ACR Meeting Abstracts

ACR Meeting Abstracts

  • Meetings
    • ACR Convergence 2024
    • ACR Convergence 2023
    • 2023 ACR/ARP PRSYM
    • ACR Convergence 2022
    • ACR Convergence 2021
    • ACR Convergence 2020
    • 2020 ACR/ARP PRSYM
    • 2019 ACR/ARP Annual Meeting
    • 2018-2009 Meetings
    • Download Abstracts
  • Keyword Index
  • Advanced Search
  • Your Favorites
    • Favorites
    • Login
    • View and print all favorites
    • Clear all your favorites
  • ACR Meetings

Abstracts tagged "pharmacokinetics and rheumatoid arthritis (RA)"

  • Abstract Number: 506 • 2017 ACR/ARHP Annual Meeting

    The Selective JAK1 Inhibitor Upadacitinib Has No Effect on Pharmacokinetics of the Hormonal Contraceptives Levonorgestrel and Ethinylestradiol

    Mohamed-Eslam F. Mohamed1, Sheryl Trueman1, Tian Feng2, Alan Friedman3 and Ahmed A. Othman2, 1Clinical Pharmacology and Pharmacometrics, AbbVie, North Chicago, IL, 2AbbVie, North Chicago, IL, 3AbbVie Inc., North Chicago, IL

    Background/Purpose: Upadacitinib is a selective JAK1 inhibitor being developed for the treatment of several inflammatory diseases, including rheumatoid arthritis (RA).  Upadacitinib showed favorable efficacy and…
  • Abstract Number: 519 • 2017 ACR/ARHP Annual Meeting

    Filgotinib, a Selective Janus Kinase 1 Inhibitor, Has No Effect on QT Interval in Healthy Subjects

    Kacey Anderson1, Hao Zheng2, Chohee Yun3, Ellen Kwan4, Ann Qin1, Florence Namour5, Brian P. Kearney1 and Yan Xin1, 1Clinical Pharmacology, Gilead Sciences, Inc., Foster City, CA, 2Gilead Sciences, Inc., Foster City, CA, 3Clinical Research, Gilead Sciences, Inc, Foster City, CA, 4Clinical Operations, Gilead Sciences, Inc, Foster City, CA, 5Galapagos NV, Romainville, France

    Background/Purpose: Filgotinib is a potent and selective Janus kinase 1 (JAK1) inhibitor being developed to treat inflammatory diseases. Safety pharmacology studies and Phase 1 studies…
  • Abstract Number: 646 • 2016 ACR/ARHP Annual Meeting

    Population Pharmacokinetics of ABT-122, an Immunoglobulin Targeting Both TNF-α and IL-17A: Analyses Across Phase 1 Studies in Healthy Volunteers and Phase 2 Studies in Subjects with Rheumatoid or Psoriatic Arthritis

    Amit Khatri and Ahmed A. Othman, AbbVie Inc., North Chicago, IL

    Background/Purpose: ABT-122 is a novel dual-variable domain immunoglobulin (DVD-IgTM), which specifically neutralizes both TNF alpha (TNFα) and interleukin-17A (IL-17). Drugs individually neutralizing TNFα or IL-17…
  • Abstract Number: 1594 • 2016 ACR/ARHP Annual Meeting

    First-in-Human Pharmacokinetics and Safety of Escalating Single- and Multiple-Doses of GS-9876, a Novel, Oral SYK Inhibitor, in Healthy Subjects

    Michael Dolton1, Franziska Matzkies2, Kevin Currie3, Julie Di Paolo4, Lu Wang3, Hao Zheng3, Srini Ramanathan3 and Jeffrey Silverman3, 1Clinical Pharmacology, Gilead Sciences, Inc, Foster City, CA, 2Gilead Sciences, Inc, Foster City, CO, 3Gilead Sciences, Inc, Foster City, CA, 4Biology, Gilead Sciences, Foster City, CA

    Background/Purpose: Spleen Tyrosine Kinase (SYK) mediates immunoreceptor signaling in a range of hematopoietic cells important for the initiation and progression of inflammatory diseases such as…
  • Abstract Number: 1604 • 2016 ACR/ARHP Annual Meeting

    a First-in-Human Study of CR6086, a New Potent EP4 Prostanoid Receptor Antagonist, Demonstrates Good Safety and Tolerability at Therapeutically Relevant Exposures

    Stefano Persiani1, Carla Manzotti1, Cristina Vitalini1, Giampaolo Giacovelli2, Federica Girolami1, Massimo D'Amato1, Gianfranco Caselli1 and Lucio C. Rovati2,3, 1Rottapharm Biotech, Monza, Italy, 2Clinical Research Department, Rottapharm Biotech, Monza, Italy, 3University of Milano Bicocca, Milano, Italy

    Background/Purpose: CR6086 is a potent and selective antagonist of the prostaglandin EP4 receptor. EP4 receptors have a role in T-cell differentiation and expansion, and thus…
  • Abstract Number: 1607 • 2016 ACR/ARHP Annual Meeting

    The Development of a New Anti–Interleukin 6 Blocker for Rheumatoid Arthritis Patients

    Alan Glicklich1, Paul Grayson1, Christophe Blanchetot2, Qing Zhou3 and Anke Kretz-Rommel1, 1Bird Rock Bio, Inc, La Jolla, CA, 2Argenx, Ghent, Belgium, 3Genor BioPharma, Shanghai, China

    Background/Purpose: While interleukin-6 (IL-6) blockade with monoclonal antibodies is an established, clinically validated mechanism for the treatment of rheumatoid arthritis (RA), the need for significant…
  • Abstract Number: 1629 • 2016 ACR/ARHP Annual Meeting

    Pharmacokinetics of ABT-494 with the Once-Daily Extended-Release Tablet Formulation Being Utilized in the Ongoing Rheumatoid Arthritis Phase 3 Trials

    Mohamed-Eslam Mohamed1, Jiewei Zeng2, In-Ho Song3 and Ahmed A. Othman3, 1Clinical Pharmacology and Pharmacometrics, AbbVie, North Chicago, IL, 2AbbVie, North Chicago, IL, 3AbbVie Inc., North Chicago, IL

    Background/Purpose: ABT-494 is a selective Janus Kinase 1 inhibitor. In two Phase 2b studies in subjects with rheumatoid arthritis, 6 mg and 12 mg twice-daily…
  • Abstract Number: 3014 • 2016 ACR/ARHP Annual Meeting

    Tapering of Adalimumab Based on Therapeutic Drug Monitoring in Rheumatoid Arthritis

    Merel J. l'Ami1, Anneke F. Marsman1, Charlotte LM Krieckaert1, Mike T. Nurmohamed2,3, Jill Ruwaard1, Ingrid M. Visman1, Eva L. Kneepkens1 and Gertjan Wolbink1,4, 1Rheumatology, Amsterdam Rheumatology and immunology Center, location Reade, Amsterdam, Netherlands, 2Rheumatology, Amsterdam Rheumatology and immunology Center, Location VU University Medical Center, Amsterdam, Netherlands, Amsterdam, Netherlands, 3Rheumatology, Amsterdam Rheumatology and immunology Center, location Reade, Amsterdam, Netherlands, Amsterdam, Netherlands, 4Immunopathology, Sanquin Research and Landsteiner Laboratory Academic Medical Center, Amsterdam, Netherlands

    Background/Purpose: Treatment with biologicals is based on the principle of ‘one size fits all’ without taking differences into account for dosing schemes, patients’ characteristics and…
  • Abstract Number: 2727 • 2015 ACR/ARHP Annual Meeting

    BI 695501, a Proposed Biosimilar for Adalimumab, Shows Bioequivalence to Adalimumab Reference Products in a Randomized, Double-Blind Phase I Trial in Healthy Subjects

    Christopher Wynne1, Magdalena Petkova2, Ferdinand Rombout3, Niklas Czeloth3, Mario Altendorfer3, Benjamin Lang4, Francois-Xavier Frapaise3 and Rod Ellis-Pegler5, 1Christchurch Clinical Studies Trust, Christchurch, New Zealand, 2SGS, CPU Antwerpen, Antwerp, Belgium, 3Boehringer Ingelheim, Ingelheim, Germany, 4Boehringer Ingelheim, Biberach an der Riss, Germany, 5Auckland Clinical Studies Limited, Auckland, New Zealand

    Background/Purpose: BI 695501 is a proposed adalimumab biosimilar currently in development and was evaluated for pharmacokinetic (PK) similarity to both US-licensed and EU-approved reference products.…
Advanced Search

Your Favorites

You can save and print a list of your favorite abstracts during your browser session by clicking the “Favorite” button at the bottom of any abstract. View your favorites »

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.).

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].

Wiley

  • Online Journal
  • Privacy Policy
  • Permissions Policies
  • Cookie Preferences

© Copyright 2025 American College of Rheumatology