ACR Meeting Abstracts

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  • Abstract Number: 1501 • 2014 ACR/ARHP Annual Meeting

    Immunogenicity Assessment of PF-06438179, a Potential Biosimilar to Infliximab, in Healthy Volunteers

    Chandrasekhar Udata1, Donghua Yin2, Chun-hua Cai3, Stephanie Salts4, Steven Y. Hua4, Muhammad I. Rehman5 and Xu Meng2, 1Clinical Pharmacology, Pfizer Inc., San Diego, CA, 2Clinical Pharmacology/Pharmacometrics, Pfizer Inc., San Diego, CA, 3Pfizer Inc., Groton, CT, 4Pfizer Inc., San Diego, CA, 5Pfizer Inc., Cambridge, MA

    Background/Purpose: PF-06438179, a proposed biosimilar to infliximab, was evaluated for immunogenicity in a phase 1 pharmacokinetic (PK) similarity study. Methods: In this double-blind trial (NCT01844804),…
  • Abstract Number: 1500 • 2014 ACR/ARHP Annual Meeting

    Preclinical and Clinical Characterization of MK-8457, a Selective Spleen Tyrosine Kinase and Zeta-Chain-Associated Protein Kinase 70 Inhibitor, in Normotensive and Hypertensive Cardiovascular Models

    Hani Houshyar1, Alan Bass2, Judith Boice3, Michael Ellis4, Patrick Fanelli5, Tomoko Freshwater6, Jane Guo7, Kimberly Hoagland5, Janet Kerr5, Alan Northrup4, Mathew Maddess8, Richard Miller9, Marcella Ruddy10, Stella Vincent11, Jayanthi Wolf5, Haoling Weng3, Gloria Zingaro5 and Gene Marcantonio3, 133 Avenue Louis Pasteur, Merck & Co., Boston, MA, 2Safety Assessment, Merck & Co., Boston, MA, 3Merck & Co., Whitehouse Station, NJ, 4Medicinal Chemistry, Merck & Co., Boston, MA, 5Merck & Co., West Point, PA, 6PPDM Early Stage, Merck & Co., Rahway, NJ, 7Immunology, Merck & Co., Boston, MA, 8Discovery Process Chemistry, Merck & Co., Boston, MA, 9Biochemistry & Biophysics, Merck & Co., Boston, MA, 10Merck & Co., Boston, MA, 11PPDM Preclinical ADME, Merck & Co., Boston, MA

    Background/Purpose:  Spleen Tyrosine Kinase (SYK) and Zeta-chain-associated protein kinase 70 (ZAP70) are non-receptor protein kinases that bind phosophorylated receptor tyrosine-based activation motifs, critical in immune…
  • Abstract Number: 1499 • 2014 ACR/ARHP Annual Meeting

    Characterization of ABT-494, a Second Generation Jak1 Selective Inhibitor

    Candace Graff1, Annette Schwartz1, Jeffrey Voss2, Neil Wishart3, Lisa Olson1, Jonathon George3, Deborah Hyland3 and Heidi Camp4, 1AbbVie Inc, AbbVie Bioresearch Center, Worcester, MA, 2Immunology, AbbVie Pharmaceuticals, Worcester, MA, 3Abbvie Pharmaceuticals, worcester, MA, 41101 Oak Street, Abbvie, Winnetka, IL

    Background/Purpose  Jak kinase blockade can effectively manage rheumatoid arthritis (RA) and in some cases achieve remission. However, first generation Jak inhibitors have not met expectations…
  • Abstract Number: 1498 • 2014 ACR/ARHP Annual Meeting

    ALX-0061, an Anti-IL-6R Nanobody® for use in Rheumatoid Arthritis, Demonstrates a Different in Vitro Profile As Compared to Tocilizumab

    Maarten Van Roy1, Ariella Van De Sompel2, Kristi De Smet2, Jasper Jacobs2, Tinneke Denayer2 and Hans Ulrichts3, 1Department of Pharmacology, Ablynx N.V., Zwijnaarde, Belgium, 2Ablynx N.V., Zwijnaarde, Belgium, 3Pharmacology, Ablynx N.V., Zwijnaarde, Belgium

    Background/Purpose Interleukin-6 (IL-6) is a pleiotropic cytokine inducing a wide range of biological activities via its receptor, which can either be soluble (sIL-6R) or membrane-bound…
  • Abstract Number: 1497 • 2014 ACR/ARHP Annual Meeting

    Efficacy and Safety of Iguratimod for Rheumatoid Arthritis

    Tsuneo Kondo1, Akiko Shibata1, Ryota Sakai1, Kentaro Chino1, Ayumi Okuyama1, Hirofumi Takei1 and Koichi Amano2, 1Rheumatology and Clinical Immunology, Saitama Medical Center, Saitama Medical University, Kawagoe, Japan, 2Saitama Medical Center, Saitama Medical University, Kawagoe, 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: 1496 • 2014 ACR/ARHP Annual Meeting

    Exposure-Response Analysis for Mavrilimumab Phase2b Study in RA Patients with Informative Dropout

    Chi-Yuan Wu1, Denise Jin1, Alex Godwood2, David Close3, Lorin Roskos4 and Bing Wang1, 1Clinical Pharmacology and DMPK, Medimmune, Mountain View, CA, 2Clinical Biostatics and Data Management, MedImmune Ltd, Cambridge, United Kingdom, 3Clinical Development, MedImmune Ltd, Cambridge, United Kingdom, 4One MedImmune Way, Medimmune, Gaithersburg, MD

    Background/Purpose: Mavrilimumab is a recombinant human monoclonal antibody which neutralizes granulocyte-macrophage colony stimulating factor (GM-CSF) activity by selectively binding to the alpha subunit of its…
  • Abstract Number: 1495 • 2014 ACR/ARHP Annual Meeting

    Preclinical and Clinical Phase I Profile of MK-8457, a Selective Spleen Tyrosine Kinase and Zeta-Chain-Associated Protein Kinase 70 Inhibitor, Developed for the Treatment of Rheumatoid Arthritis

    Gene Marcantonio1, Alan Bass2, Gretchen Baltus3, Judith Boice1, Hongmin Chen4, Michael Crackower5, Jeroen Elassaiss-Schaap6, Michael Ellis7, Tomoko Freshwater8, Francois Gervais9, Jane Guo10, Sammy Kim9, Lily Moy5, Alan Northrup7, Jie Zhang-Hoover4, Mathew Maddess11, Richard Miller12, Marcella Ruddy5, Stella Vincent13, Haoling Weng1 and Hani Houshyar14, 1Merck & Co., Whitehouse Station, NJ, 2Safety Assessment, Merck & Co., Boston, MA, 3Immunomodulatory Regulators, Merck & Co., Boston, MA, 4Pharmacology, Merck & Co., Boston, MA, 5Merck & Co., Boston, MA, 6Clinical PK-PD, Merck & Co., Oss, Netherlands, 7Medicinal Chemistry, Merck & Co., Boston, MA, 8PPDM Early Stage, Merck & Co., Rahway, NJ, 9Cell Pathways and Proteins, Merck & Co., Boston, MA, 10Immunology, Merck & Co., Boston, MA, 11Discovery Process Chemistry, Merck & Co., Boston, MA, 12Biochemistry & Biophysics, Merck & Co., Boston, MA, 13PPDM Preclinical ADME, Merck & Co., Boston, MA, 1433 Avenue Louis Pasteur, Merck & Co., Boston, MA

    Background/Purpose: Spleen tyrosine kinase (SYK) is a potential target for treatment of several diseases including rheumatoid arthritis.  SYK is a member of the Zeta-chain-associated protein…
  • Abstract Number: 1494 • 2014 ACR/ARHP Annual Meeting

    Treatment of Rheumatoid Arthritis Patients with the JAK1-Selective Inhibitor GLPG0634 Reverses an Arthritis-Specific Blood Gene Signature to Healthy State

    Mate Ongenaert1, Sonia Dupont2, Béatrice Vayssière2, Reginald Brys1, Luc Van Rompaey1, Christel Menet1 and René Galien2, 1Galapagos NV, Mechelen, Belgium, 2Galapagos SASU, Romainville, France

    Background/Purpose The 4 Janus kinases (JAK1, JAK2, JAK3 and TYK2) are cytoplasmic tyrosine kinases that mediate intracellular signaling of cytokines (e.g. certain interleukins and interferons)…
  • Abstract Number: 1493 • 2014 ACR/ARHP Annual Meeting

    A Phase 1 Study of FPA008, an Anti-Colony Stimulating Factor 1 Receptor (anti-CSF1R) Antibody in Healthy Volunteers and Subjects with Rheumatoid Arthritis (RA): Preliminary Results

    Julie Hambleton1, Lei Zhou1, Seema Rogers1, Sjoerd van Marle2, Thijs van Iersel2, James Zanghi1, Emma Masteller1, Kevin Baker1 and Brian Wong1, 1Five Prime Therapeutics, South San Francisco, CA, 2PRA Health Sciences, Groningen, Netherlands

    Background/Purpose Activation of CSF1R via IL34 or CSF1 results in activation, differentiation, and survival of monocytes, macrophages and osteoclasts.  CSF1R activation produces inflammatory cytokines responsible…
  • Abstract Number: 1491 • 2014 ACR/ARHP Annual Meeting

    Discovery and Characterization of COVA322, a Clinical Stage Bispecific TNF/IL-17A Inhibitor for the Treatment of Inflammatory Diseases

    Dragan Grabulovski, Michela Silacci, Wibke Lembke, Wenjuan Zha, Richard Woods, Roger Santimaria, Julian Bertschinger and Mathias Locher, Covagen AG, Schlieren, Switzerland

    Background/Purpose: Biologics such as TNF inhibitors have revolutionized the treatment of inflammatory diseases including rheumatoid arthritis (RA), psoriasis and psoriatic arthritis. However, recent data suggest that…
  • Abstract Number: 1490 • 2014 ACR/ARHP Annual Meeting

    Can Tumor Necrosis Factor Inhibitors Protect Rheumatoid Arthritis Patients from Osteoporosis? Impact of Tumor Necrosis Factor Inhibitors on Bone Mineral Density and Bone Remodeling Markers

    Anaïz Nutz1, Yohan Duny2, Thomas Barnetche3, Jacques Morel4, Bernard Combe5 and Claire Daien6, 1Rheumatology, Hopital Lapeyronie, Montpellier, France, 2INSERM, Montpellier, France, 3Department of rheumatology, Bordeau, France, 4Department of Rheumatology, Hôpital Lapeyronie, Montpellier, France, 5Immuno-Rhumatologie, Hôpital Lapeyronie, Montpellier, France, 6Hopital Lapeyronie, Montpellier, France

    Background/Purpose Rheumatoid Arthritis (RA) is a chronic inflammatory disease characterized by joint and bone destruction. Loss of bone in RA is not only localized in…
  • Abstract Number: 1489 • 2014 ACR/ARHP Annual Meeting

    Influences of Disease Activity at the Initiation of Iguratimod, a Small Molecule Antirheumatic Drug, on Efficacy of Iguratimod in Patients with Rheumatoid Arthritis –a Multicenter Registry Study-

    Yuji Hirano1, Toshihisa Kojima2, Yasuhide Kanayama3, Shinya Hirabara1, Nobunori Takahashi2, Atsushi Kaneko4 and Naoki Ishiguro2, 1Rheumatology, Toyohashi Municipal Hospital, Toyohashi, Japan, 2Orthopaedic Surgery and Rheumatology, Nagoya University Graduate School of Medicine, Nagoya, Japan, 3Orthopedic Surgery and Rheumatology, Toyota Kosei Hospital, Toyota, Japan, 4Orthopedic Surgery and Rheumatology, Nagoya Medical Center, Nagoya, Japan

    Background/Purpose: Iguratimod (IGU), known as T-614, is a small-molecule antirheumatic drug developed in Japan and used in Japanese clinical practice since June in 2012. IGU…
  • Abstract Number: 1487 • 2014 ACR/ARHP Annual Meeting

    A Phase 1 Dose-Ranging Repeated-Dose Trial of Parenteral Staphylococcal Protein A (PRTX-100) in Patients with Active Rheumatoid Arthritis on Methotrexate or Leflunamide Therapy

    Craig Wiesenhutter1,2, Rakesh Patel3, John Lavery4, Nighat Tahir5,6, Lydie Hazan7, Alan Kivitz8, Elizabeth Bretton9 and Jeffrey Kaine10, 1University of Washington School of Medicine, Seattle, WA, 2Coeur d’Alene Arthritis Clinic, Coeur d’Alene, ID, 3PMG Research of Salisbury, Salisbury, NC, 4Allen Arthritis and Allergy, Allen, TX, 5Community Hospital of Anderson and Madison County, Inc., Anderson, IN, 6Community Rheumatology of Anderson, Anderson, IN, 7Axis Clinical Trials, Los Angeles, CA, 8Altoona Center for Clinical Research, Duncansville, PA, 9Albuquerque Clinical Trials, Albuquerque, NM, 10Sarasota Arthritis Center, Sarasota, FL

    Background/Purpose Staphylococcal protein A (SpA) binds with high affinity to the Fc region of human immunoglobulin G and also to the Fab framework region of…
  • Abstract Number: 1492 • 2014 ACR/ARHP Annual Meeting

    Safety and Tolerability of NNC0114­0006, an Anti-IL-21 Monoclonal Antibody, at Multiple s.c. Dose Levels in Patients with Rheumatoid Arthritis

    Frank Wagner1, Birte Skrumsager2 and Sergey Fitilev3, 1Charité Research Org GmbH, Berlin, Germany, 2Novo Nordisk A/S, Søborg, Denmark, 3Department of Clinical Pharmacology, Municipal Clinic #2, Moscow, Russia

    Background/Purpose A phase 1, randomised, double-blind, placebo-controlled, dose-escalation trial was conducted to assess the safety and tolerability of the anti-IL-21-antibody NNC0114-0006, in patients with active…
  • Abstract Number: 1472 • 2014 ACR/ARHP Annual Meeting

    Synovial Fluid from Rheumatoid Arthritis Patients Modulates the Immunophenotype and Viability of Monocytes

    Maria Sole Chimenti, Alberto Bergamini, Eleonora Baffari, Eleonora Ballanti, Alessia Musto, Paola Conigliaro and Roberto Perricone, Rheumatology, allergology and clinical immunology, Department of "Medicina dei Sistemi", University of Rome "Tor Vergata", Rome, Italy

    Background/Purpose Rheumatoid arthritis (RA) is a chronic systemic autoimmune disease characterized by infiltration of the synovium by inflammatory cells that destroys the cartilage and the…
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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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