Examining Effects of Ocrevus on Cognitive Fatigue Using fMRI

RecruitingOBSERVATIONAL
Enrollment

60

Participants

Timeline

Start Date

May 6, 2021

Primary Completion Date

December 31, 2024

Study Completion Date

December 31, 2024

Conditions
Multiple Sclerosis, Relapsing-Remitting
Interventions
DRUG

Ocrevus

"Participants with MS will be divided into two treatment groups: those who will begin to take Ocrevus (the early Ocrevus group (EO), and those who plan to be begin treatment with Glatimer acetate SC (Copaxone) (EC). Both groups will be matched to the EO group for age, gender and education. The HC group will be free of neurological disease or injury and will be matched to the EO group for age, gender, and education."

Trial Locations (1)

07052

RECRUITING

Kessler Foundation, West Orange

Sponsors

Lead Sponsor

All Listed Sponsors
collaborator

Hackensack Meridian Health

OTHER

lead

Kessler Foundation

OTHER