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

Drugs

EvaluationDrugModalityDoseRoute
Subject Dalfampridine Small molecule 10 mg Oral

Indications