Effect of MD1003 in Spinal Progressive Multiple Sclerosis
- Conditions
- Multiple Sclerosis
- Interventions
- Drug: MD1003 100mg capsuleDrug: Placebo
- Registration Number
- NCT02220933
- Lead Sponsor
- MedDay Pharmaceuticals SA
- Brief Summary
The purpose of this study is to demonstrate the superiority of MD1003 over placebo in the disability of patients suffering from progressive multiple sclerosis and especially those with gait impairment.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 144
- Diagnosis criteria of secondary or primary progressive MS with clinical evidence of spastic paraparesis fulfilling revised McDonald criteria (2010) and Lublin criteria (1996)
- Progression of the EDSS during the past two years of at least 1 point if EDSS from 4.5 to 5.5 and at least 0.5 point if EDSS from 6 to 7
- EDSS score from 4.5 to 7 (measured away from a relapse and confirmed at 6 months)
- Informed consent prior to any study procedure
- Patient aged 18-75 years
- Any general chronic handicapping disease other than MS
- Intensive physical therapy program within the 3 months prior to inclusion
- Impossibility to perform the TW25 test
- New treatment introduced less than 3 months prior to inclusion or less than 1 month for Fampridine
- Pregnancy or woman with childbearing potential without contraception
- Evidence of inflammatory activity of the disease defined as "clinical evidence of a relapse during the year before inclusion or evidence of new gadolinium-enhanced lesions on a brain MRI performed the year before inclusion."
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description MD1003 MD1003 100mg capsule MD1003 100mg capsules, 1 capsule tid for 24 months Placebo MD1003 100mg capsule Placebo capsule, 1 capsule tid for 12 months, then switch to MD1003 100mg capsule, 1 capsule tid for 12 months Placebo Placebo Placebo capsule, 1 capsule tid for 12 months, then switch to MD1003 100mg capsule, 1 capsule tid for 12 months
- Primary Outcome Measures
Name Time Method Proportion of patients improved on either Expanded Disability Status Scale (EDSS) or time to walk 25 feet (TW25) up to 24 months Proportions of patients in each treatment arm:
- with decreased EDSS at M9 confirmed at Month12 (where decreased EDSS is defined as a decrease of at least 0.5 point if initial EDSS from 6 to 7 and a decrease of at least 1 point if initial EDSS from 4.5 to 5.5)
or
- with improved TW25 of at least 20% at Month 9 and Month12
compared to the best EDSS and TW25 scores among screening visit (Month-1) and randomization visit (baseline)
- Secondary Outcome Measures
Name Time Method Multiple Sclerosis Walking Scale (MSWS) Baseline, 12 months, 24 months The 12-item multiple sclerosis walking scale (MSWS-12) is a self-report measure of the impact of MS on the individual's walking ability.
Unidimensional Fatigue Impact Scale (U-FIS) Baseline, 12 months, 24 months The U-FIS has 22-items measuring the impact of fatigue.
Multiple Sclerosis Quality of Life Scale (SEP-59) Baseline, 12 months, 24 months The SEP-59 is a multidimensional health-related quality of life measure that combines 36 generic items and 29 MS-specific items into a single instrument.
Hole Peg Test (9-HPT) Baseline, 3 months, 6 months, 9 months, 12 months, 18 months, 24 months The 9-HPT apparatus comprises a container with nine pegs and an empty pegboard with nine holes, set three by three. The pegs must be picked up one at a time and placed in the holes as quickly as possible until all holes are filled. Then, without pausing, the pegs should be removed one at a time, again as quickly as possible. This should be performed twice for each hand. If a peg falls onto the table, the peg should be picked up with the hand which is being tested. If a peg falls onto the floor, it is picked up by the examiner. The time is recorded in seconds, starting as the patient picks up the first peg and ending when the last peg drops into the container.
Clinical Global Impression / Subject Global Impression (CGI / SGI) 12 months, 24 months The Clinical Global Impression - Improvement scale (CGI-I) is a 7 point scale that requires the clinician to assess how much the patient's illness has improved or worsened relative to a baseline state at the beginning of the intervention.
The clinical global impression will be assessed by the patient (subject global impression, SGI) and by the clinician (clinician global impression, CGI).
Trial Locations
- Locations (17)
Hopital Pierre Wertheimer
🇫🇷Lyon, France
Hopital general du Bocage
🇫🇷Dijon, France
Hopital Hautepierre
🇫🇷Strasbourg, France
Hopital Pellegrin
🇫🇷Bordeaux, France
Groupe hospitalier la Pitié-Salpêtrière
🇫🇷Paris, France
Hopital Central
🇫🇷Nancy, France
Hopital Nord Laennec
🇫🇷Nantes, France
Hopital Maison Blanche
🇫🇷Reims, France
Hopital de la cote de Nacre
🇫🇷Caen, France
Hopital Purpan
🇫🇷Toulouse, France
Hopital Pasteur
🇫🇷Nice, France
Hopital Pontchaillou
🇫🇷Rennes, France
Hopital Gabriel Montpied
🇫🇷Clermont Ferrand, France
Hopital Gui de Chauliac
🇫🇷Montpellier, France
Hopital de la Timone
🇫🇷Marseille, France
Fondation Rothschild
🇫🇷Paris, France
Centre hospitalier Intercommunal Poissy/Saint-Germain-en-Laye
🇫🇷Poissy, France