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NCT02271217 · ClinicalTrials.gov registry record · Phase 3
A Study to Evaluate the Efficacy and Safety of Two Dose Strengths of Dalfampridine Extended Release Tablets.
A Phase 3 study, sponsored by Acorda Therapeutics.
- Completed
- Registry status
- Phase 3
- Development phase
- 377
- Enrollment target
NCT02271217: Completed Phase 3 study, sponsored by Acorda Therapeutics.
NCT02271217 is a Phase 3 study that has completed, run by Acorda Therapeutics. The registered enrollment target is 377 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (51% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02271217, a Phase 3 study, has completed, sponsored by Acorda Therapeutics.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 377 participants
- Enrollment target
Study 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.
Primary Outcome
"The 2MinWT measures the distance a subject can walk in 2 minutes. Participants showing at Least a 20% Improvement on the 2MinWT at 12-weeks are considered "Responders".
Interventions
- DRUG Placebo
- DRUG dalfampridine-ER 10mg
- DRUG dalfampridine-ER 7.5mg
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 377 participants |
| Start Date | 2014-12 |
| Est. Completion | 2016-10 |
| Phase | Phase 3 |
What the finished NCT02271217 record still lists
NCT02271217 is an interventional study that assigns participants to a tested intervention. The registered 377 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (51% lower).
The record links to 0 conditions, and to 3 interventions - of which Placebo is the first listed.
NCT02271217 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02271217 about?
NCT02271217 is a clinical study titled "A Study to Evaluate the Efficacy and Safety of Two Dose Strengths of Dalfampridine Extended Release Tablets.". 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.
What is the current status of trial NCT02271217?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 377 participants. The study started on 2014-12. Estimated completion is 2016-10.
What interventions are being tested in trial NCT02271217?
The interventions under investigation include: Placebo (DRUG), dalfampridine-ER 10mg (DRUG), dalfampridine-ER 7.5mg (DRUG).
Who is sponsoring clinical trial NCT02271217?
This trial is sponsored by Acorda Therapeutics, which has 36 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT02271217's enrollment target sits among peer trials
377 988th of 2000 higher than 1,013 of 2,000 other Phase 3 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 3 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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