Extended Interval Dosing and Dose Reductions of Rituximab in the Treatment of Multiple Sclerosis
Description
In this presentation, Dr. Gould will review current evidence supporting the use of extended interval dosing of low-dose rituximab.


Date: October 18, 2026
Time: 3:30 pm to 5:00 pm
Room: Seaglass
Track: Traditional Special Interest Group (SIG)
The fields of multiple sclerosis (MS) and autoimmune neurology are rapidly evolving, with an expanding therapeutic landscape and increasing opportunities for precision treatment. In MS, B cell–targeted therapies have transformed disease management, offering high efficacy in reducing disease activity and preventing relapses. However, long-term immunosuppression raises important safety and cost considerations, and emerging evidence suggests that extended-interval dosing strategies may help mitigate these risks.
In myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD), there are currently no approved therapies, but advances in neuromyelitis optica spectrum disorder have accelerated the development of targeted clinical trials, with early results now emerging alongside growing real-world data. In parallel, chimeric antigen receptor (CAR) T-cell therapy is gaining attention as a novel approach for treating autoimmune neurologic disorders of the central nervous system.
This session will highlight these evolving therapeutic strategies, focusing on current evidence, clinical application, and future directions in MS and autoimmune neurology.
At the conclusion of this session, attendees will be able to:
In this presentation, Dr. Gould will review current evidence supporting the use of extended interval dosing of low-dose rituximab.
In this presentation, Dr. Levy will discuss the latest evidence in the treatment of MOGAD.
In this presentation, Dr. Manzano will discuss clinical applications for chimeric antigen receptor (CAR) T-cell therapy in neuroimmunologic diseases, reviewing successes and limitations.