A Phase 2b Study of Dalfampridine 10mg Extended Release Tablet in Subjects With Chronic Deficits After Ischemic Stroke
Completed
Phase 2 ResultsSummary of Purpose
This is a multi-center, safety and tolerability study in subjects with chronic stable sensorimotor deficits after ischemic stroke. It has been designed as a double-blind, placebo-controlled, 2-period crossover study.
Read More →Trial Milestones
The following dates are available for this trial. Trial information last updated on 18 December 2015.
1 May 2012 | 21 May 2012 | 1 Feb 2013 | 1 Mar 2013 | 1 Dec 2015 | 28 Jan 2014 |
Start Date | First Received | 1st Completion | Completion | Verification | Results |
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Trial Design
- Allocation: Randomized
- Masking: Double Blind (Subject, Caregiver)
- Purpose: Treatment
- Endpoint: Safety Study
- Intervention: Crossover Assignment
Contacts
Not available
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Recruitment
- Enrollment: 83
- Gender: Both
- Minimum Age: 18 Years
- Accepts Healthy Volunteers: No
- 40 locations, 1 country
Principal Investigators
- Gustavo Suarez, MD
Acorda Therapeutics
- Mathews Adera, MD
Acorda Therapeutics