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Completed Phase 3 Interventional Results available

Efficacy and Safety of Oral BG00012 in Relapsing-Remitting Multiple Sclerosis

ClinicalTrials.gov ID: NCT00420212

Public ClinicalTrials.gov record NCT00420212. 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 Jul 22, 2026, 4:22 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, Multicenter, Double-Blind, Placebo-Controlled, Dose-Comparison Study to Determine the Efficacy and Safety of BG00012 in Subjects With Relapsing-Remitting Multiple Sclerosis

Study identification

NCT ID
NCT00420212
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Biogen
Industry
Enrollment
1,234 participants

Conditions and interventions

Interventions

  • BG00012 Drug
  • Placebo Drug

Drug

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
Dec 31, 2006
Primary completion
Jan 31, 2011
Completion
Jan 31, 2011
Last update posted
Jan 25, 2015

2007 – 2011

United States locations

U.S. sites
39
U.S. states
25
U.S. cities
39
Facility City State ZIP Site status
Research Site Gilbert Arizona
Research Site Phoenix Arizona
Research Site San Francisco California
Research Site New Haven Connecticut
Research Site Washington D.C. District of Columbia
Research Site Vero Beach Florida
Research Site Atlanta Georgia
Research Site Evanston Illinois
Research Site Palos Heights Illinois
Research Site Fort Wayne Indiana
Research Site Indianapolis Indiana
Research Site Des Moines Iowa
Research Site Wichita Kansas
Research Site Lexington Kentucky
Research Site Brighton Massachusetts
Research Site Hopedale Massachusetts
Research Site Lexington Massachusetts
Research Site Springfield Massachusetts
Research Site Worcester Massachusetts
Research Site Farmington Hills Michigan
Research Site Minneapolis Minnesota
Research Site Columbia Missouri
Research Site St Louis Missouri
Research Site Henderson Nevada
Research Site Las Vegas Nevada
Research Site Lebanon New Hampshire
Research Site Albany New York
Research Site Staten Island New York
Research Site Raleigh North Carolina
Research Site Dayton Ohio
Research Site Erie Pennsylvania
Research Site Hershey Pennsylvania
Research Site Pittsburgh Pennsylvania
Research Site East Providence Rhode Island
Research Site Providence Rhode Island
Research Site San Antonio Texas
Research Site Newport News Virginia
Research Site Wien Virginia
Research Site Seattle Washington

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 120 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00420212, 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 Jan 25, 2015 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00420212 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →