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Completed Phase 3 Interventional Results available

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

ClinicalTrials.gov ID: NCT02271217

Public ClinicalTrials.gov record NCT02271217. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 20, 2026, 5:36 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

This is a Multi-center, Double-blind, Three Arm, Parallel Group, Placebo-controlled, Randomized Study Designed to Evaluate the Efficacy, Safety and Tolerability of Dalfampridine.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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.

Study identification

NCT ID
NCT02271217
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Acorda Therapeutics
Industry
Enrollment
377 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 2014 (Type not available)
Primary completion
Sep 2016 (Actual)
Completion
Oct 2016 (Actual)
Last update posted
Jun 7, 2018

2014 – 2016

United States locations

U.S. sites
70
U.S. states
28
U.S. cities
64
Facility City State ZIP Site status
Acorda Site #117 Gilbert Arizona 85234 —
Acorda Site #109 Berkeley California 94705 —
Acorda Site #138 Long Beach California 90806 —
Acorda Site #105 Newport Beach California 92663 —
Acorda Site #170 Oceanside California 92056 —
Acorda Site #142 Pasadena California 91105 —
Acorda Site #153 Sacramento California 95823 —
Acorda Site #151 San Diego California 92103 —
Acorda Site #163 San Diego California 92123 —
Acorda Site #124 Colorado Springs Colorado 80907 —
Acorda Site #110 Danbury Connecticut 06810 —
Acorda Site #149 Fairfield Connecticut 06824 —
Acorda Site #130 Stamford Connecticut 06905 —
Acorda Site #115 Atlantis Florida 33462 —
Acorda Site #119 Deerfield Beach Florida 33064 —
Acorda Site #147 Gainesville Florida 32611 —
Acorda Site #128 Hialeah Florida 33012 —
Acorda Site #143 Jacksonville Florida 32209 —
Acorda Site #103 Miami Florida 33142 —
Acorda Site #133 Miami Florida 33175 —
Acorda Site #161 Naples Florida 34102 —
Acorda Site #145 Sunrise Florida 33351 —
Acorda Site #106 Tampa Florida 33606 —
Acorda Site #186 Atlanta Georgia 30309 —
Acorda Site #181 Kailua Hawaii 96734 —
Acorda Site #171 Chicago Illinois 60611 —
Acorda Site #148 Avon Indiana 46123 —
Acorda Site #188 Fort Wayne Indiana 46805 —
Acorda Site #156 Franklin Indiana 46131 —
Acorda Site #146 Lexington Kentucky 40513 —
Acorda Site #150 New Orleans Louisiana 70121 —
Acorda Site #175 Fulton Maryland 20759 —
Acorda Site #136 Boston Massachusetts 02114 —
Acorda Site #121 Boston Massachusetts 02118 —
Acorda Site #120 Worcester Massachusetts 016052610 —
Acorda Site #164 Bingham Farms Michigan 48025 —
Acorda Site #127 Detroit Michigan 48201 —
Acorda Site #123 East Lansing Michigan 48824 —
Acorda Site #159 Grand Rapids Michigan 49503 —
Acorda Site #101 Kansas City Missouri 64132 —
Acorda Site #111 Great Falls Montana 59405 —
Acorda Site #140 Reno Nevada 89502 —
Acorda Site #131 New Brunswick New Jersey 08903 —
Acorda Site #177 Stratford New Jersey 08084 —
Acorda Site #172 New York New York 10029 —
Acorda Site #102 New York New York 11220 —
Acorda Site #179 Patchogue New York 11772 —
Acorda Site #114 White Plains New York 10605 —
Acorda Site #166 Chapel Hill North Carolina 27599 —
Acorda Site #167 Durham North Carolina 27705 —
Acorda Site #162 Mooresville North Carolina 28117 —
Acorda Site #154 Raleigh North Carolina 276076010 —
Acorda Site #132 Winston-Salem North Carolina 27103 —
Acorda Site #187 Bellevue Ohio 44811 —
Acorda Site #160 Cleveland Ohio 44195 —
Acorda Site #137 Columbus Ohio 43210 —
Acorda Site #116 Dayton Ohio 45417 —
Acorda Site #152 Corvallis Oregon 97330 —
Acorda Site #168 Portland Oregon 97225 —
Acorda Site #126 Portland Oregon 97239 —
Acorda Site #158 Abington Pennsylvania 19001 —
Acorda Site #122 Philadelphia Pennsylvania 19104 —
Acorda Site #144 Providence Rhode Island 02903 —
Acorda Site #157 Memphis Tennessee 38163 —
Acorda Site #113 Dallas Texas 75214 —
Acorda Site #165 Dallas Texas 75246 —
Acorda Site #108 Houston Texas 77030 —
Acorda Site #182 Alexandria Virginia 22310 —
Acorda Site #176 Richmond Virginia 23298 —
Acorda Site #107 Spokane Washington 992021330 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 4 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02271217, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jun 7, 2018 · Synced Oct 20, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02271217 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →