drugset / Trial / NCT00127530

Study of Oral Fampridine-SR in Multiple Sclerosis

NCT00127530 ↗

Phase 3 Completed 300 enrolled Acorda Therapeutics
RandomizedParallel-groupQuadruple-blindTreatment

Summary

To assess the safety and efficacy of 10 milligram (mg) twice a day (b.i.d.) Fampridine-SR in patients diagnosed with multiple sclerosis (MS), in a double-blind, placebo-controlled, parallel group study.

Timeline

Start
2005-05
Primary completion
2006-06
Completion
2006-09

Outcome

Met primary endpoint

paper The proportion of timed walk responders was higher in the fampridine group (78/224 or 35%) than in the placebo group (6/72 or 8%; p<0.0001). PMID 19249634 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Dalfampridine Unknown 10 mg Oral

Indications