UCB, a Belgium-based global biopharmaceutical company, announced on Wednesday the first presentation of two-year data from the Phase 3 studies, BE MOBILE 1 and BE MOBILE 2, and the open-label extension, BE MOVING, evaluating bimekizumab, an IL-17A and IL-17F inhibitor, in the treatment of active non-radiographic axial spondyloarthritis (nr-axSpA) and active radiographic axSpA (r-axSpA).
The impact of bimekizumab treatment on two-year radiographic progression in the spine of patients with r-axSpA will also be presented in a late-breaking oral presentation. In addition, the first two-year bimekizumab data in psoriatic arthritis from the Phase 3 studies, BE OPTIMAL and BE COMPLETE, and the open-label extension, BE VITAL, were also announced on Wednesday. These data are presented at the European Congress of Rheumatology, EULAR 2024, in Vienna, Austria, 12-15 June.
'The bimekizumab new two-year data in axial spondyloarthritis and psoriatic arthritis presented at EULAR 2024 reinforce our belief in bimekizumab to provide long-term robust and sustained outcomes for patients with psoriatic arthritis and for patients across the full spectrum of axial spondyloarthritis,' said Emmanuel Caeymaex, UCB executive vice president, head of Patient Impact, chief commercial officer. 'We are particularly excited to share new late-breaking data that highlights our commitment to demonstrate the long-term benefit of bimekizumab on disease progression in radiographic axial spondyloarthritis.'
'The bimekizumab data in axial spondyloarthritis presented at EULAR 2024 showed that non-radiographic and radiographic axSpA patients achieved sustained suppression of inflammation over two years, and reported sustained improvements in symptoms which have a substantial impact on daily living including spinal pain, morning stiffness and fatigue,' said Xenofon Baraliakos, professor of Internal Medicine and Rheumatology, Ruhr-University Bochum, Bochum, Germany. 'One of the long-term treatment goals in axSpA is the prevention of structural progression. Late-breaking data also shared at the congress showed that the majority of radiographic axial spondyloarthritis patients treated with bimekizumab had no spinal radiographic progression over two years.'
'Minimal disease activity and remission are key treatment targets in the treatment of psoriatic arthritis,' said Laura Coates, associate professor, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, UK. 'New two-year data presented at EULAR 2024 showed that approximately 50% of patients treated with bimekizumab achieved sustained minimal disease activity and remission over two years. Improvements were observed across all patient-reported and most clinical components of minimal disease activity, with robust improvements in joint and skin outcomes.'
FDA extends Biohaven's PDUFA date for troriluzole NDA for spinocerebellar ataxia
AbbVie and ADARx Pharmaceuticals partner on next-generation siRNA therapies
Clarivate adds Pathway Maps to OFF-X, boosting drug safety intelligence
GSK to acquire efimosfermin in USD2bn deal to expand hepatology pipeline
Hemogenyx Pharmaceuticals expands HG-CT-1 trial to include paediatric AML patients
Cumberland Pharmaceuticals partners Qureight for idiopathic pulmonary fibrosis treatment research
Hoth Therapeutics reports positive HT-KIT preclinical results
Solve M.E. announces Dr Akiko Iwasaki as first recipient of inaugural ME/CFS Catalyst Award
DELFI Diagnostics CTO receives 2025 Most Influential Women in Bay Area Business recognition
RemeGen reports positive phase 3 results for disitamab vedotin in advanced urothelial carcinoma
Lilly and Purdue University expand collaboration, announce investment
AstraZeneca's Imfinzi improves disease-free survival in early bladder cancer trial