New York, 7Schlosspark-Klinik, Universitätsmedizin, Berlin, Germany

    Background/Purpose: To evaluate the long-term safety, immunogenicity (IG), and efficacy of the adalimumab (ADL) biosimilar, PF-06410293 (ADL-PF), in patients (pts) with moderate to severe active…
  • Abstract Number: 0830 • ACR Convergence 2020

    Discontinuation Rate of Tofacitinib Is Similar When Compared to TNF Inhibitors in Rheumatoid Arthritis Patients: Real World Results from a Rheumatoid Arthritis Cohort

    Mohammad Movahedi1, Angela Cesta2, Xiuying Li3, Edward C Keystone4 and Claire Bombardier5, 1Toronto General Hospital Research Institute, University Health Network, Toronto, ON, Canada, 2Toronto General Hospital Research Institute, Toronto, ON, Canada, 3Toronto General Hospital Research Institute, Toronto, Canada, 4Mount Sinai Hospital, Toronto, ON, Canada, 5Institute for Work and Health, Toronto, ON, Canada

    Background/Purpose: Tofacitinib (TOFA) is an oral, small molecule drug used for rheumatoid arthritis (RA) treatment and is prescribed alone or with methotrexate (MTX). TOFA can…
  • Abstract Number: 0908 • ACR Convergence 2020

    Guselkumab Efficacy in Adult Patients with Active Psoriatic Arthritis by Baseline Demographic and Disease Characteristics: Pooled Results of Two Phase 3, Randomized, Placebo-Controlled Studies

    Atul Deodhar1, Philip Mease2, Wolf-Henning Boehncke3, John Tesser4, Elena Schiopu5, Soumya Chakravarty6, Alexa Kollmeier7, Elizabeth Hsia8, Xie Xu9, May Shawi10, Yusang Jiang11, Shihong Sheng11, Prasheen Agarwal11, Joseph Merola12, Iain McInnes13 and Christopher Ritchlin14, 1Oregon Health & Science University, Portland, OR, 2Seattle Rheumatology Associates, P.L.L.C., Seattle, WA, 3Geneva University Hospitals, Geneva, Switzerland, 4Arizona Arthritis & Rheumatology Associates, Phoenix, AZ, 5Michigan Medicine, Ann Arbor, MI, 6Janssen Scientific Affairs, LLC, Horsham, PA, USA and Drexel University College of Medicine, Horsham, PA, 7Janssen Research & Development, LLC, La Jolla, CA, 8Janssen Research & Development, LLC and University of Pennsylvania Medical Center, Spring House, PA, 9Janssen Research & Development, LLC, San Marcos, CA, 10Janssen Global Services, LLC, Toronto, ON, Canada, 11Janssen Research & Development, LLC, Spring House, PA, 12Brigham and Women's Hospital, Harvard Medical School, Newton, MA, 13Institute of Infection, Immunity, and Inflammation, University of Glasgow, Glasgow, United Kingdom, 14Department of Medicine, University of Rochester Medical Center, Rochester, NY

    Background/Purpose: Guselkumab (GUS), a human monoclonal antibody targeting the IL-23p19-subunit, has shown consistent efficacy in psoriasis pts regardless of body weight/body mass index (BMI).1 GUS…
  • Abstract Number: 1237 • ACR Convergence 2020

    Pain and Other Patient-Reported Outcomes in Patients with Rheumatoid Arthritis Who Did or Did Not Achieve Treatment Response Based on Improvement in Swollen Joints in Tocilizumab Clinical Trials

    Anthony Sebba1, Jian Han2 and Shalini V. Mohan2, 1Arthritis Associates, Palm Harbor, Tampa, FL, 2Genentech, South San Francisco, CA

    Background/Purpose: Recent data suggest that rheumatoid arthritis (RA) pain may be noninflammatory and inflammatory, and improvement in pain scores and other patient-reported outcomes (PROs) may…
  • Abstract Number: 1428 • ACR Convergence 2020

    The Efficacy and Safety of Tocilizumab in Patients with Giant Cell Arteritis: A Systematic Review and Meta-Analysis

    Matthew J. Koster1, Kenneth Warrington1, Jian Han2 and Shalini V. Mohan2, 1Mayo Clinic, Rochester, MN, 2Genentech, South San Francisco, CA

    Background/Purpose: Tocilizumab (TCZ) has been proven to be safe and effective for the treatment of giant cell arteritis (GCA) in 2 randomized controlled trials; however,…
  • Abstract Number: 1827 • ACR Convergence 2020

    Flare Reduction and Oral Corticosteroid Taper in Patients with Active SLE Treated with Anifrolumab in 2 Phase 3 Trials

    Richard Furie1, Eric Morand2, Anca Askanase3, Ed Vital4, Joan Merrill5, Rubana Kalyani6, Gabriel Abreu7, Lilia Pineda6 and Raj Tummala6, 1Zucker School of Medicine at Hofstra/Northwell, Great Neck, 2Medicine, School of Clinical Sciences at Monash Health, Monash University, Melbourne, Australia, 3Columbia University College of Physicians and Surgeons, New York, 4University of Leeds; NIHR Leeds Biomedical Research Centre, Leeds Teaching Hospitals NHS Trust, Leeds, United Kingdom, 5Oklahoma Medical Research Foundation, Oklahoma City, 6BioPharmaceuticals R&D, AstraZeneca, Gaithersburg, 7BioPharmaceuticals R&D, AstraZeneca, Gothenburg, Sweden

    Background/Purpose: Objectives of long-term SLE management are not only to reduce disease activity, but also to prevent flares and minimize exposure to oral corticosteroids (OCS),…
  • Abstract Number: 0058 • ACR Convergence 2020

    Drug Retention and Discontinuation of Biological DMARDs and Novel Small Molecules: Data from the Singapore National Biologics Registry

    Li Wearn Koh1, Man Hua Aw2, Preeti Dhanasekaran3, Rosa Lim Mui San1, Stephanie Wong4, Xanthe Chua5, Wei Joo Choy1, Manjari Lahiri6 and Siaw Ing Yeo2, 1Tan Tock Seng Hospital, Singapore, Singapore, 2Singapore General Hospital, Singapore, Singapore, 3National University of Singapore, Singapore, Singapore, 4Clinical Research and Innovation Office, Tan Tock Seng Hospital Singapore, Singapore, Singapore, 5Tan Tock Seng Hospital, Singapore, Singapore, Singapore, 6National University Hospital, Singapore, Singapore

    Background/Purpose: To describe drug retention rate and reasons for discontinuation of biological disease modifying anti-rheumatic drugs ( bDMARD) and novel small molecules in patients from…
  • Abstract Number: 0232 • ACR Convergence 2020

    Safety and Effectiveness of Tocilizumab in Patients with Renal Insufficiency in the Non-interventional Study ICHIBAN

    Christof Specker1, Martin Aringer2, Gerd Burmester3, Johannes Gerlach4, Michael Hofmann5, Herbert Kellner6, Frank Moosig7, Hans-Peter Tony8 and Gerhard Fliedner9, 1Clinic Essen-Mitte, Essen, Germany, 2Rheumatology, Medicine III, University Medical Center & Faculty of Medicine, TU Dresden, Dresden, Germany, Dresden, Germany, 3Charité University Hospital Berlin, Berlin, Germany, 4Roche Pharma AG, Grenzach-Wyhlen, Germany, 5Chugai, Frankfurt am Main, Germany, 6Rheumatology and Gastroenterology Specialty Practice, Munich, Germany, 7Rheumatology Center Schleswig-Holstein Middle, Neumünster, Germany, 8Rheumatology/Clinical Immunology, Department of Internal Medicine II, Würzburg, Germany, 9Rheumatology Practice, Onsabrück, Germany

    Background/Purpose: RA increases a patient’s systemic inflammatory burden, which has been associated with development of chronic kidney disease (CKD), especially in patients with comorbid hypertension,…
  • Abstract Number: 0359 • ACR Convergence 2020

    Clinical Characteristics of Psoriatic Arthritis Patients with Physician-Identified Spondylitis, According to HLA-B27 Status: An Analysis from the Corrona Psoriatic Arthritis/Spondyloarthritis Registry

    Philip Mease1, Soumya Chakravarty2, Robert McLean3, Taylor Blachley3, Toana Kawashima4, Iris Lin5, Jonathan Uy6, Arthur Kavanaugh7 and Alexis Ogdie8, 1Seattle Rheumatology Associates, P.L.L.C., Seattle, WA, 2Janssen Scientific Affairs, LLC, Horsham, PA, USA and Drexel University College of Medicine, Horsham, PA, 3Corrona, LLC, Waltham, MA, 4Corrona, LLC, Waltham, 5Janssen Immunology Global Commercial Strategy Organization, Horsham, 6Janssen Scientific Affairs, LLC, Horsham, 7UC San Diego Health System, San Diego, CA, 8Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA

    Background/Purpose: Axial disease in psoriatic arthritis (PsA) has been reported to occur in anywhere from 25% to 75% of PsA patients (pts). It can be…
  • Abstract Number: 0556 • ACR Convergence 2020

    Recent Use, Missed Doses and Discontinuation of Infliximab in New-users: Comparisons of Biosimilar and Originator Exposures

    Cristiano Moura1, Jeffrey R Curtis2, Denis Choquette3, Gilles Boire4, Vivian Bykerk5, Carter Thorne6, Walter Maksymowych7, Peter Lakatos1, Larry Svenson8, Laura Targownik5, Waqqas Afif1 and Sasha Bernatsky9, 1McGill University, Montreal, Canada, 2Division of Clinical Immunology and Rheumatology, University of Alabama at Birmingham, Birmingham, AL, 3Institut de Rhumatologie de Montréal, Montreal, Canada, 4Universite de Sherbrooke, Sherbrooke, Canada, 5University of Toronto, Toronto, Canada, 6Ontario Rheumatology Association, Aurora, Canada, 7University of Alberta, Edmonton, AB, Canada, 8University of Alberta, Edmonton, Canada, 9The Research Institute of the McGill University Health Centre, Montreal, ON, Canada

    Background/Purpose: Biosimilar infliximab offers a potentially lower‐cost treatment option compared to its bio‐originator. However, uptake of biosimilars in general in North America has been slow.…
  • Abstract Number: 0799 • ACR Convergence 2020

    Effectiveness of Electronic Drug Monitoring Feedback in Order to Increase Adherence in RA Patients Starting with a Biological DMARD

    Renske Hebing1, Wouter Bos1, Mike Nurmohamed2 and Bart van den Bemt3, 1Amsterdam Rheumatology and Immunology Center | Reade, Amsterdam, Netherlands, 2Amsterdam Rheumatology and immunology Center, location Reade and Amsterdam UMC, VU medical center, Amsterdam, Netherlands, 3Sint Maartenskliniek, Nijmegen, Netherlands

    Background/Purpose: Medication non-adherence in rheumatoid arthritis (RA) is associated with disease flares, increased disability and increased costs. Electronic Monitoring Feedback (EMF) to improve adherence has…
  • Abstract Number: 0849 • ACR Convergence 2020

    Herpes Zoster Events with Anifrolumab in Patients with Active SLE: An Integrated Analysis of Phase 2 and Phase 3 Trials

    Joan Merrill1, Kenneth Kalunian2, Richard Furie3, Kevin Winthrop4, Patricia Primakov5, Lilia Pineda6, Gabriel Abreu7 and Raj Tummala6, 1Oklahoma Medical Research Foundation, Oklahoma City, 2School of Health Sciences, University of California, La Jolla, 3Zucker School of Medicine at Hofstra/Northwell, Great Neck, NY, 4Oregon Health & Science University, Portland, OR, 5BioPharmaceuticals R&D, AstraZeneca, Gaithersburg, MD, 6BioPharmaceuticals R&D, AstraZeneca, Gaithersburg, 7BioPharmaceuticals R&D, AstraZeneca, Gothenburg, Sweden

    Background/Purpose: In the phase 2 MUSE and phase 3 TULIP-1 and TULIP-2 trials, treatment with anifrolumab, a monoclonal antibody to the type I interferon receptor,…
  • Abstract Number: 0909 • ACR Convergence 2020

    Residual Disease Activity in Psoriatic Arthritis Patients Treated with Secukinumab and Adalimumab Who Achieved Remission or Low Disease Activity: Results from a Phase 3b, Randomized, Double-blinded, Active-controlled, Head-to-head Study

    Iain McInnes1, Philip Mease2, Dafna Gladman3, Laura Coates4, Peter Nash5, Alexis Ogdie6, Frank Behrens7, Philippe Goupille8, Arthur Kavanaugh9, Ruvie Martin10, Erhard Quebe-Fehling11 and Corine Gaillez11, 1Institute of Infection, Immunity, and Inflammation, University of Glasgow, Glasgow, United Kingdom, 2Seattle Rheumatology Associates, P.L.L.C., Seattle, WA, 3Krembil Research Institute, Toronto Western Hospital, Toronto, ON, Canada, 4University of Oxford, Oxford, United Kingdom, 5School of Medicine Griffith University, Brisbane, Queensland, Australia, 6University of Pennsylvania, Philadelphia, PA, 7CIRI/Rheumatology & Fraunhofer IME, Research Division Translational Medicine and Pharmacology, Goethe University Hospital, Frankfurt, Hessen, Germany, 8CHU Tours, department of rheumatology, Tours, France, 9Division of Rheumatology, Allergy, & Immunology, University of California San Diego Medical School, San Diego, CA, 10Novartis Pharmaceuticals Corporation, East Hanover, NJ, 11Novartis Pharma AG, Basel, Switzerland

    Background/Purpose: Recent EULAR recommendations propose that treatment of psoriatic arthritis (PsA) should seek remission (REM) or alternatively low disease activity (LDA) by regular disease activity…
  • Abstract Number: 1335 • ACR Convergence 2020

    Smoking, but Not Use of Complementary and Alternative Medicine Predicts Residual Functional Disability in Patients with Inflammatory Arthritis on Biologic Disease Modifying Anti-Rheumatic Drugs: Results from the Singapore National Biologics Register

    Dominic Seet1, Li Wearn Koh2, Preeti Dhanasekaran3, Man Hua Aw4, Rosa Lim Mui San2, Siaw Ing Yeo4 and Manjari Lahiri1, 1National University Hospital, Singapore, Singapore, 2Tan Tock Seng Hospital, Singapore, Singapore, 3National University of Singapore, Singapore, Singapore, 4Singapore General Hospital, Singapore, Singapore

    Background/Purpose: To describe the demographic and clinical characteristics of patients with inflammatory arthritis (IA) initiating biologic disease modifying anti-rheumatic drugs (bDMARD) who use complementary 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.

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.).

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