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Completed Phase 2 Interventional

A Study to Test the Effectiveness and Safety of a New Higher 40mg Dose of Copaxone® Compared to Copaxone® 20mg, the Currently Approved Dose

ClinicalTrials.gov ID: NCT00202982

Public ClinicalTrials.gov record NCT00202982. 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 26, 2026, 1:35 PM 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 Multi-Center, Randomized, Double-Blind, Parallel Group Study to Evaluate the Efficacy, Tolerability and Safety of 40 mg of Copaxone in the Treatment of Relapsing-Remitting Multiple Sclerosis Patients

Brief summary

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

This is a study to test if a new higher dose of Copaxone is more effective in treating relapsing-remitting multiple sclerosis than the currently available 20 mg dose.

Study identification

NCT ID
NCT00202982
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Enrollment
90 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 50 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
Jul 31, 2003
Primary completion
Aug 31, 2005
Completion
Aug 31, 2005
Last update posted
Jan 13, 2010

2003 – 2005

United States locations

U.S. sites
20
U.S. states
15
U.S. cities
20
Facility City State ZIP Site status
Center for Neurologic Study La Jolla California 92037 —
North County Neurology Associates Oceanside California 92056 —
The MS Center of Atlanta Atlanta Georgia — —
Consultants in Neurology, Ltd Northbrook Illinois 60062 —
Indiana University School of Medicine Indianapolis Indiana 46202 —
The Maryland Center for M.S. Baltimore Maryland — —
Michigan Institute of Neurological Disorders Farmington Hills Michigan 48334 —
The Minneapolis Clinic of Neurology, LTD Golden Valley Minnesota 55422 —
University of Minnesota Minneapolis Minnesota 55455 —
St. John's Mercy Medical Center St Louis Missouri 63141 —
Clinical & Magnetic Resonance Research Ctr. Albuquerque New Mexico 87131 —
MSSM - Corinne Goldsmith Dickinson Center for MS New York New York 10029 —
University of Rochester Rochester New York 14642 —
Cleveland Clinic Foundation Cleveland Ohio 44195 —
Geisinger Medical Center Danville Pennsylvania 17822 —
Allegheny Neurological Associates Pittsburgh Pennsylvania 15212 —
University of Tennessee Memphis Tennessee 38163 —
VAMC Salt Lake City Utah 84148 —
MS Hub Medical Group Seattle Washington 98101 —
Neurology & Neurosurgery 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 NCT00202982, 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 13, 2010 · Synced Sep 26, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00202982 live on ClinicalTrials.gov.

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