Safety and Efficacy of Pravastatin in Relapsing-remitting Multiple Sclerosis
Primary Purpose
Relapsing-remitting Multiple Sclerosis
Status
Completed
Phase
Phase 3
Locations
France
Study Type
Interventional
Intervention
Pravastatin
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Relapsing-remitting Multiple Sclerosis
Eligibility Criteria
Inclusion Criteria: Relapsing remitting MS with diagnosis defined by the McDonald criteria (McDonald et al., 2001) with no current disease modifying therapy (interferon, copaxone or immunosuppressant drugs) since at least 3 months and an EDSS score < 5. At least one gadolinium positive lesion on the MRI of the selection phase is needed. No current statin therapy. Normal renal and hepatic biological tests. No current pregnancy
Sites / Locations
- Nantes University Hospital
Outcomes
Primary Outcome Measures
Number of gadolinium positive lesions at month 6 in each group.
Secondary Outcome Measures
Cumulated number of gadolinium positive lesions in each group after 6 months of follow-up
Number of new T2 lesions
Full Information
NCT ID
NCT00200655
First Posted
September 12, 2005
Last Updated
April 27, 2016
Sponsor
Nantes University Hospital
1. Study Identification
Unique Protocol Identification Number
NCT00200655
Brief Title
Safety and Efficacy of Pravastatin in Relapsing-remitting Multiple Sclerosis
Official Title
Safety and Efficacy of Pravastatin in Relapsing-remitting MS: a Double Blind Placebo Controlled Study
Study Type
Interventional
2. Study Status
Record Verification Date
June 2008
Overall Recruitment Status
Completed
Study Start Date
December 2004 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
November 2007 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
Nantes University Hospital
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Therapeutic strategies for multiple sclerosis (MS) are essentially based on the use of immunomodulatory agents such as interferon b and glatirmere acetate, but their efficacy is quite limited, they are not well tolerated and they have a very high cost. Recent works showed an immunomodulatory effects of HMG-CoA reductase inhibitors (the so-called "statins"). In experimental allergic encephalopathy, a murine model of MS, statins inhibit the onset and progression of the disease through a shift from Th1 towards Th2 cytokine production. Other in vitro studies suggest the ability of statins to inhibit the lymphocyte migration through the blood brain barrier. Furthermore, in an open labeled human study in MS, statin regimen was associated with a decreased lesional activity assessed by MRI. Statins are well tolerated drugs, used for many years, with a low cost and with a putative efficacy in MS. The investigators suggest to test the pravastatin safety and efficacy on MRI criteria in a double-blind, placebo-controlled study in 40 patients with a relapsing-remitting MS.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Relapsing-remitting Multiple Sclerosis
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
Double
Allocation
Randomized
Enrollment
40 (Actual)
8. Arms, Groups, and Interventions
Intervention Type
Drug
Intervention Name(s)
Pravastatin
Intervention Type
Drug
Intervention Name(s)
Placebo
Primary Outcome Measure Information:
Title
Number of gadolinium positive lesions at month 6 in each group.
Time Frame
at month 6 in each group
Secondary Outcome Measure Information:
Title
Cumulated number of gadolinium positive lesions in each group after 6 months of follow-up
Time Frame
after 6 months of follow-up
Title
Number of new T2 lesions
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Relapsing remitting MS with diagnosis defined by the McDonald criteria (McDonald et al., 2001) with no current disease modifying therapy (interferon, copaxone or immunosuppressant drugs) since at least 3 months and an EDSS score < 5.
At least one gadolinium positive lesion on the MRI of the selection phase is needed.
No current statin therapy.
Normal renal and hepatic biological tests.
No current pregnancy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Philippe DAMIER, MD
Organizational Affiliation
Nantes UH
Official's Role
Principal Investigator
Facility Information:
Facility Name
Nantes University Hospital
City
Nantes
ZIP/Postal Code
44093
Country
France
12. IPD Sharing Statement
Learn more about this trial
Safety and Efficacy of Pravastatin in Relapsing-remitting Multiple Sclerosis
We'll reach out to this number within 24 hrs