BIIB033 Single Ascending Dose Study in Healthy Volunteer Subjects
Completed · Phase 1 · Has a placebo group
Conditions studied: Healthy
In brief
The primary objective of the study is to evaluate the safety and tolerability of single dose of BIIB033 administered to healthy adult volunteers.
Key facts
- Study ID
- NCT01052506
- Run by
- Biogen
- People needed
- 72
- Starts
- 2010-01-01
- Expected to finish
- 2011-10-01
- Last updated by the study team
- 2017-01-09
Who can join
Age: 25 and older, up to 55. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Must be in good health
- BMI of 18-30kg/m2
- Contraception required for at least 6 months after study drug administration
You may not qualify if…
- History of clinically significant disease or lab values
- Females of childbearing potentials
- Contraindication to brain MRI and/or lumbar puncture
- Treatment with any prescription medication within the 28 days prior to study entry
- Treatment with any over-the-counter products, including herbal and/or alternative health preparations and procedures within the 14 days prior to study entry
- Regular use of any tobacco product within 3 months prior to study entry
Where it is running
- Research Site — Glendale, California, United States
- Research Site — Utrecht, Netherlands
Full record on ClinicalTrials.gov
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