Clinical trial
Safety and Efficacy Study of Oral Fampridine-SR in Patients With Multiple…
NCT00053417 · Acorda Therapeutics, Industry · Completed
Key facts
| NCT number | NCT00053417 |
|---|---|
| Title | Safety and Efficacy Study of Oral Fampridine-SR in Patients With Multiple Sclerosis |
| Official title | Double-Blind, Placebo-Controlled, 20-Week, Parallel Group Study to Evaluate Safety, Tolerability and Activity of Oral Fampridine-SR in Subjects With Multiple Sclerosis |
| Lead sponsor | Acorda Therapeutics, Industry |
| Status | Completed |
| Phase | Phase 2 |
| Study type | Interventional |
| Conditions | Multiple Sclerosis |
| Intervention type | Drug |
| Interventions | Placebo, 10 milligram (mg) fampridine-SR (4-aminopyridine, 4-AP), 15 mg fampridine-SR (4-aminopyridine, 20 mg fampridine-SR (4-aminopyridine |
| Enrollment | 206 |
| Start date | Feb 1, 2003 |
| Primary completion | Dec 1, 2003 |
| Completion | Dec 1, 2003 |
| First posted | Jan 30, 2003 |
| Last update posted | Aug 4, 2011 |
| Countries | Canada, United States |
At a glance
- 10–99 Study sites
- Yes Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: