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Clinical Trial Summary

This is an extension study to evaluate the long-term safety, tolerability, and efficacy of two dose strengths of dalfampridine-ER.


Clinical Trial Description

This is an extension study to evaluate the long-term safety, tolerability, and efficacy of two dose strengths of dalfampridine-ER twice daily tablets when administered for at least 12 months to subjects with chronic post-ischemic stroke walking deficits who have completed the controlled, double-blind Study DALF-PS-1016. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02422940
Study type Interventional
Source Acorda Therapeutics
Contact
Status Terminated
Phase Phase 3
Start date April 2015
Completion date January 2017

See also
  Status Clinical Trial Phase
Completed NCT02271217 - A Study to Evaluate the Efficacy and Safety of Two Dose Strengths of Dalfampridine Extended Release Tablets. Phase 3