Multiple Sclerosis Clinical Trial

Betaseron 16-Year Long-Term Follow-Up (LTF) in Patients With Relapsing-Remitting Multiple Sclerosis

Summary

The purpose of this follow-up study is to look carefully at the long-term course of multiple sclerosis (MS) and possibly the long-term effects of Betaseron in the patients who were previously enrolled in the original North American study that led to the marketing approval of Betaseron.

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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.

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Eligibility Criteria

Inclusion Criteria:

Patients in North America have to have been previously enrolled in the original Betaseron trial from 1988-1993
Be able to understand the consent form (or have a guardian who can)

Exclusion Criteria:

North American patients cannot be included if they have not participated in the original Betaseron trial from 1988-1993

Study is for people with:

Multiple Sclerosis

Estimated Enrollment:

432

Study ID:

NCT00206635

Recruitment Status:

Completed

Sponsor:

Bayer

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There is 1 Location for this study

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Many Locations Alabama, , United States

Many Locations Arizona, , United States

Many Locations California, , United States

Many Locations Illinois, , United States

Many Locations Maryland, , United States

Many Locations Pennsylvania, , United States

Many Locations British Columbia, , Canada

Many Locations Ontario, , Canada

Many Locations Quebec, , Canada

How clear is this clinincal trial information?

Study is for people with:

Multiple Sclerosis

Estimated Enrollment:

432

Study ID:

NCT00206635

Recruitment Status:

Completed

Sponsor:


Bayer

How clear is this clinincal trial information?

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