A Phase 2b Study of Dalfampridine 10mg Extended Release Tablet in Subjects With Chronic Deficits After Ischemic Stroke

PHASE2CompletedINTERVENTIONAL
Enrollment

83

Participants

Timeline

Start Date

May 31, 2012

Primary Completion Date

February 28, 2013

Study Completion Date

March 31, 2013

Conditions
Ischemic Stroke
Interventions
DRUG

placebo/dalfampridine-ER

Sequence A: placebo in Period 1 and dalfampridine-ER in Period 2. 10mg tablets, will be taken orally, twice daily approximately 12 hours apart

DRUG

dalfampridine-ER/placebo

Sequence B: dalfampridine-ER in Period 1 and placebo in Period 2. 10mg tablets, will be taken orally, twice daily approximately 12 hours apart

Trial Locations (20)

10605

Acorda Site #004, White Plains

10993

Acorda Site #007, West Haverstraw

14220

Acorda Site #019, Buffalo

19104

Acorda Site #001, Philadelphia

23507

Acorda Site #008, Norfolk

28207

Acorda Site #013, Charlotte

30033

Acorda Site #003, Decatur

33308

Acorda Site #015, Fort Lauderdale

33462

Acorda Site #002, Atlantis

35294

Acorda Site #011, Birmingham

40513

Acorda Site #021, Lexington

48604

Acorda Site #017, Saginaw

59405

Acorda Site #020, Great Falls

89502

Acorda Site #023, Reno

92103

Acorda Site #018, La Jolla

92663

Acorda Site #016, Newport Beach

98004

Acorda Site #010, Bellevue

06824

Acorda Site #006, Fairfield

02118

Acorda Site #009, Boston

08901

Acorda Site #022, New Brunswick

Sponsors
All Listed Sponsors
lead

Acorda Therapeutics

INDUSTRY

NCT01605825 - A Phase 2b Study of Dalfampridine 10mg Extended Release Tablet in Subjects With Chronic Deficits After Ischemic Stroke | Biotech Hunter | Biotech Hunter