Inebilizumab’s Impact on B-Cells, Plasmablasts, and Plasma Cells in NMOSD: Bruce Cree, MD, PhD, MAS, FAAN
The clinical research director of the UCSF Multiple Sclerosis Center provided insight on an abstract from ECTRIMS 2022 regarding inebilizumab’s mechanism of action to prevent NMOSD attacks. [WATCH TIME: 3 minutes]
WATCH TIME: 3 minutes
"As long as you’re thinking ahead and planning to include acquisition of biologically relevant material, you might find something interesting about the disease state itself."
In June 2020, the FDA approved inebilizumab (Uplizna; Horizon) for the treatment of Neuromyelitis optica spectrum disorder (NMOSD), becoming only the second therapy approved for the autoimmune disease. The approval was based on the phase 3 N-MOmentum study (NCT02200770), which originally showed a reduction in risk of NMOSD relapse by 77% in those on inebilizumab relative to placebo. Since its approval, there have been several new post-hoc analyses from the trial, including one presented at the recently concluded
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Cree, the clinical research director of the UCSF Multiple Sclersosis Center, caught up with NeurologyLive® at ECTRIMS 2022 to discuss the analysis, and how the clinical community should perceive the findings. Additionally, he provided context on the benefit these types of analyses bring to the NMOSD community.
REFERENCE
1. New analysis of Uplizna (Inebilizumab-cdon) phase 3 trial data demonstrates importance of reducing plasmablasts to help prevent neuromyelitis optica spectrum disorder (NMOSD) attacks. News release. Horizon. October 26, 2022. Accessed November 1, 2022. https://ir.horizontherapeutics.com/news-releases/news-release-details/new-analysis-upliznar-inebilizumab-cdon-phase-3-trial-data
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