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

Abstract Number: 0728

Intra-articular Canakinumab (anti-interleukin-1β) for Treatment of Symptomatic Knee Osteoarthritis: A Randomized, Double-blind, Placebo and Naproxen-controlled Phase II Study

Philip Conaghan1, Xavier Chevalier2, Linda Mindeholm3, Ursula Schramm3, Jens Praestgaard3, Abdelkader Seroutou3, Ronenn Roubenoff3 and Matthias Schieker3, 1Leeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds, Leeds, United Kingdom, 2Henri Mondor University Hospital and Paris University XII, UPEC, Créteil, France, Créteil, France, 3Novartis Institutes for Biomedical Research, Basel, Switzerland, Basel, Switzerland

Meeting: ACR Convergence 2021

Keywords: C-reactive protein (CRP), Inflammation, Interleukins, Nonsteroidal antiinflammatory drugs (NSAIDs), Osteoarthritis

  • Tweet
  • Email
  • Print
Session Information

Date: Sunday, November 7, 2021

Title: Osteoarthritis – Clinical Poster II (0723–0738)

Session Type: Poster Session B

Session Time: 8:30AM-10:30AM

Background/Purpose: Knee osteoarthritis (OA) is a common musculoskeletal disease associated with pain and functional impairment. There are few effective therapies, often limited by side-effects.1 This phase II study investigated the efficacy, safety, and pharmacokinetics of canakinumab, an anti-interleukin-1β antibody, in patients (pts) with knee OA (NCT01160822).

Methods: The study had a single placebo (PBO)-controlled ascending dose period assessing the safety of intra-articular (i.a.) canakinumab, and an 18-week randomized, double-blind, double-dummy PBO and naproxen-controlled period. Pts (N = 136) with symptomatic knee OA (VAS pain ≥40, Kellgren/Lawrence [K/L] grade 2 or 3) were enrolled to receive a single i.a. injection of canakinumab 600 mg or matched PBO at baseline (BL), and naproxen 500 mg twice daily or matched PBO. Co-primary endpoints were change from BL in knee OA pain (VAS 0-100] at Day 4 and in Western Ontario and McMaster OA Index (WOMAC) pain (scale 0-20) at Day 29.

Results: Canakinumab i.a was generally safe and well tolerated and had a short resident time in the joint with an early detection (1 hour) in the circulation after i.a. injection. The co-primary efficacy endpoints were not met. The rapid and clinically significant decreases from BL in VAS pain and WOMAC pain scores were largely comparable between canakinumab, PBO and naproxen (Figure 1A). In a post hoc analysis of pts with BL elevated high sensitive C-reactive protein (hsCRP) levels (≥2 mg/L), canakinumab had a more pronounced inhibitory effect on pain than PBO or naproxen (-2.56 [-5.16; 0.04], P = 0.11; adjusted mean (90% CI) from a mixed-effect model repeated measures [MMRM]) at Day 57. Furthermore, this subpopulation showed a (-1.24 [-3.87; 1.39], P = 0.44) reduction of WOMAC pain at Day 85 compared to PBO or naproxen (Figure 1B).

Conclusion: The effect of canakinumab on pain in a population with knee OA was not different from PBO or naproxen. An effect of canakinumab on pain was observed in a subpopulation with elevated BL hsCRP levels. In addition to the data published previously on the CANTOS study2, these findings underscore the need to identify specific populations of pts with knee OA, who may benefit from anti-inflammatory treatment.

References: 1. Eymard F, Chevalier X. Rev Prat. 2019;69:515-9. 2. Schieker et al, Ann Intern Med. 2020;173:509-15.


Disclosures: P. Conaghan, AbbVie, 2, 6, BMS, 2, 6, Eli Lilly, 2, 6, Galapagos, 2, 6, Gilead, 2, 6, Novartis, 2, 6, Pfizer, 2, 6, AstraZeneca, 2, 6; X. Chevalier, Ibsa, 2, 5, 6, Sanofi, 2, Flexion therapics, 1, 2, magpharma, 1; L. Mindeholm, Novartis, 3, 12, Shareholder; U. Schramm, Novartis, 3, 12, Shareholder; J. Praestgaard, Novartis, 3; A. Seroutou, Novartis, 3; R. Roubenoff, Novartis, 3, 11; M. Schieker, Novartis, 3, 11.

To cite this abstract in AMA style:

Conaghan P, Chevalier X, Mindeholm L, Schramm U, Praestgaard J, Seroutou A, Roubenoff R, Schieker M. Intra-articular Canakinumab (anti-interleukin-1β) for Treatment of Symptomatic Knee Osteoarthritis: A Randomized, Double-blind, Placebo and Naproxen-controlled Phase II Study [abstract]. Arthritis Rheumatol. 2021; 73 (suppl 9). https://acrabstracts.org/abstract/intra-articular-canakinumab-anti-interleukin-1%ce%b2-for-treatment-of-symptomatic-knee-osteoarthritis-a-randomized-double-blind-placebo-and-naproxen-controlled-phase-ii-study/. Accessed .
  • Tweet
  • Email
  • Print

« Back to ACR Convergence 2021

ACR Meeting Abstracts - https://acrabstracts.org/abstract/intra-articular-canakinumab-anti-interleukin-1%ce%b2-for-treatment-of-symptomatic-knee-osteoarthritis-a-randomized-double-blind-placebo-and-naproxen-controlled-phase-ii-study/

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