Clinical Trial

Effects of Ocrevus in Relapsing Multiple Sclerosis

Study acronym: MOBILE-RMS
Active, Not Recruiting Phase 4
View on ClinicalTrials.gov →
Summary
The purpose of this study is to test if people with relapsing multiple sclerosis (RMS) can improve ambulatory functions after one-year treatment with Ocrevus in comparison with other Disease Modifying Treatments (DMT). Sixty qualified individuals with RMS will be evenly assigned into two groups: Ocrevus and other DMT. Each group will receive the respective treatment following the FDA regulations over the one-year course. Their ambulatory functions will be assessed five times three months apart. In addition, they will receive brain MRI scans three times six months apart. Their ambulatory functions and MRI measurements will be compared between groups over time to fulfill the purposes of this study.
Protocol Amendment History 2 changes
minor Completion pushed: 2026-04-30 -> 2026-09-30 2026-06-18
minor Completion pushed: 2026-02-28 -> 2026-04-30 2026-04-04
Trial Details
NCT Number NCT04387734
Lead Sponsor Georgia State University
Collaborators: Multiple Sclerosis Center of Atlanta
Conditions Relapsing Multiple Sclerosis
Enrollment 60 participants
Start Date 2021-02-05
Primary Completion 2025-02-17 (estimated)
Study Completion 2026-09-30 (estimated)
Updated on ClinicalTrials.gov 2026-06-17