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: 2255

Bimekizumab versus Secukinumab for the Treatment of Nail Psoriasis in Patients with Moderate to Severe Plaque Psoriasis: Results from the BE RADIANT Phase 3b Trial

Kilian Eyerich1, Alice B. Gottlieb2, Stefano Piaserico3, Stefan Beissert4, Melinda Gooderham5, Brian Kirby6, Nicola Tilt7, Cynthia Madden8, Susanne Wiegratz9, Dirk de Cuyper10, Joseph F. Merola11 and Boni Elewski12, 1Department of Dermatology, Medical Center, University of Freiburg, Freiburg, Germany, 2Icahn School of Medicine at Mount Sinai, New York, NY, 3Dermatology Unit, Department of Medicine, Università di Padova, Padova, Italy, 4Department of Dermatology, University Hospital Carl Gustav Carus, TU Dresden, Dresden, Germany, 5SKiN Centre for Dermatology, Probity Medical Research, Peterborough, ON, Canada, and Queen’s University, Kingston, ON, Canada, 6Elm Park and the Charles Institute, St Vincent's University Hospital, University College Dublin, Dublin, Ireland, 7UCB Pharma, Slough, United Kingdom, 8UCB Pharma, Morrisville, NC, 9UCB Pharma, Monheim am Rhein, Germany, 10UCB Pharma, Brussels, Belgium, 11Brigham and Women's Hospital and Harvard Medical School, Boston, MA, 12Department of Dermatology, University Hospitals of Cleveland, Case Western Reserve University, Cleveland, OH

Meeting: ACR Convergence 2023

Keywords: clinical trial, Dermatology

  • Tweet
  • Email
  • Print
Session Information

Date: Tuesday, November 14, 2023

Title: (2227–2256) Spondyloarthritis Including Psoriatic Arthritis – Treatment: SpA Poster III

Session Type: Poster Session C

Session Time: 9:00AM-11:00AM

Background/Purpose: Psoriatic lesions in highly visible areas, including the nails, disproportionately affect patients’ health‑related quality of life.[1] Here, we compare the efficacy of bimekizumab (BKZ) vs secukinumab (SEC) through 48 weeks (wks) for the treatment of nail psoriasis in patients with moderate to severe plaque psoriasis who had moderate to severe nail involvement at baseline.

Methods: In BE RADIANT, patients were randomized to BKZ 320mg every 4 wks (Q4W) or SEC 300mg weekly to Wk4 then Q4W. From Wk16, BKZ-randomized patients received BKZ Q4W or Q8W.[2] In this analysis, BKZ Q4W/Q4W and Q4W/Q8W were combined (BKZ Total). Modified Nail Psoriasis Severity Index (mNAPSI; total fingernail on a 0–130 scale) and mNAPSI sub-scores from Wks16–48 among patients with baseline mNAPSI >10 were assessed. Missing data were imputed as non-response (NRI).

Results: In total, 116 BKZ-treated and 99 SEC-treated patients had baseline mNAPSI >10; 37.1% and 40.4% achieved mNAPSI≤2 at Wk16; 75.0% and 59.6% achieved mNAPSI≤2 at Wk48. From Wks16–48, mNAPSI=0 (clear) response rates increased from 26.7% to 70.7% (BKZ), and 33.3% to 53.5% (SEC). 101 BKZ-treated and 86 SEC-treated patients had both baseline mNAPSI >10 and baseline nail pitting >0; 36.6% and 41.9% achieved nail pitting=0 (clear) at Wk16; 78.2% and 59.3% achieved nail pitting=0 at Wk48. 69 BKZ-treated and 56 SEC-treated patients had both baseline mNAPSI >10 and baseline nail plate crumbling >0; 65.2% and 69.6% achieved nail plate crumbling=0 (clear) at Wk16; 85.5% and 75.0% achieved nail plate crumbling=0 at Wk48. 59 BKZ-treated and 58 SEC‑treated patients had both baseline mNAPSI >10 and baseline leukonychia >0; 69.5% and 70.7% achieved leukonychia=0 (clear) at Wk16; 79.7% and 69.0% achieved leukonychia=0 at Wk48.

Conclusion: From Wks16–48, BKZ-treated patients showed numerically greater improvements in nail psoriasis than SEC‑treated patients, including complete nail clearance.

Funding: This study was funded by UCB Pharma. Medical writing provided by Costello Medical and funded by UCB Pharma.

References: 1. Augustin M et al. Br J Dermatol 2019;181(2):358–65; 2. Reich K et al. N Engl J Med 2021;385(2):142–52, NCT03536884. Abstract previously submitted to AAD 2023.


Disclosures: K. Eyerich: AbbVie, 12, Speaker and/or advisor for:, Almirall, 12, Speaker and/or advisor for:, Boehringer Ingelheim, 12, Speaker and/or advisor for:, Bristol Myers Squibb, 12, Speaker and/or advisor for:, Eli Lilly, 12, Speaker and/or advisor for:, Janssen, 12, Speaker and/or advisor for:, LEO Pharma, 12, Speaker and/or advisor for:, Novartis, 12, Speaker and/or advisor for:, Pfizer, 12, Speaker and/or advisor for:, Sanofi, 12, Speaker and/or advisor for:, UCB Pharma, 12, Speaker and/or advisor for:; A. Gottlieb: Amgen, 1, 2, AnaptysBio, 1, 2, 5, Avotres Therapeutics, 1, 2, Boehringer Ingelheim, 1, 2, Bristol Myers Squibb, 1, 2, 5, Dice Therapeutics, 1, 2, Eli Lilly, 1, 2, Janssen, 1, 2, MoonLake Immunotherapeutics, 5, Novartis, 1, 2, 5, Sanofi, 1, 2, UCB Pharma, 1, 2, 5, XBiotech, 1, 2; S. Piaserico: AbbVie, 2, 6, Almirall, 2, 6, Celgene, 2, 6, Eli Lilly, 2, 6, Janssen, 2, 6, LEO Pharma, 2, 6, Merck, 2, 6, Novartis, 2, 6, Pfizer, 2, 6, Sandoz, 2, 5, UCB Pharma, 2, 6; S. Beissert: AbbVie, 6, Actelion, 6, Amgen, 6, Bristol Myers Squibb, 6, Celgene, 6, Eli Lilly, 6, Galderma, 6, GSK, 6, Janssen, 6, LEO Pharma, 6, Menlo Therapeutics, 6, MSD, 6, Novartis, 6, Pfizer, 6, Roche Posay, 6, UCB Pharma, 6; M. Gooderham: AbbVie, 12, Investigator, speaker, consultant or advisory board member for:, Akros, 12, Investigator, speaker, consultant or advisory board member for:, Amgen, 12, Investigator, speaker, consultant or advisory board member for:, AnaptysBio, 12, Investigator, speaker, consultant or advisory board member for:, Arcutis, 12, Investigator, speaker, consultant or advisory board member for:, Aslan, 12, Investigator, speaker, consultant or advisory board member for:, Bausch Health, 12, Investigator, speaker, consultant or advisory board member for:, Boehringer Ingelheim, 12, Investigator, speaker, consultant or advisory board member for:, Bristol Myers Squibb, 12, Investigator, speaker, consultant or advisory board member for:, Celgene, 12, Investigator, speaker, consultant or advisory board member for:, Dermavant, 12, Investigator, speaker, consultant or advisory board member for:, Dermira, 12, Investigator, speaker, consultant or advisory board member for:, Eli Lilly, 12, Investigator, speaker, consultant or advisory board member for:, Galderma, 12, Investigator, speaker, consultant or advisory board member for:, GSK, 12, Investigator, speaker, consultant or advisory board member for:, Incyte, 12, Investigator, speaker, consultant or advisory board member for:, Janssen, 12, Investigator, speaker, consultant or advisory board member for:, Kyowa Kirin, 12, Investigator, speaker, consultant or advisory board member for:, MedImmune, 12, Investigator, speaker, consultant or advisory board member for:, Meiji, 12, Investigator, speaker, consultant or advisory board member for:, Merck, 12, Investigator, speaker, consultant or advisory board member for:, Moonlake Immunotherapeutics, 12, Investigator, speaker, consultant or advisory board member for:, Nimbus, 12, Investigator, speaker, consultant or advisory board member for:, Novartis, 12, Investigator, speaker, consultant or advisory board member for:, Pfizer, 12, Investigator, speaker, consultant or advisory board member for:, Regeneron, 12, Investigator, speaker, consultant or advisory board member for:, Reistone, 12, Investigator, speaker, consultant or advisory board member for:, Sanofi-Genzyme, 12, Investigator, speaker, consultant or advisory board member for:, Sun Pharma, 12, Investigator, speaker, consultant or advisory board member for:, UCB Pharma, 12, Investigator, speaker, consultant or advisory board member for:; B. Kirby: AbbVie, 1, 2, 6, 12, Received research support from or has been a principal investigator (clinical trials) for:, Almirall, 1, 2, 6, 12, Received research support from or has been a principal investigator (clinical trials) for:, Celgene, 1, 2, 6, Eli Lilly, 1, 6, Janssen, 1, 2, 6, 12, Received research support from or has been a principal investigator (clinical trials) for:, Merck, 2, 12, Received research support from or has been a principal investigator (clinical trials) for:, Moonlake Immunotherapeutics, 1, 2, 6, 12, Received research support from or has been a principal investigator (clinical trials) for:, Novartis, 1, 2, 6, 12, Received research support from or has been a principal investigator (clinical trials) for:, Pfizer, 1, 2, 6, 12, Received research support from or has been a principal investigator (clinical trials) for:, UCB Pharma, 1, 2, 6, 12, Received research support from or has been a principal investigator (clinical trials) for:; N. Tilt: UCB Pharma, 3, 11; C. Madden: UCB Pharma, 3, 11; S. Wiegratz: UCB Pharma, 3, 11; D. de Cuyper: UCB Pharma, 3, 11; J. Merola: AbbVie, 12, Consultant and/or investigator, Amgen, 2, Biogen, 12, Consultant and/or investigator, Bristol Myers Squibb, 2, Dermavant, 12, Consultant and/or investigator, Eli Lilly, 12, Consultant and/or investigator, Janssen, 12, Consultant and/or investigator, LEO Pharma, 12, Consultant and/or investigator, Novartis, 12, Consultant and/or investigator, Pfizer, 12, Consultant and/or investigator, Regeneron, 12, Consultant and/or investigator, Sanofi, 12, Consultant and/or investigator, Sun Pharmaceuticals, 12, Consultant and/or investigator, UCB Pharma, 12, Consultant and/or investigator; B. Elewski: AbbVie/Abbott, 12, Received research support as funding to Case Western Reserve University from:, AnaptysBio, 12, Received research support as funding to Case Western Reserve University from:, Arcutis, 2, Boehringer Ingelheim, 2, 12, Received research support as funding to Case Western Reserve University from:, Bristol Myers Squibb, 2, 12, Received research support as funding to Case Western Reserve University from:, Celgene, 2, 12, Received research support as funding to Case Western Reserve University from:, Eli Lilly, 2, 12, Received research support as funding to Case Western Reserve University from:, Incyte, 12, Received research support as funding to Case Western Reserve University from:, LEO Pharma, 2, 12, Received research support as funding to Case Western Reserve University from:, Menlo, 2, 12, Received research support as funding to Case Western Reserve University from:, Novartis, 2, 12, Received research support as funding to Case Western Reserve University from:, Pfizer, 2, 12, Received research support as funding to Case Western Reserve University from:, Regeneron, 12, Received research support as funding to Case Western Reserve University from:, Sun Pharma, 2, 12, Received research support as funding to Case Western Reserve University from:, UCB Pharma, 2, Valeant, 2, 12, Received research support as funding to Case Western Reserve University from:, Vanda, 12, Received research support as funding to Case Western Reserve University from:, Verrica, 2.

To cite this abstract in AMA style:

Eyerich K, Gottlieb A, Piaserico S, Beissert S, Gooderham M, Kirby B, Tilt N, Madden C, Wiegratz S, de Cuyper D, Merola J, Elewski B. Bimekizumab versus Secukinumab for the Treatment of Nail Psoriasis in Patients with Moderate to Severe Plaque Psoriasis: Results from the BE RADIANT Phase 3b Trial [abstract]. Arthritis Rheumatol. 2023; 75 (suppl 9). https://acrabstracts.org/abstract/bimekizumab-versus-secukinumab-for-the-treatment-of-nail-psoriasis-in-patients-with-moderate-to-severe-plaque-psoriasis-results-from-the-be-radiant-phase-3b-trial/. Accessed .
  • Tweet
  • Email
  • Print

« Back to ACR Convergence 2023

ACR Meeting Abstracts - https://acrabstracts.org/abstract/bimekizumab-versus-secukinumab-for-the-treatment-of-nail-psoriasis-in-patients-with-moderate-to-severe-plaque-psoriasis-results-from-the-be-radiant-phase-3b-trial/

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