New study tests ocrelizumab in minority MS patients
NCT ID NCT04377555
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at how well ocrelizumab works in Black and Hispanic patients with relapsing multiple sclerosis (MS). About 179 participants received the drug and were monitored for relapses, disability progression, and brain lesions over 48 weeks. The goal was to see if the treatment controls disease activity and reduces nerve damage in these groups.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
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179 people
The number who actually took part.
- Started
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Jul 2020
- Finished
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Nov 2025
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 65 years
- 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.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Diagnosis of RMS with Expanded Disability Status Scale (EDSS) 0-5.5 at enrollment * Participants who self-identify as Black or African American or Hispanic/Latino American * Treatment-naïve or initiating first or second switch from receiving treatment with certain disease modifying therapies (DMTs) including interferon or glatiramer acetate or dimethyl fumarate (DMF); or siponimod; or fingolimod; or diroximel fumarate; or teriflunomide; or ozanimod; or natalizumab * For women of childbearing potential: agreement to remain abstinent (refrain from heterosexual intercourse) or use acceptable contraceptive methods during the treatment period and for 6 months after the final dose of ocrelizumab * Neurologically stable for at least 30 days prior to randomization and baseline assessments Exclusion Criteria: * Diagnosis of secondary progressive MS without relapses for at least 1 year (nonactive or inactive SPMS) * Primary Progressive Multiple Sclerosis (PPMS) * Participants with contraindication to gadolinium based contrast agent for MRI and participants who cannot tolerate MRI procedure * Infection Related * Cancer Related * Pregnant or lactating, or intending to become pregnant during the study * Other Medical Conditions * Known presence or history of other neurologic disorders * Vaccinations: Receipt of a live vaccine, or attenuated, or inactivated / component vaccine within 6 weeks prior to first administration of ocrelizumab * Laboratory: abnormalities or findings at screening
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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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Atlanta Neuroscience Institute
Atlanta, Georgia, 30327, United States
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Baptist Neurology - Beaches
Jacksonville Beach, Florida, 32250, United States
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Barrow Neurological Institute
Phoenix, Arizona, 85013, United States
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Baylor College of Medicine Medical Center
Houston, Texas, 77030, United States
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Centro Internacional De Mercadeo
Guaynabo, 969, Puerto Rico
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Froedtert and The Medical College of Wisconsin
Milwaukee, Wisconsin, 53226, United States
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Georgetown University Medical Center
Washington D.C., District of Columbia, 20007, United States
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Guilford Neurologic Research Partners, LLC
Greensboro, North Carolina, 27401, United States
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Hackensack University Medical Center
Paramus, New Jersey, 07652, United States
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Jefferson University Hospitals, Thomas Jefferson University
Philadelphia, Pennsylvania, 19107, United States
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Johns Hopkins University Neurology Research Office
Baltimore, Maryland, 21287, United States
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Josephson Wallack Munshower Neurology PC
Indianapolis, Indiana, 46256, United States
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Keck School of Medicine of USC
Los Angeles, California, 90033-5315, United States
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Multiple Sclerosis Center of Tidewater
Norfolk, Virginia, 23502, United States
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Neurology Clinic - Cordova
Cordova, Tennessee, 38018, United States
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North Texas Institute of Neurology and Headache NextStage Clinical Research Clinic
Frisco, Texas, 75034, United States
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Rush University Medical Center
Chicago, Illinois, 60612-3244, United States
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SUNY Upstate Medical Center
Syracuse, New York, 13210, United States
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Shepherd Center Inc.
Atlanta, Georgia, 30309, United States
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The Aga Khan University-Kenya.
Nairobi, 00100, Kenya
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University of Chicago
Chicago, Illinois, 60637, United States
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University of Maryland Medical Center
Baltimore, Maryland, 21201-1642, United States
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University of Miami Miller School of Medicine
Miami, Florida, 33136, United States
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University of Texas Southwestern Medical Center
Dallas, Texas, 75390, United States
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Vanderbilt University Medical Center
Nashville, Tennessee, 37204, United States
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Washington University School of Medicine
St Louis, Missouri, 63110, United States
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Wayne State University
Detroit, Michigan, 48201, United States
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Wheaton Franciscan Healthcare - St. Francis Outpatient Center
Milwaukee, Wisconsin, 53215, United States