MS Research Studies

Research Studies for Multiple Sclerosis

This study is being done to see how effective and tolerable ublituximab is when given to people who had been receiving different anti-CD20 therapy for relapsing multiple sclerosis. Ublituximab is approved by the US Food and Drug Administration (FDA) with the name BRIUMVIĀ®, for adults with relapsing forms of multiple sclerosis.

Please email ResearchNCNE@neurocenterne.com / call 781-551-5812 opt.6

The EFC17919/FREXALT trial is a Phase III clinical trial designed to assess the safety and efficacy of the investigational study drug against an existing treatment medication in RMS, teriflunomide.

The investigational study drug (frexalimab, which is administered intravenously) will be compared to teriflunomide (oral tablets). The purpose of this trial is to compare the investigational study drug to teriflunomide to see if the investigational study drug can possibly reduce the relapse frequency, and/or delay disease progression patients diagnosed with RMS.

Participants will be randomlyĀ selected to receive frexalimab or teriflunomide. The duration of study treatment will be between 20 to 40 months, depending on the moment when you start your participation. You may qualify for this study if you:

  • Are between age 18 and 55
  • Have a current diagnosis of relapsing forms of multiple sclerosis
For more information about the FREXALT study, and to see if you may qualify, please emailĀ ResearchNCNE@neurocenterne.com / call 781-551-5812 opt.6.

Please email ResearchNCNE@neurocenterne.com / call 781-551-5812 opt.6

This is an observational study designed to collect information on patients who plan to or have recently started treatment with BriumviĀ® (ublituximab), an FDA-approved disease modifying therapy (DMT) for MS. The study is being conducted to characterize the safety and effectiveness of BriumviĀ® in older adult patients with MS.
You may qualify for the study if you:
  • Are between the ages of 55-80
  • Are diagnosed with relapsing forms of MS
  • Anticipate starting BriumviĀ® within 6 months, or have received your first dose of BriumviĀ® within 6 months
For more information about this observational study, and to see if you may qualify, pleaseĀ emailĀ ResearchNCNE@neurocenterne.com / call 781-551-5812 opt.6.

Please email ResearchNCNE@neurocenterne.com / call 781-551-5812 opt.6

The purpose of this trial is to determine whether remibrutinibĀ could be a safe and effective alternative therapy for use after anti-CD20 treatment (ocrelizumab) in the aging RMS population (40 up to 70 years old).

Please email ResearchNCNE@neurocenterne.com / call 781-551-5812 opt.6

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