drugset / Trial / NCT02280096

Efficacy and Safety of 4-aminopyridine on Cognitive Performance and Motor Function of Patients With Multiple Sclerosis

NCT02280096

Phase 2 Completed 24 enrolled Coordinación de Investigación en Salud, Mexico
RandomizedParallel-groupTriple-blindTreatment

Summary

Twenty four relapsing-remitting multiple sclerosis (RRMS) patients over the age of 18, with similar degree of disability, and with an evolution of at last 6 months, who are in first-line immunomodulatory therapy and have a stable disease (no more than one outbreak per year) will be included in the present study. Patients will be administered a neuropsychological test battery selected for this study and divided into two sessions of one and a half-hour each. Emotional state will be assessed with the Beck Depression Inventory in a different session. Cognitive impairment is defined as the alteration of two or more neuropsychological tests. Patients will be divided randomly into two groups where one will receive placebo and the other one 4-Aminopyridine (4-AP) for a period of 22 weeks in increasing doses.

Timeline

Start
2014-10
Primary completion
2016-02
Completion
2017-02

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Dalfampridine Small molecule 60 mg Oral

Indications