A PHASE 3, MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY EVALUATING THE EFFICACY AND SAFETY OF BIMEKIZUMAB IN SUBJECTS WITH ACTIVE ANKYLOSING SPONDYLITIS
Latest Information Update: 16 Jun 2025
At a glance
- Drugs Bimekizumab (Primary)
- Indications Ankylosing spondylitis
- Focus Registrational; Therapeutic Use
- Acronyms BE MOBILE 2
- Sponsors UCB Biopharma
Most Recent Events
- 11 Jun 2025 Results presented in the UCB pharmaceutical Media Release.
- 11 Jun 2025 According to a UCB pharmaceutical media release, company will present data from this study at EULAR 2025 in Barcelona, Spain, 11-14 June.
- 23 Sep 2024 According to an UCB media release, that the U.S. Food and Drug Administration (FDA) has approved BIMZELX for the treatment of adults with active non-radiographic axial spondyloarthritis (nr-axSpA) with objective signs of inflammation, and adults with active ankylosing spondylitis (AS). The approvals are supported by data from the Phase 3 BE MOBILE 1 and BE MOBILE 2 studies.