Updates are available Correction dated 2025-05-05
Click to view Correction: https://doi.org/10.1007/s40744-025-00761-x
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Authors
Mease, Philip J. https://orcid.org/0000-0002-6620-0457
Merola, Joseph F. https://orcid.org/0000-0001-6514-4353
Tanaka, Yoshiya https://orcid.org/0000-0002-0807-7139
Gossec, Laure https://orcid.org/0000-0002-4528-310X
McInnes, Iain B. https://orcid.org/0000-0002-6462-4280
Ritchlin, Christopher T. https://orcid.org/0000-0002-2602-1219
Landewé, Robert B. M. https://orcid.org/0000-0002-0577-6620
Asahina, Akihiko
Ink, Barbara
Heinrichs, Andrea
Bajracharya, Rajan
Shende, Vishvesh
Coarse, Jason
Coates, Laura C. https://orcid.org/0000-0002-4756-663X
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Documents that mention this clinical trial
POS0231 SUSTAINED EFFICACY AND SAFETY OF BIMEKIZUMAB IN PATIENTS WITH ACTIVE PSORIATIC ARTHRITIS AND PRIOR INADEQUATE RESPONSE TO TUMOUR NECROSIS FACTOR INHIBITORS: RESULTS FROM THE PHASE 3 BE COMPLETE STUDY AND ITS OPEN-LABEL EXTENSION UP TO 1 YEAR
https://doi.org/10.1136/annrheumdis-2023-eular.1306
Safety and Efficacy of Bimekizumab in Patients with Psoriatic Arthritis: 2-Year Results from Two Phase 3 Studies
https://doi.org/10.1007/s40744-024-00708-8
Long-term safety of bimekizumab in adult patients with axial spondyloarthritis or psoriatic arthritis: pooled results from integrated phase IIb/III clinical studies
https://doi.org/10.1136/rmdopen-2024-005026
Bimekizumab treatment in patients with active psoriatic arthritis and prior inadequate response to tumour necrosis factor inhibitors: 52-week safety and efficacy from the phase III BE COMPLETE study and its open-label extension BE VITAL
https://doi.org/10.1136/rmdopen-2023-003855
POS0961 BIMEKIZUMAB MAINTAINED EFFICACY RESPONSES THROUGH 52 WEEKS IN PATIENTS WITH ACTIVE PSORIATIC ARTHRITIS: RESULTS FROM TWO PHASE 3 STUDIES
https://doi.org/10.1136/annrheumdis-2024-eular.1239
Bimekizumab provided rapid improvements in patient-reported symptoms and health-related quality of life in patients with active psoriatic arthritis: pooled 16-week results from two phase 3 studies
https://doi.org/10.1136/rmdopen-2024-004464
Bimekizumab treatment in biologic DMARD-naïve patients with active psoriatic arthritis: 52-week efficacy and safety results from the phase III, randomised, placebo-controlled, active reference BE OPTIMAL study
https://doi.org/10.1136/ard-2023-224431
AB1099 SUSTAINED EFFICACY OF BIMEKIZUMAB TREATMENT ASSESSED USING COMPOSITE DISEASE ACTIVITY MEASURES IN PATIENTS WITH PSORIATIC ARTHRITIS AND PRIOR INADEQUATE RESPONSE OR INTOLERANCE TO TUMOUR NECROSIS FACTOR INHIBITORS: RESULTS FROM THE PHASE 3 BE COMPLETE STUDY AND ITS OPEN LABEL EXTENSION UP TO 1 YEAR
https://doi.org/10.1136/annrheumdis-2023-eular.1671
POS0969 BIMEKIZUMAB-TREATED PATIENTS WITH ACTIVE PSORIATIC ARTHRITIS SHOWED SUSTAINED ACHIEVEMENT OF MINIMAL DISEASE ACTIVITY AND REMISSION: UP TO 2-YEAR RESULTS FROM TWO PHASE 3 STUDIES
https://doi.org/10.1136/annrheumdis-2024-eular.2557
Comparative Effectiveness of Bimekizumab and Secukinumab in Patients with Psoriatic Arthritis at 52 Weeks Using a Matching-Adjusted Indirect Comparison
https://doi.org/10.1007/s40744-024-00652-7
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Funding
Funding for this research was provided by:
UCB Pharma
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Article History
Received: 16 June 2024
Accepted: 26 July 2024
First Online: 31 August 2024
Change Date: 1 May 2025
Change Type: Update
Change Details: The original online version of this article was revised to correct Table 2 and Supplementary material 2.
Change Date: 5 May 2025
Change Type: Correction
Change Details: A Correction to this paper has been published:
Change Details: https://doi.org/10.1007/s40744-025-00761-x
Declarations
:
: Philip J. Mease: Received research grants from AbbVie, Acelyrin, Amgen, BMS, Eli Lilly, Janssen, Novartis, Pfizer and UCB Pharma; consulting fees from AbbVie, Acelyrin, Aclaris, Alumis, Amgen, BMS, Boehringer Ingelheim, Eli Lilly, Inmagene, Janssen, Moonlake Pharma, Novartis, Pfizer, Takeda, UCB Pharma and Ventyx; speakers bureau fees from AbbVie, Amgen, Eli Lilly, Janssen, Novartis, Pfizer and UCB Pharma; data safety and advisory board for Genascence. Joseph F. Merola: Is a consultant and/or investigator for AbbVie, Amgen, AstraZeneca, Biogen, Boehringer Ingelheim, Bristol-Myers Squibb, Dermavant, Eli Lilly, Incyte, Janssen, LEO Pharma, MoonLake Immunotherapeutics, Novartis, Pfizer, Sanofi-Regeneron, Sun Pharma and UCB Pharma. Joseph F. Merola’s current affiliation is “Department of Dermatology and Department of Medicine, Division of Rheumatology, UT Southwestern Medical Center, Dallas, Texas, USA”. Yoshiya Tanaka: Speaker fees and/or honoraria from: AbbVie, Asahi-kasei, Astellas, AstraZeneca, Behringer-Ingelheim, Chugai, Daiichi-Sankyo, Eisai, Eli Lilly, Gilead, GlaxoSmithKline, Pfizer, Taisho, UCB Pharma; received grants from: Behringer-Ingelheim, Chugai, Taisho. Yoshiya Tanaka is an Editorial Board member of Rheumatology & Therapy. Yoshiya Tanaka was not involved in the selection of peer reviewers for the manuscript nor any of the subsequent editorial decisions. Laure Gossec: Grants or contracts from AbbVie, Biogen, Eli Lilly, Novartis and UCB Pharma; consulting fees from AbbVie, BMS, Celltrion, Janssen, Novartis, Pfizer and UCB Pharma; honoraria for lectures from AbbVie, Amgen, BMS, Celltrion, Janssen, Eli Lilly, MSD, Novartis, Pfizer, Stada and UCB Pharma; has received support for attending meetings and/or travel from MSD, Novartis, Pfizer; has received medical writing support from AbbVie, Amgen, Galapagos, Janssen, Pfizer and UCB Pharma. Membership on an entity’s Board of Directors or advisory committees: EULAR Treasurer. Iain B. McInnes: Consulting fees and honoraria from AbbVie, AstraZeneca, BMS, Boehringer Ingelheim, Cabaletta, Causeway Therapeutics, Celgene, Evelo, Janssen, Eli Lilly, Moonlake Immunotherapeutics, Novartis and UCB Pharma; Research support from BMS, Boehringer Ingelheim, Celgene, Janssen, Novartis, and UCB Pharma. Christopher T. Ritchlin: Research for AbbVie; consultant for Amgen, AbbVie, BMS, Eli Lilly, Janssen, MoonLake, Novartis, Pfizer, Solarea and UCB Pharma. Robert B. M. Landewé: Consultancy fees from AbbVie, AstraZeneca, BMS, Novartis, Pfizer, Eli Lilly, and UCB Pharma; research grants from AbbVie, Pfizer, Novartis, and UCB Pharma; owner of Rheumatology Consultancy BV, an AMS company under Dutch law. Akihiko Asahina: Honoraria and/or research grants from AbbVie, Amgen, Bristol Myers Squibb, Boehringer Ingelheim, Eisai, Eli Lilly, Janssen, Kyowa Kirin, LEO Pharma, Maruho, Mitsubishi Tanabe Pharma, Novartis, Pfizer, Sun Pharma, Taiho Pharma, Torii Pharmaceutical Co., and UCB Pharma. Barbara Ink: Employee of UCB Pharma, shareholder of AbbVie, GSK and UCB Pharma. Andrea Heinrichs, Vishvesh Shende: Employees of UCB Pharma. Rajan Bajracharya, Jason Coarse: Employees and shareholders of UCB Pharma. Laura C. Coates: Grants/research support from AbbVie, Amgen, Celgene, Eli Lilly, Gilead, Janssen, Novartis, Pfizer and UCB Pharma; consultant for AbbVie, Amgen, BMS, Boehringer Ingelheim, Celgene, Domain, Eli Lilly, Galapagos, Gilead, Janssen, Moonlake Immunotherapeutics, Novartis, Pfizer, and UCB Pharma; speaking fees from AbbVie, Amgen, Biogen, Celgene, Eli Lilly, Galapagos, Gilead, GSK, Janssen, medac, Novartis, Pfizer, and UCB Pharma. Laura C. Coates is an Editorial Board member of Rheumatology & Therapy. Laura C. Coates was not involved in the selection of peer reviewers for the manuscript nor any of the subsequent editorial decisions.
: Studies were conducted in accordance with the Declaration of Helsinki and the International Conference on Harmonization guidance for Good Clinical Practice. Ethical approval was obtained from the relevant institutional review boards at participating sites, and all patients provided written informed consent in accordance with local requirements.
: All the results presented in this article are in aggregate form, and no personally identifiable information was used for this study.
