Does your background affect your MS treatment? new study investigates
NCT ID NCT05131984
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study reviewed medical records of 800 multiple sclerosis patients to see if gender, race, or socioeconomic status affected how quickly they started Ocrelizumab or how well it worked. Researchers looked at relapse rates and MRI changes over 12 to 24 months. The goal was to identify any differences in treatment access and outcomes among diverse groups.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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800 people
The number who actually took part.
- Started
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Nov 2021
- Finished
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Jul 2023
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Adult patients with relapsing remitting or primary progressive MS evaluated at Brigham and Women's Multiple Sclerosis Clinic or Boston Medical College Multiple Sclerosis Clinic between 03/2017 and 07/2021 who were started on ocrelizumab in that time period.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * All MS patients at the Brigham MS Center and Boston Medical Center MS Clinic who have been diagnosed with RRMS or PPMS, ages 18 or older, on Ocrelizumab for at least one year and have received at least 3 treatments (two loading treatments of 300mg each, and one full dose treatment of 600 mg), who have been followed at these institutions for clinical care and brain and/or spinal cord MRI, and who have received Ocrelizumab infusions at these institutions for the duration of the study period. Exclusion Criteria: * Simultaneous use of high dose monthly IV steroids, * Secondary progressive MS (SPMS) disease category, * Additional serious medical or neurologic co-morbid diseases, * Additional concomitant immunosuppressive therapy of any kind, * Additional concomitant MS-specific therapy (DMT) of any kind, * Change of infusion or care site and absence of neurologic or imaging follow-up.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Brigham and Women's Hospital
Boston, Massachusetts, 02115, United States
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Other studies related to the condition(s) this trial covers.
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