Multiple Sclerosis Clinical Trial

An Efficacy and Safety Comparison Study of Two Marketed Drugs in Patients With Relapsing-remitting MS

Summary

The purpose of this study is to determine the difference in preventing a relapse between Betaseron and Avonex. Patients with RRMS currently treated with Avonex will be randomized into 2 equal-size arms; one arm will continue on the standard dose of Avonex; one arm will be converted to Betaseron standard dose.

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Full Description

This study has previously been posted by Berlex, Inc. Berlex, Inc. has been renamed to Bayer HealthCare Pharmaceuticals, Inc.Bayer HealthCare Pharmaceuticals, Inc.is the sponsor of the trial.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

RRMS patients that are receiving treatment with Avonex 30 µg once weekly

Exclusion Criteria:

Primary Progressive or Secondary Progressive MS

Study is for people with:

Multiple Sclerosis

Phase:

Phase 4

Estimated Enrollment:

271

Study ID:

NCT00206648

Recruitment Status:

Completed

Sponsor:

Bayer

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There are 53 Locations for this study

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Tucson Arizona, 85741, United States

Berkeley California, 94705, United States

Irvine California, 92697, United States

Loma Linda California, 92354, United States

Los Angeles California, 90095, United States

Sacramento California, 95817, United States

San Jose California, 95124, United States

Walnut Creek California, 94596, United States

Walnut Creek California, 94598, United States

Wilmington Delaware, 19806, United States

Melbourne Florida, 32940, United States

Miami Florida, 33136, United States

Tampa Florida, 33606, United States

Tampa Florida, 33609, United States

Atlanta Georgia, 30309, United States

Augusta Georgia, 30912, United States

Columbus Georgia, 31909, United States

Savannah Georgia, 31405, United States

Flossmoor Illinois, 60422, United States

Springfield Illinois, 62703, United States

Fort Wayne Indiana, 46805, United States

Indianapolis Indiana, 46202, United States

Des Moines Iowa, 50314, United States

Kansas City Kansas, 66160, United States

Shreveport Louisiana, 71130, United States

Baltimore Maryland, 21201, United States

Detroit Michigan, 48201, United States

Golden Valley Minnesota, 55422, United States

Minneapolis Minnesota, 55455, United States

Rochester Minnesota, 55905, United States

Kansas City Missouri, 64108, United States

St. Louis Missouri, 63110, United States

Reno Nevada, 89509, United States

Albuquerque New Mexico, 87131, United States

Albany New York, 12208, United States

Buffalo New York, 14215, United States

Mineola New York, 11501, United States

New York New York, 10003, United States

Asheville North Carolina, 28801, United States

Winston-Salem North Carolina, 27157, United States

Dayton Ohio, 45409, United States

Oklahoma City Oklahoma, 73120, United States

Medford Oregon, 97504, United States

Philadelphia Pennsylvania, 19104, United States

Providence Rhode Island, 02905, United States

Charleston South Carolina, 29425, United States

Houston Texas, 77030, United States

Fairfax Virginia, 22031, United States

Roanoke Virginia, 24014, United States

Seattle Washington, 98101, United States

Tacoma Washington, 98405, United States

Nepean Ontario, K2G 6, Canada

Ottawa Ontario, K1H 8, Canada

How clear is this clinincal trial information?

Study is for people with:

Multiple Sclerosis

Phase:

Phase 4

Estimated Enrollment:

271

Study ID:

NCT00206648

Recruitment Status:

Completed

Sponsor:


Bayer

How clear is this clinincal trial information?

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