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Completed Phase 1 Interventional Results available

Safety and Tolerability of Dalfampridine in Subjects With Cerebral Palsy

ClinicalTrials.gov ID: NCT01468350

Public ClinicalTrials.gov record NCT01468350. 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 Jun 25, 2026, 10:02 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

A Double-Blind, Placebo-Controlled, Crossover Study in Subjects With Cerebral Palsy to Evaluate the Safety and Tolerability and the Effect on Sensorimotor Function of Dalfampridine-ER

Study identification

NCT ID
NCT01468350
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
Acorda Therapeutics
Industry
Enrollment
35 participants

Conditions and interventions

Interventions

  • dalfampridine-ER 10mg Drug
  • Placebo Other

Drug · Other

Eligibility (public fields only)

Age range
18 Years to 70 Years
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
Nov 30, 2011
Primary completion
Dec 31, 2012
Completion
Feb 28, 2013
Last update posted
Jun 23, 2014

2011 – 2013

United States locations

U.S. sites
11
U.S. states
9
U.S. cities
11
Facility City State ZIP Site status
University of Alabama at Birmingham Birmingham Alabama 35294
Rancho Los Amigos National Rehabilitation Center Downey California 90242
UCLA/Orthopaedic Hospital Center for Cerebral Palsy Los Angeles California 90095
Rady Children's Hospital San Diego San Diego California 92123
Rehabilitation Institute of Chicago Chicago Illinois 60611
Kennedy Krieger Institute at Johns Hopkins University Baltimore Maryland 21205
Detroit Clinical Research Center Farmington Hills Michigan 48334
Gillette Children's Specialty Healthcare Saint Paul Minnesota 55101
University of Missouri at Columbia Columbia Missouri 65212
Cleveland Clinic Cleveland Ohio 44195
Swedish Medical Center Seattle Washington 98122

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01468350, 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 23, 2014 · Synced Jun 25, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01468350 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →