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ClinicalTrials.gov record
Completed No phase listed Observational

Observational Study of Tysabri in Early Relapsing-Remitting Multiple Sclerosis in Anti-JC Virus Antibody Negative Participants

ClinicalTrials.gov ID: NCT01485003

Public ClinicalTrials.gov record NCT01485003. 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 Oct 27, 2026, 9:12 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 Multicenter, Observational, Open-Label, Single-Arm Study of Tysabri in Early Relapsing-Remitting Multiple Sclerosis in Anti-JCV Antibody Negative Patients

Brief summary

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

The primary objective of the study is to determine which baseline and yearly response factors (clinical and para clinical) predict overall disease-free status at Month 12 and Month 24, and clinical disease-free status in subsequent Months 36 and 48. The secondary objectives are: To identify prognostic factors at Baseline that predict overall disease-free status at Month 12, and to assess if yearly overall disease-free response factors predict overall disease-free status at Month 24; To evaluate clinical disease-free status (relapse, Expanded Disability Status Scale \[EDSS\]) at each analysis time point of Months 12, 24, 36, and 48; To identify prognostic factors at Baseline that predict clinical disease-free status at Month 12, and to assess yearly clinical disease-free response factors that predict clinical disease-free status (relapse, EDSS) in subsequent years at Months 24, 36, and 48; To evaluate the impact of Tysabri at each analysis time point of Months 12, 24, 36, and 48 on the following: annualized relapse rate (ARR), sustained EDSS progression and improvement (24-week sustained); To evaluate the impact of Tysabri at each analysis time point of Months 12, 24, 36, and 48 on the following: magnetic resonance image (MRI) measures: T2, T1, T1 with Gadolinium (Gd), brain atrophy; To evaluate the impact of Tysabri at Month 24 and Month 48 on the following: optical coherence tomography (OCT), Low and High Contrast Visual Acuity Assessment; To evaluate the impact of Tysabri at each analysis time point of Months 12, 24, 36, and 48 on the following: cognitive impairment (Symbol Digit Modalities Test \[SDMT\]), capacity for work (Work Productivity and Activity Impairment Questionnaire \[WPAI\]), quality of life (QoL) (Multiple Sclerosis Impact Scale \[MSIS-29\])

Study identification

NCT ID
NCT01485003
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
Biogen
Industry
Enrollment
231 participants

Conditions and interventions

Interventions

Biological

Eligibility (public fields only)

Age range
18 Years to 65 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
Feb 7, 2012 (Actual)
Primary completion
Nov 26, 2018 (Actual)
Completion
Nov 26, 2018 (Actual)
Last update posted
Feb 12, 2019

2012 – 2018

United States locations

U.S. sites
44
U.S. states
25
U.S. cities
42
Facility City State ZIP Site status
Research Site Homewood Alabama 35209 —
Research Site Sun City Arizona 85351 —
Research Site La Jolla California 92037 —
Research Site Los Angeles California 90032 —
Research Site Aurora Colorado 80045 —
Research Site Fort Collins Colorado 80528 —
Research Site Newark Delaware 19713 —
Research Site Washington D.C. District of Columbia 20007 —
Research Site Jacksonville Florida 32209 —
Research Site Atlanta Georgia 30309 —
Research Site Chicago Illinois 60612 —
Research Site Lake Barrington Illinois 60010 —
Research Site Peoria Illinois 61603 —
Research Site Indianapolis Indiana 46256 —
Research Site Indianapolis Indiana 46260 —
Research Site Overland Park Kansas 66212 —
Research Site Louisville Kentucky 40207 —
Research Site New Orleans Louisiana 70121 —
Research Site Baltimore Maryland 21287 —
Research Site Boston Massachusetts 02215 —
Research Site Lexington Massachusetts 02421 —
Research Site Wellesley Hills Massachusetts 02481 —
Research Site Worcester Massachusetts 01655 —
Research Site East Lansing Michigan 48824 —
Research Site Lincoln Nebraska 68521 —
Research Site Freehold New Jersey 07728 —
Research Site New York New York 10016 —
Research Site New York New York 10021 —
Research Site Patchogue New York 11772 —
Research Site Plainview New York 11803 —
Research Site Staten Island New York 10306 —
Research Site Stony Brook New York 11794 —
Research Site Cincinnati Ohio 45219 —
Research Site Cleveland Ohio 44195 —
Research Site Gahanna Ohio 43230 —
Research Site Uniontown Ohio 44685 —
Research Site Portland Oregon 97225 —
Research Site Dallas Texas 75235 —
Research Site Round Rock Texas 78681 —
Research Site Salt Lake City Utah 84103 —
Research Site Newport News Virginia 23601 —
Research Site Norfolk Virginia 23502 —
Research Site Seattle Washington 98101 —
Research Site Tacoma Washington 98405 —

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01485003, 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 Feb 12, 2019 · Synced Oct 27, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01485003 live on ClinicalTrials.gov.

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