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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT04377555
Other study ID # ML42071
Secondary ID
Status Active, not recruiting
Phase Phase 4
First received
Last updated
Start date July 30, 2020
Est. completion date December 29, 2025

Study information

Verified date May 2024
Source Genentech, Inc.
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Open-label, prospective, single-arm, multi-center study to assess disease activity and biomarker of neuronal damage in minority patients (self-identified Black or African American (AA) and Hispanic/Latino (HA) patients with relapsing multiple sclerosis (RMS) receiving treatment with Ocrelizumab. The study plans to enroll approximately 150 participants (75 AA and 75 HA) with 50 participants enrolled in a CSF sub-study.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 179
Est. completion date December 29, 2025
Est. primary completion date December 29, 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility 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

Study Design


Intervention

Drug:
Ocrelizumab
Ocrelizumab will be administered intravenously (IV) at a dose of 600 mg every 24 weeks. The first dose of ocrelizumab will be administered as two 300 mg IV infusions given 14 days apart. For the subsequent dose, ocrelizumab will be administered as a single 600 mg IV infusion every 24 weeks.

Locations

Country Name City State
Kenya Aga Khan University Hospital Nairobi
Puerto Rico Centro Internacional De Mercadeo Guaynabo
United States Atlanta Neuroscience Institute Atlanta Georgia
United States Shepherd Center Inc. Atlanta Georgia
United States Johns Hopkins Hospital; Neurology Baltimore Maryland
United States University of Maryland Medical Center; Department of Neurology Baltimore Maryland
United States Rush University Medical Center Chicago Illinois
United States UC Health, LLC. Cincinnati Ohio
United States Neurology Clinic PC Cordova Tennessee
United States University of Texas Southwestern Medical Center Dallas Texas
United States Wayne State University; Department of Neurology Detroit Michigan
United States Guilford Neurologic Associates Greensboro North Carolina
United States Hackensack University Medical Center Hackensack New Jersey
United States Baylor College of Medicine Medical Center Houston Texas
United States Josephson Wallack Munshower Neurology PC Indianapolis Indiana
United States Baptist Neurology - Beaches Jacksonville Beach Florida
United States USC Keck School Of Medicine Los Angeles California
United States University of Miami Miller School of Medicine Miami Florida
United States Medical College of Wisconsin Milwaukee Wisconsin
United States Wheaton Franciscan Healthcare - St. Francis Outpatient Center; Center for Neurological Disorders Milwaukee Wisconsin
United States Vanderbilt University Medical Center Nashville Tennessee
United States Weill Cornell Medical College New York New York
United States Multiple Sclerosis Center of Tidewater Norfolk Virginia
United States Jefferson University Hospitals, Thomas Jefferson University Philadelphia Pennsylvania
United States Barrow Neurological Institute Phoenix Arizona
United States Center for Neurology and Spine - Phoenix - Hunt - PPDS Phoenix Arizona
United States North Texas Institute of Neurology and Headache NextStage Clinical Research Clinic Plano Texas
United States Washington University School of Medicine Saint Louis Missouri
United States Swedish Neuroscience Institute Seattle Washington
United States SUNY Upstate Medical University Syracuse New York
United States Georgetown University Medical Center Washington District of Columbia

Sponsors (1)

Lead Sponsor Collaborator
Genentech, Inc.

Countries where clinical trial is conducted

United States,  Kenya,  Puerto Rico, 

Outcome

Type Measure Description Time frame Safety issue
Primary Proportion of Participants Free of Any Protocol-defined Events During a 48-week Period on Treatment A protocol-defined event is the occurrence of at least one of the following: a protocol-defined relapse; a 24-week Confirmed Disability Progression event; a T1 Gd-enhancing lesion or new and/or enlarging T2 lesion on brain magnetic resonance imaging (MRI) 48 Weeks
Secondary Time to onset of 24 weeks confirmed disability progression (CDP) at week 48 Week 48
Secondary Time to protocol-defined event A protocol-defined event is the occurrence of at least one of the following: a protocol-defined relapse; a 24-week Confirmed Disability Progression event; a T1 Gd-enhancing lesion or new and/or enlarging T2 lesion on brain MRI Week 48
Secondary Annualized relapse rate at week 48 Week 48