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Clinical Trial 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.


Clinical Trial Description

This was a randomized, placebo-controlled, three-arm, parallel-group study designed to evaluate the efficacy, safety, and tolerability of dalfampridine extended release (ER) tablets on chronic walking deficits in subjects with post-ischemic stroke. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02271217
Study type Interventional
Source Acorda Therapeutics
Contact
Status Completed
Phase Phase 3
Start date December 2014
Completion date October 2016

See also
  Status Clinical Trial Phase
Terminated NCT02422940 - Study to Evaluate the Long-Term Safety, Tolerability and Efficacy of Dalfampridine. Phase 3