Multiple Sclerosis Clinical Trial

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An Open Label, Proof of Concept Study to Evaluate the Effects of Dalfampridine Withdrawal on Gait and Balance Parameters in Subjects With Multiple Sclerosis (MS)

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Summary

The purpose of this study is to determine changes on overall gait as well as in multiple gait and balance parameters after withdrawal of dalfampridine-ER 10mg in MS subjects who are receiving the medication consistently for at least two weeks prior to screening.

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Full Description

Longitudinal study design

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Eligibility Criteria

Inclusion Criteria:

Diagnosis of multiple sclerosis
Receiving Ampyra® consistently for at least 2 weeks prior to the screening visit
No history of seizures except simple febrile seizures

Exclusion Criteria:

Sexually active woman of childbearing potential who is not surgically sterile, Subject who is pregnant or breastfeeding

Study is for people with:

Multiple Sclerosis

Estimated Enrollment:

20

Study ID:

NCT01535664

Recruitment Status:

Completed

Sponsor:

Acorda Therapeutics

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There is 1 Location for this study

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OMRF Multiple Sclerosis Center of Excellence
Oklahoma City Oklahoma, 73104, United States

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Study is for people with:

Multiple Sclerosis

Estimated Enrollment:

20

Study ID:

NCT01535664

Recruitment Status:

Completed

Sponsor:


Acorda Therapeutics

How clear is this clinincal trial information?

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