Clinical trial
Study of Fampridine-SR Tablets in Multiple Sclerosis Patients
NCT00483652 · Acorda Therapeutics, Industry · Completed
Key facts
| NCT number | NCT00483652 |
|---|---|
| Title | Study of Fampridine-SR Tablets in Multiple Sclerosis Patients |
| Official title | Double-Blind, Placebo-Controlled, Parallel Group Study to Evaluate Safety and Efficacy of Oral Fampridine-SR (10 mg b.i.d. [Bis in Die, Twice Daily]) in Patients With Multiple Sclerosis |
| Lead sponsor | Acorda Therapeutics, Industry |
| Status | Completed |
| Phase | Phase 3 |
| Study type | Interventional |
| Conditions | Multiple Sclerosis |
| Intervention type | Drug |
| Interventions | Fampridine-SR, Placebo |
| Enrollment | 240 |
| Start date | May 1, 2007 |
| Primary completion | Feb 1, 2008 |
| Completion | May 1, 2008 |
| First posted | Jun 7, 2007 |
| Last update posted | Feb 4, 2016 |
| 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: