UCB, a global biopharmaceutical company, today announced new data on its investigational IL-17A and IL-17F inhibitor, bimekizumab, and its TNF inhibitor, CIMZIA® (certolizumab pegol). Eleven abstracts are being presented at the ACR Convergence 2021 virtual congress on November 3-9, 2021, reinforcing UCB's ongoing commitment to developing treatments that address unmet patient needs.
UCB is investigating bimekizumab in psoriatic arthritis (PsA) and axial spondyloarthritis (axSpA), including ankylosing spondylitis (AS) and non-radiographic axial spondyloarthritis (nr-axSpA), among other therapy areas, as part of a robust clinical program. Bimekizumab is currently under review by the U.S. Food and Drug Administration (FDA) for the treatment of moderate to severe plaque psoriasis in adults, and its efficacy and safety have not been established for any indication in the U.S.
"We are pleased to have the opportunity to share data across our strong immunology clinical programs at ACR Convergence 2021 and beyond," said Jeffrey Stark, MD, Head of Immunology Medical Affairs U.S., UCB. "Our bimekizumab data support the selective inhibition of IL-17F in addition to IL-17A in the treatment of ankylosing spondylitis and psoriatic arthritis, and demonstrate the potential of bimekizumab to provide durable clinical responses over three years for people living with these severe, chronic conditions."
Bimekizumab Data Highlights
An oral presentation will highlight three-year bimekizumab data in AS from the Phase 2b BE AGILE study and its open-label extension (OLE).1 Data show the long-term safety profile of bimekizumab in patients with AS was in line with previous observations, and clinical outcomes were maintained and consistent over three years of treatment.1,2,3 In addition to the oral presentation, UCB is presenting two e-posters; one that will report three-year interim health-related quality of life data in patients with active AS from the Phase 2b BE AGILE study and its OLE, and a second that evaluates the impact of the COVID-19 pandemic on disease activity and health-related quality of life in patients from the BE AGILE OLE study.2,3
Two e-posters will also report bimekizumab data in active PsA from the Phase 2b dose-ranging study BE ACTIVE and its OLE.4,5 Data reported include the impact up to three years on patient reported outcome measures, and long-term efficacy and safety in the overall bimekizumab population and tumor necrosis factor inhibitor (TNFi)-naïve population.4,5
CIMZIA (certolizumab pegol) Data Highlights
UCB will also present six e-posters detailing CIMZIA data, including the first release of three-year results from the C-axSpAnd pivotal Phase 3 study evaluating the long-term safety and efficacy of CIMZIA in nr-axSpA.6,7,8,9,10,11 The analysis reports safety and clinical outcomes in nr-axSpA patients who entered the C-axSpAnd open-label safety follow-up extension (SFE) study. Data show CIMZIA improved signs and symptoms of nr-axSpA for up to three years, and there were no new safety signals.
Building on CIMZIA efficacy in nr-axSpA, a new analysis from this patient population in the C-OPTIMISE study shows that over a year of CIMZIA treatment, clinically relevant responses are achieved in MRI positive patients regardless of their C-reactive protein (CRP) levels. Two e-posters also demonstrate that achieving higher thresholds of disease control with CIMZIA helps reduce the burden on work productivity for people living with axSpA and PsA.7,11
Following is a guide to the UCB-sponsored data presentations:
Bimekizumab Oral Presentation
Bimekizumab Long-Term Safety and Efficacy in Patients with Ankylosing Spondylitis: Interim Results After 3 Years of Treatment in an Ongoing Phase 2b Study
L. S. Gensler, A. Deodhar, D. van der Heijde, D. Poddubnyy, A. J. Kivitz, M. Dougados, N. de Peyrecave, M. Oortgiesen, T. Vaux, C. Fleurinck, X. Baraliakos (Abstract #0491 – Saturday, Nov. 6; 2:45-2:55pm ET)
Bimekizumab Shows Sustained and Meaningful Long-Term Improvements in Health-Related Quality of Life in Ankylosing Spondylitis: Interim Results After 3 Years of Treatment in an Ongoing Phase 2b Study
A. Deodhar, M. Dougados, K. Gaffney, R. Sengupta, M. Magrey, N. de Peyrecave, M. Oortgiesen, T. Vaux, C. Fleurinck, V. Taieb, C. de la Loge, X. Baraliakos (Abstract #0922 – Sunday, Nov. 7; 8:30-10:30am ET)
Minimal Impact of the COVID-19 Pandemic on Patient-Reported Disease Activity and Health-Related Quality of Life in Patients with Ankylosing Spondylitis Receiving Bimekizumab: Post Hoc Analyses from a Phase 2b Study
P. C. Robinson, P. M. Machado, N. Haroon, L. S. Gensler, J. D. Reveille, V. Taieb, T. Vaux, C. Fleurinck, M. Oortgiesen, N. de Peyrecave, A. Deodhar (Abstract #0923 – Sunday, Nov. 7; 8:30-10:30am ET)
Bimekizumab in Patients with Psoriatic Arthritis: 3-Year Results for Overall and Tumor Necrosis Factor Inhibitor (TNFi)-Naïve Populations from a Phase 2b Open-Label Extension Study
P. J. Mease, A. Deodhar, J. F. Merola, I. B. McInnes, D. Assudani, R. Bajracharya, J. Coarse,6 B. Ink, G. Schett (Abstract #1338 – Monday, Nov. 8; 8:30-10:30am ET)
Sustained Improvement in Physical Function, Disease Impact and HealthRelated Quality of Life in Patients with Psoriatic Arthritis Treated with Bimekizumab: 3-Year Results from a Phase 2b Open-Label Extension Study
L. Gossec, A. Asahina, A. B. Gottlieb, L. C. Coates, B. Ink, D. Assudani, J. Coarse, S. Hellot, J. Eells, P. J. Mease (Abstract #1350 - Monday, Nov. 8; 8:30-10:30am ET)
Achievement of Stringent Thresholds of Disease Control is Associated with Reduced Burden on Work and Household Productivity in Patients with Axial Spondyloarthritis
M. Rudwaleit, P. M. Machado, L. S. Gensler, V. Taieb, N. de Peyrecave, B. Hoepken, D. van der Heijde (abstract #0362 – Saturday, Nov. 6; 8:30-10:30am ET)
Long-Term Safety and Efficacy of Certolizumab Pegol in Patients with Active Non–Radiographic Axial Spondyloarthritis: 3-Year Results from a Phase 3 Multicenter Study
D. van der Heijde, L. S. Gensler, W. P. Maksymowych, R. Landewé, M. Rudwaleit, L. Bauer, B,. Hoepken, T. Kumke, M. Kim, A. Deodhar (Abstract #0913 – Sunday, Nov. 7; 8:30-10:30am ET)
Response to Certolizumab Pegol in Patients with Non-Radiographic Axial Spondyloarthritis by Baseline C-Reactive Protein Cut-Offs: Post-Hoc Analysis from a Phase 3 Multicenter Study
P. C. Robinson, S. Hall, B. Hoepken, L. Bauer, E. Demas, M. Kim, A. Deodhar (Abstract #0914 – Sunday, Nov. 7; 8:30-10:30am ET)
Disease Activity and Inflammation in Axial Spondyloarthritis Patients Who Did Not Experience Flares Following Certolizumab Pegol Withdrawal, Dose Reduction or Dose Continuation
L. S. Gensler, X. Baraliakos, L. Bauer, B. Hoepken, T. Kumke, M. Kim, R. Landewé (Abstract #0916 – Sunday, Nov. 7; 8:30-10:30am ET)
Reduced Burden on Paid and Household Work Productivity with Stringent Thresholds of Disease Control: Further Results from Long-Term Certolizumab Pegol Treatment in Patients with Psoriatic Arthritis
W. Tillett, L. C. Coates, S. Kiri, V. Taieb, P. J. Mease (Abstract #1826 – Tuesday, Nov. 9; 8:30-10:30am ET)
Other UCB e-Posters:
Development of a Deep Learning Algorithm for the Detection of Sacroiliitis on MRI in Patients with Active Axial Spondyloarthritis
J. Nicolaes, P. M. Machado, X. Baraliakos, M. Santosh, A. Carnell, N. de Peyrecave, A. N. Bennett (Abstract #0157 – Saturday, Nov. 6; 8:30-10:30am ET)
Bimekizumab is an investigational humanized monoclonal IgG1 antibody that selectively and directly inhibits both IL-17A and IL-17F, two key cytokines driving inflammatory processes.12 IL-17F has overlapping biology with IL-17A and drives inflammation independently of IL-17A.13,14,15,16,17 Selective inhibition of IL-17F in addition to IL-17A suppresses inflammation to a greater extent than IL-17A inhibition alone.12,17
Bimekizumab is currently under review by the U.S. Food and Drug Administration (FDA) for the treatment of moderate to severe plaque psoriasis in adults, and its efficacy and safety have not been established for any indication in the U.S.
About CIMZIA® in the US
CIMZIA® is the only Fc-free, PEGylated anti-TNF (Tumor Necrosis Factor). CIMZIA has a high affinity for human TNF-alpha, selectively neutralizing the pathophysiological effects of TNF-alpha.
CIMZIA is indicated for reducing signs and symptoms of Crohn's disease (CD) and maintaining clinical response in adult patients with moderately to severely active disease who have had an inadequate response to conventional therapy.
CIMZIA is also indicated for the treatment of adults with moderately to severely active rheumatoid arthritis (RA), adults with active psoriatic arthritis (PsA), adults with active ankylosing spondylitis (AS), and adults with active non-radiographic axial spondyloarthritis (nr-axSpA) with objective signs of inflammation.
In addition, CIMZIA is indicated for the treatment of moderate to severe plaque psoriasis (PSO) in adults who are candidates for systemic therapy or phototherapy. See important safety information including risk of serious bacterial, viral and fungal infections and tuberculosis below.
IMPORTANT SAFETY INFORMATION about CIMZIA in the U.S.
CIMZIA is contraindicated in patients with a history of hypersensitivity reaction to certolizumab pegol or to any of the excipients. Reactions have included angioedema, anaphylaxis, serum sickness, and urticaria.
Patients treated with CIMZIA are at increased risk for developing serious infections that may lead to hospitalization or death. Most patients who developed these infections were taking concomitant immunosuppressants such as methotrexate or corticosteroids.
Discontinue CIMZIA if a patient develops a serious infection or sepsis.
Reported infections include:
Carefully consider the risks and benefits of treatment with CIMZIA prior to initiating therapy in the following patients: with chronic or recurrent infection; who have been exposed to TB; with a history of opportunistic infection; who resided in or traveled in regions where mycoses are endemic; with underlying conditions that may predispose them to infection. Monitor patients closely for the development of signs and symptoms of infection during and after treatment with CIMZIA, including the possible development of TB in patients who tested negative for latent TB infection prior to initiating therapy.
Lymphoma and other malignancies, some fatal, have been reported in children and adolescent patients treated with TNF blockers, of which CIMZIA is a member. CIMZIA is not indicated for use in pediatric patients.
HEPATITIS B VIRUS REACTIVATION
For full prescribing information, please visit
CIMZIA® is a registered trademark of the UCB Group of Companies.
UCB, Brussels, Belgium (www.ucb.com) is a global biopharmaceutical company focused on the discovery and development of innovative medicines and solutions to transform the lives of people living with severe diseases of the immune system or of the central nervous system. With approximately 8,400 people in nearly 40 countries, the company generated revenue of €5.3 billion in 2020. UCB is listed on Euronext Brussels (symbol: UCB). Follow us on Twitter: @UCBUSA.