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Completed Phase 3 Interventional Results available

A Study of Ocrelizumab in Comparison With Interferon Beta-1a (Rebif) in Participants With Relapsing Multiple Sclerosis

ClinicalTrials.gov ID: NCT01412333

Public ClinicalTrials.gov record NCT01412333. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 2, 2026, 6:36 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Double-Blind, Double-Dummy, Parallel-Group Study To Evaluate the Efficacy and Safety of Ocrelizumab in Comparison to Interferon Beta-1a (Rebif) in Patients With Relapsing Multiple Sclerosis

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This randomized, double-blind, double-dummy, parallel-group study will evaluate the efficacy and safety of ocrelizumab in comparison with interferon beta-1a (Rebif) in participants with relapsing multiple sclerosis. Participants will be randomized to receive either ocrelizumab 600 mg or matching placebo intravenous (IV) as 300 mg infusions on Days 1 and 15 for the first dose and as a single infusion of 600 mg for all subsequent infusions every 24 weeks, with placebo injections matching interferon beta-1a SC three times per week; or interferon beta-1a 44 mcg SC injections three times per week (with placebo infusions matching ocrelizumab infusions every 24 weeks).

Study identification

NCT ID
NCT01412333
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Hoffmann-La Roche
Industry
Enrollment
835 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 55 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 19, 2011
Primary completion
May 11, 2015
Completion
Dec 29, 2022
Last update posted
Mar 7, 2024

2011 – 2022

United States locations

U.S. sites
48
U.S. states
21
U.S. cities
46
Facility City State ZIP Site status
Hope Research Institute Phoenix Arizona 85050
HonorHealth Neurology Scottsdale Arizona 85251
Territory Neurology and Research Institute Tucson Arizona 85704
Collaborative Neuroscience Research, LLC Long Beach California 90806
Stanford University Medical Center Palo Alto California 94304
University of Colorado Denver Colorado 80262
Advanced Neurosciences Research LLC Fort Collins Colorado 80528
Associated Neurologists of Southern CT PC Fairfield Connecticut 06824
Infinity Clinical Research Hollywood Florida 33024
University of Miami; Dept. of Neurology MS Center Miami Florida 33136
Neurological Services of Orlando Orlando Florida 32806
Lovelace Scientific Resources Sarasota Florida 34292
University of South Florida Tampa Florida 33612
Atlanta Neuroscience Institute Atlanta Georgia 30327
Josephson Wallack Munshower Neurology PC Indianapolis Indiana 46256
University of Kansas Medical Center Kansas City Kansas 66160
MidAmerica Neuroscience Institute Prairie Village Kansas 66206
Associates in Neurology PSC Lexington Kentucky 40513
Dragonfly Research, LLC Wellesley Massachusetts 02481
University of Massachusetts Memorial Medical Center Worcester Massachusetts 01655
University of Michigan Health System Ann Arbor Michigan 48109-0666
Wayne State University; Department of Neurology Detroit Michigan 48201
The Minneapolis Clinic of Neurology Golden Valley Minnesota 55422
Rutgers New Jersey Medical School Newark New Jersey 07103
Holy Name Hospital Teaneck New Jersey 07666
MS Comprehensive Care Center Teaneck New Jersey 07666
Shore Neurology Toms River New Jersey 08755
Empire Neurology, PC Latham New York 12210
Weill Cornell MC-NY Presbyter; Dept. of Neurology/Neuroscience, Judith Jaffe Multiple Sclerosis Ctr New York New York 63110
South Shore Neurologic Associates P.C. Patchogue New York 11772
University of Rochester Medical Center Rochester New York 14642
SUNY at Stony Brook Stony Brook New York 11790
The Neurological Institute PA Charlotte North Carolina 28204
Neurology Associates PA Hickory North Carolina 28602
Raleigh Neurology Associates Raleigh North Carolina 27607-6520
Columbus Neuroscience Columbus Ohio 43801
Abington Neurological Associates Abington Pennsylvania 19001
Absher Neurology PA Greenville South Carolina 29607
Neurology Clinic PC Cordova Tennessee 38018
Sibyl Wray MD Neurology PC Knoxville Tennessee 37934
Advanced Neurosciences Institute Nashville Tennessee 37205
University of Texas Southwestern Medical Center Dallas Texas 75390-0001
Baylor College of Medicine Houston Texas 77030
Bhupesh Dihenia M.D. P.A. Lubbock Texas 79410
Central Texas Neurology Consultants Round Rock Texas 78681
Integra Clinical Research, Llc San Antonio Texas 78229
Neurology Center of San Antonio San Antonio Texas 78258
Swedish Neuroscience Institute Seattle Washington 98122

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 117 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01412333, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 7, 2024 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01412333 live on ClinicalTrials.gov.

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