Clinical trial
Double-Blind, Placebo-Controlled, 12-Week Parallel Group Study to Evaluate Safety and Efficacy of Oral Fampridine-SR in Subjects With Moderate to Severe Spasticity Resulting From Chronic, Incomplete Spinal Cord Injury
NCT00041717 is registered in ClinicalTrials.gov with Acorda Therapeutics as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- Double-Blind, Placebo-Controlled, 12-Week Parallel Group Study to Evaluate Safety and Efficacy of Oral Fampridine-SR in Subjects With Moderate to Severe Spasticity Resulting From Chronic, Incomplete Spinal Cord Injury
- Lead sponsor
- Acorda Therapeutics
- Phase
- Phase 3
- Overall status
- Completed
- Start date
- July 31, 2002
- Completion date
- May 31, 2004
- Enrollment
- 213 (actual)
- Sites
- 45
Conditions
As the registry lists them; a condition with its own page is linked.
muscle spasticity, spinal cord injury