Prolonged-release Fampridine as Adjunct Therapy to Active Motor Training in MS Patients
Primary Purpose
Multiple Sclerosis
Status
Completed
Phase
Phase 4
Locations
Canada
Study Type
Interventional
Intervention
extended release fampridine
Placebo
Sponsored by

About this trial
This is an interventional treatment trial for Multiple Sclerosis
Eligibility Criteria
Inclusion Criteria:
- Diagnosis of McDonald criteria MS of all types and of age 18 and older.
- Subjects who meet the prescribing criteria for Fampyra as per product monograph.
- Therapeutic stability (MS and symptomatic treatment) for 3 months prior to screening and for the duration of the study.
- Pyramidal system functional assessment score of 2 or greater and the ability to complete all the assessments with or without aids.
- Female subjects of childbearing potential must practice effective contraception during the study and be willing and able to continue contraception for 30 days after their last dose of study treatment.
Exclusion Criteria:
- Any contraindication to receiving fampridine as per product monograph including but not limited to prior history of epilepsy, renal dysfunction (abnormal serum creatinine), concomitant treatment with cimetidine or quinidine.
- Ongoing treatment with fampridine or prior history of fampridine intolerance or ineffectiveness
- Any other condition that would preclude them from undergoing the NeuroGym training.
Sites / Locations
- Clinique Neuro-Outaouais
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
fampridine
placebo
Arm Description
extended release fampridine 10mg BID PO for 14 weeks
placebo pill BID PO for 14 weeks
Outcomes
Primary Outcome Measures
change in mobility
timed 8 minutes walk (T8MW) 6 minutes walk (6MW) five times sit to stand test (FTSST)
Secondary Outcome Measures
change in quality of life
multiple sclerosis impact scale (MSIS-29) short form health survey (SF-36)
Full Information
NCT ID
NCT02146534
First Posted
April 23, 2014
Last Updated
March 4, 2019
Sponsor
Clinique Neuro-Outaouais
Collaborators
CogState Ltd.
1. Study Identification
Unique Protocol Identification Number
NCT02146534
Brief Title
Prolonged-release Fampridine as Adjunct Therapy to Active Motor Training in MS Patients
Official Title
Prolonged-release Fampridine as Adjunct Therapy to Active Motor Training in MS Patients: a Phase IV, Double-blind, Placebo-controlled Study.
Study Type
Interventional
2. Study Status
Record Verification Date
March 2019
Overall Recruitment Status
Completed
Study Start Date
December 2013 (undefined)
Primary Completion Date
January 2016 (Actual)
Study Completion Date
January 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Clinique Neuro-Outaouais
Collaborators
CogState Ltd.
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Phase 4, single center, double-blind, placebo-controlled study. Fifty (50) patients with MacDonald criteria (2005) multiple sclerosis will undergo active motor training as per the NeuroGym protocol, consisting of 3 sessions of 1 hour per week for a period of 6 weeks (total of 18 sessions).
Half of the patients will be randomized to receive prolonged-release fampridine 10 mg BID as per label, and the other half will receive a placebo BID.
All patients will continue to take their medication (fampridine or placebo) during a subsequent observational period of 8 weeks. Patients will be evaluated at times -4, 0, 6 and 14 weeks.
Study Objectives:
Primary: To demonstrate that MS subjects treated with prolonged-release fampridine 10mg BID will show greater benefit from active motor training as compared with subjects treated with placebo in terms of incidence of responders, degree of response, and duration of response.
Secondary: To demonstrate that MS subjects treated with prolonged-release fampridine 10mg BID will show greater benefit from active motor training as compared with subjects treated with placebo in terms of quality of life measures.
Detailed Description
Rationale for the study
Prolonged-release fampridine (4-aminopyridine) is a voltage-gated potassium channel blocking agent. It relieves conduction block in demyelinated nerve fibers by blocking voltage-gated potassium channels on the paranodal axon membranes in vitro. It enhances synaptic transmission by blocking repolarizing potassium currents thus increasing the size of the presynaptic action potential and thus increasing transmitter release. It has been shown in multiple sclerosis patients to improve walking capabilities as measured by the timed 25 feet walk test by more than 20% in approximately 34% of subjects. Prolonged-release fampridine also has measurable effects on motor evoked potentials with transcranial magnetic stimulation in patients with multiple sclerosis and partial spinal cord injuries.
The brain is a dynamic plastic organ that continuously adapts to the demands made upon it. Prolonged-release fampridine by improving nerve conduction in multiple sclerosis patients has the potential to enhance brain plasticity. Activities or processes that call upon such plasticity could therefore also benefit from prolonged-release fampridine. Active motor training when combined with prolonged-release fampridine in patients with multiple sclerosis could therefore show a larger and more sustained measurable clinical benefit than with active motor training alone.
Prolonged-release fampridine by enhancing brain plasticity through improved nerve conduction in the central nervous system can potentiate the clinical benefits of active motor training as measured via assessments of walking capabilities and quality of life in subjects with multiple sclerosis of varying severity.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Multiple Sclerosis
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
44 (Actual)
8. Arms, Groups, and Interventions
Arm Title
fampridine
Arm Type
Experimental
Arm Description
extended release fampridine 10mg BID PO for 14 weeks
Arm Title
placebo
Arm Type
Placebo Comparator
Arm Description
placebo pill BID PO for 14 weeks
Intervention Type
Drug
Intervention Name(s)
extended release fampridine
Other Intervention Name(s)
Fampyra
Intervention Description
pts will receive Fampyra 10 mg BID PO for the duration of the study
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
placebo will be taken PO BID
Primary Outcome Measure Information:
Title
change in mobility
Description
timed 8 minutes walk (T8MW) 6 minutes walk (6MW) five times sit to stand test (FTSST)
Time Frame
over 6 and 14 weeks
Secondary Outcome Measure Information:
Title
change in quality of life
Description
multiple sclerosis impact scale (MSIS-29) short form health survey (SF-36)
Time Frame
over 6 and 14 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Diagnosis of McDonald criteria MS of all types and of age 18 and older.
Subjects who meet the prescribing criteria for Fampyra as per product monograph.
Therapeutic stability (MS and symptomatic treatment) for 3 months prior to screening and for the duration of the study.
Pyramidal system functional assessment score of 2 or greater and the ability to complete all the assessments with or without aids.
Female subjects of childbearing potential must practice effective contraception during the study and be willing and able to continue contraception for 30 days after their last dose of study treatment.
Exclusion Criteria:
Any contraindication to receiving fampridine as per product monograph including but not limited to prior history of epilepsy, renal dysfunction (abnormal serum creatinine), concomitant treatment with cimetidine or quinidine.
Ongoing treatment with fampridine or prior history of fampridine intolerance or ineffectiveness
Any other condition that would preclude them from undergoing the NeuroGym training.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Francois H Jacques, MD FRCP
Organizational Affiliation
Clinique Neuro-Outaouais
Official's Role
Principal Investigator
Facility Information:
Facility Name
Clinique Neuro-Outaouais
City
Gatineau
State/Province
Quebec
ZIP/Postal Code
J9J 0A5
Country
Canada
12. IPD Sharing Statement
Citations:
PubMed Identifier
29552356
Citation
Jacques F, Schembri A, Nativ A, Paquette C, Kalinowski P. Prolonged-Release Fampridine as Adjunct Therapy to Active Motor Training in MS Patients: A Pilot, Double-Blind, Randomized, Placebo-Controlled Study. Mult Scler J Exp Transl Clin. 2018 Mar 9;4(1):2055217318761168. doi: 10.1177/2055217318761168. eCollection 2018 Jan-Mar.
Results Reference
derived
Learn more about this trial
Prolonged-release Fampridine as Adjunct Therapy to Active Motor Training in MS Patients
We'll reach out to this number within 24 hrs