Extension of Prior Study Evaluating Safety and Tolerability of Two Doses of Betaseron® to Treat Relapsing-remitting Multiple Sclerosis
Completed · Phase 2
Conditions studied: Multiple Sclerosis, Relapsing-Remitting
In brief
The purpose of this study is to determine if a higher dose of study drug is more effective in preventing relapses in patients with Multiple Sclerosis.
Key facts
- Study ID
- NCT00235989
- Run by
- Bayer
- People needed
- 63
- Starts
- 2003-06-01
- Expected to finish
- 2008-01-01
- Last updated by the study team
- 2014-05-08
Who can join
Age: 18 and older, up to 55. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Signed and dated statement of informed consent
- Completion of Protocol 307000A
- Negative serum pregnancy test results
- Agreement to adequate contraception, for female patients
You may not qualify if…
- Pregnancy or lactation
- History of alcohol or drug abuse
- Inability to administer subcutaneous injections either by self or by caregiver
- Medical, psychiatric or other conditions that compromise the patient's ability to give informed consent, to understand the patient information, to comply with the study protocol, or to complete the study
- Any significant change in the patient's medical condition after enrollment in Study 307000A which would have lead to his/her exclusion from participation that study
Where it is running
- Study site — Los Angeles, California, United States
- Study site — San Francisco, California, United States
- Study site — Washington D.C., District of Columbia, United States
- Study site — Atlanta, Georgia, United States
- Study site — Chicago, Illinois, United States
- Study site — Kansas City, Kansas, United States
- Study site — Louisville, Kentucky, United States
- Study site — Ann Arbor, Michigan, United States
- Study site — Ann Arbor, Michigan, United States
- Study site — Reno, Nevada, United States
- Study site — Stony Brook, New York, United States
- Study site — Durham, North Carolina, United States
- Study site — High Point, North Carolina, United States
- Study site — Winston-Salem, North Carolina, United States
- Study site — Columbus, Ohio, United States
- Study site — Nashville, Tennessee, United States
- Study site — Nashville, Tennessee, United States
Full record on ClinicalTrials.gov
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