drugset / Trial / NCT02271217

A Study to Evaluate the Efficacy and Safety of Two Dose Strengths of Dalfampridine Extended Release Tablets.

NCT02271217

Phase 3 Completed 377 enrolled Acorda Therapeutics
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The objective of this study is to determine the effect of two dose strengths of dalfampridine-Extended Release (ER) tablets, taken twice daily for 12 weeks, on stable walking deficits in subjects with post-ischemic stroke.

Timeline

Start
2014-12
Primary completion
2016-09
Completion
2016-10

Drugs

EvaluationDrugModalityDoseRoute
Comparator Dalfampridine Small molecule 7.5 mg
Comparator Dalfampridine Small molecule 10 mg

Indications