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

Study:

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

Rationale:

n/a

Purpose:

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 Status: Completed

Recruiting:
n/a

Condition Intervention Phase
Relapse-Remitting Multiple Sclerosis Drug: glatiramer acetate 20 mg
Drug: glatiramer acetate 40 mg
Phase 2

Verified by Teva Pharmaceutical Industries January, 2010

Sponsored by: Teva Pharmaceutical Industries
Information provided by: Teva Pharmaceutical Industries
ClinicalTrials.gov identifier: NCT00202982

Study Type: Interventional

Study Design: Treatment, Randomized, Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Active Control, Parallel Assignment, Safety/Efficacy Study

Cleveland Clinic Foundation
Cleveland, Ohio 44195
United States

Jeffery Cohen, MD., Study Chair

This information is abridged to display results relevant only to Cleveland Clinic. To see complete record visit ClinicalTrials.gov
  Information obtained from ClinicalTrials.gov on
Link to the current ClinicalTrials.gov record.

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