Betaseron 16-Year Long-Term Follow-Up (LTF) in Patients With Relapsing-Remitting Multiple Sclerosis
Completed
Conditions studied: Multiple Sclerosis
In brief
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.
Key facts
- Study ID
- NCT00206635
- Run by
- Bayer
- People needed
- 432
- Starts
- 2005-01-01
- Expected to finish
- 2005-12-01
- Last updated by the study team
- 2012-11-22
Who can join
Age: 33 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- 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)
You may not qualify if…
- North American patients cannot be included if they have not participated in the original Betaseron trial from 1988-1993
Where it is running
- Study site — Many Locations, Alabama, United States
- Study site — Many Locations, Arizona, United States
- Study site — Many Locations, California, United States
- Study site — Many Locations, Illinois, United States
- Study site — Many Locations, Maryland, United States
- Study site — Many Locations, Pennsylvania, United States
- Study site — Many Locations, British Columbia, Canada
- Study site — Many Locations, Ontario, Canada
- Study site — Many Locations, Quebec, Canada
Full record on ClinicalTrials.gov
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