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Abstracts tagged "Randomized Trial"

  • Abstract Number: 1485 • ACR Convergence 2020

    LNA043, a Novel Cartilage Regenerative Treatment for Osteoarthritis: Results from a First-In-Human Trial in Patients with Knee Osteoarthritis

    Celeste Scotti1, Joseph Gimbel2, Didier Laurent1, Aviv Madar3, Thomas Peters1, Yunyu Zhang3, Florine Polus1, Michael Beste3, Igor Vostiar1, Subhajit Choudhury4, Nicole Gerwin1, Jörg Goldhahn5, Matthias Schieker1 and Ronenn Roubenoff1, 1Novartis Institutes for BioMedical Research, Basel, Switzerland, 2Arizona Research Center, Phoenix, 3Novartis Institutes for BioMedical Research, Cambridge, 4Biostatistics & Pharmacometrics, Novartis Healthcare Pvt. Ltd., Hyderabad, India, 5Department of Health Sciences and Technology, ETH Zürich, Zurich, Switzerland

    Background/Purpose:LNA043 is a modified human angiopoietin-like 3 (ANGPTL3) protein identified in a phenotypic screen for inducers of chondrogenesis and cartilage repair. The primary objective of…
  • Abstract Number: 0200 • ACR Convergence 2020

    Predictors of Durable Clinical Response to Tofacitinib 11 Mg Once Daily with or Without Methotrexate in Patients with Rheumatoid Arthritis: Post Hoc Analysis of Data from a Phase 3b/4 Methotrexate Withdrawal Study

    Kunihiro Yamaoka1, Stanley B Cohen2, Naonobu Sugiyama3, Harry Shi4, Jose L Rivas5, Annette Diehl4 and Josef Smolen6, 1Kitasato University School of Medicine, Sagamihara, Kanagawa, Japan, 2Metroplex Clinical Research Center, Dallas, TX, 3Pfizer Japan Inc, Tokyo, Japan, 4Pfizer Inc, Collegeville, PA, 5Pfizer SLU, Madrid, Spain, 6Division of Rheumatology, Department of Medicine III, Medical University of Vienna, Vienna, Austria

    Background/Purpose: ORAL Shift, a global Phase 3b/4 non-inferiority study, demonstrated sustained efficacy/safety of tofacitinib modified-release (MR) 11 mg QD following MTX withdrawal in patients (pts)…
  • Abstract Number: 0962 • ACR Convergence 2020

    Efficacy of Clomipramine for Chronic Lumbar Radicular Pain a Randomized Clinical Trial

    Saloua Afilal1, Safaa Fellous1, Ilham Aachari1, Redouane Abouqal2, Ihsane Hmamouchi3, Nada Alami1, Latifa Tahiri1, Hanan Rkain1, Najia Hajjaj-Hassouni4 and Fadoua Allali1, 1Rheumatology B Department, El Ayachi Hospital, Faculty of Medicine and Pharmacy of Rabat, Mohammed V University, Rabat, Morocco., Rabat, Morocco, 2Laboratory of Biostatistics, Clinical Research and Epidemiology (LBRCE), Faculty of Medicine and Pharmacy, Mohammed V University, Rabat, Morocco., Rabat, Morocco, 3Temara Hospital, Laboratory of Biostatistics, Clinical Research and Epidemiology (LBRCE), Faculty of Medicine and Pharmacy, Mohammed V University, Rabat, Morocco, Rabat, Morocco, 4Health Sciences College, International University of Rabat (UIR), Rabat, Morocco

    Background/Purpose: Lumbar radicular pain is the most common chronic neuropathic pain syndrome. Antidepressants are highly recommended for neuropathic pain, but there is no evidence for…
  • Abstract Number: 1486 • ACR Convergence 2020

    Long-term Efficacy and Safety of Intra-articular Sprifermin in Patients with Knee Osteoarthritis: Results from the 5-Year Forward Study

    Felix Eckstein1, Marc Hochberg2, Hans Guehring3, Flavie Moreau4, Victor Ona4, Asger Bihlet5, Inger Byrjalsen5, Jeppe Andersen5, Benjamin Daelken3, Oliver Guenther3, Christoph Ladel3, Martin Michaelis3 and Philip G Conaghan6, 1Paracelsus Medical University, Salzburg, Austria, 2University of Maryland School of Medicine, Baltimore, MD, 3Merck KGaA, Darmstadt, Germany, 4EMD Serono (a business of Merck KGaA, Darmstadt, Germany), Billerica, MA, 5Nordic Bioscience, Herlev, Denmark, 6Leeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds, and National Institute for Health Research Leeds Biomedical Research Centre, Leeds, United Kingdom

    Background/Purpose: The 5-year Phase II FORWARD study assessed the efficacy and safety of the potential disease-modifying osteoarthritis drug (DMOAD) sprifermin (recombinant human fibroblast growth factor…
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Embargo Policy

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.).

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].

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