Autologous MSC-NTF cells in progressive multiple sclerosis

Progressive MS - both primary and secondary progressive - is characterized by worsening neurologic function and increasing disability over time. There are no available therapies that halt the progression of established disability or result in functional improvement.

Second indication

Progressive multiple sclerosis

Progressive MS - both primary and secondary progressive - is characterized by worsening neurologic function and increasing disability over time. There are no available therapies that halt the progression of established disability or result in functional improvement.

Evidence from preclinical models suggests MSC-NTF cells have potential for immunomodulation, remyelination and neuroprotection. BrainStorm has completed a Phase 2 open-label trial using repeat administration in progressive MS.

  • 85%

    of people with MS have the relapsing-remitting form

  • ~10%

    are diagnosed with primary progressive MS

  • ~50%

    of RRMS patients eventually transition to secondary progressive MS

  • 20–70

    age range at which onset can occur

Study NCT03799718

Phase 2 open-label trial

Phase 2 open-label trial using repeat administration in participants with primary or secondary progressive multiple sclerosis.

View NCT03799718 on ClinicalTrials.gov

Phase
Phase 2
Design
Open-label, repeat administration
Location
United States
Status
Completed
Participants
20 enrolled · 18 treated · 16 completed

BrainStorm's autologous MSC-NTF cell therapy (NurOwn®, debamestrocel) is investigational and has not been approved by the FDA or any other regulatory authority.