search
Back to results

Atorvastatin 40 mg in Patients With Relapsing-Remitting Multiple Sclerosis Treated With Interferon-Beta-1b (SWABIMS)

Primary Purpose

Multiple Sclerosis

Status
Completed
Phase
Phase 2
Locations
Switzerland
Study Type
Interventional
Intervention
Interferon beta 1b
Atorvastatin
Sponsored by
Insel Gruppe AG, University Hospital Bern
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Multiple Sclerosis focused on measuring multiple sclerosis, interferon beta, atorvastatin

Eligibility Criteria

18 Years - 55 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients with relapsing-remitting forms of multiple sclerosis (according to McDonald's criteria)
  • At least 1 relapse in the past two year
  • > 3 Lesions on spinal or brain-MRI
  • EDSS score between 0 and 3.5, inclusive
  • Age between 18 and 55 years
  • Written informed consent
  • Negative pregnancy test results (all women)

Exclusion Criteria

  • Any disease other than multiple sclerosis that would better explain the patient's signs and symptoms
  • Primary progressive MS
  • Secondary progressive MS
  • Uncontrolled severe medical disorder
  • A history of drug abuse in the 6 months prior to screening
  • Previous therapy with Monoclonal antibodies, mitoxantrone, cytotoxic or immunosuppressive therapy (except steroids)
  • Participation in any other studies

Sites / Locations

  • Prof. H. Mattle, Dep. of Neurology, Bern University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

1

2

Arm Description

Interferon beta-1b AND atorvastatin

Interferon beta-1b

Outcomes

Primary Outcome Measures

Proportion of patients with new T2 lesions on MRI.

Secondary Outcome Measures

Gd-enhancing lesion on T1-weighted images
Clinical disease progression
Time to first relapse
Cortical atrophy

Full Information

First Posted
July 17, 2009
Last Updated
July 20, 2009
Sponsor
Insel Gruppe AG, University Hospital Bern
Collaborators
PharmaPart, Laboratory: Viollier AG Spalenring 145 / 147 Postfach 4002 Basel
search

1. Study Identification

Unique Protocol Identification Number
NCT00942591
Brief Title
Atorvastatin 40 mg in Patients With Relapsing-Remitting Multiple Sclerosis Treated With Interferon-Beta-1b
Acronym
SWABIMS
Official Title
Efficacy, Safety and Tolerability of Atorvastatin 40 mg in Patients With Relapsing-remitting Multiple Sclerosis Treated With Interferon-beta-1b.SWiss Atorvastatin and Interferon-Beta 1b Trial In Multiple Sclerosis.
Study Type
Interventional

2. Study Status

Record Verification Date
July 2009
Overall Recruitment Status
Completed
Study Start Date
May 2005 (undefined)
Primary Completion Date
April 2009 (Actual)
Study Completion Date
May 2009 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Insel Gruppe AG, University Hospital Bern
Collaborators
PharmaPart, Laboratory: Viollier AG Spalenring 145 / 147 Postfach 4002 Basel

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Title: Efficacy, safety and tolerability of Atorvastatin 40 mg in patients with relapsing-remitting multiple sclerosis treated with interferon-beta-1b SWiss Atorvastatin and Interferon-Beta 1b Trial In Multiple Sclerosis Short title: "SWABIMS" Study phase: Phase IIb study Study design: Multi-center, randomized, rater-blinded, parallel-group-study in Switzerland Investigational product: Atorvastatin 40mg every day (oral) plus Interferon-beta Reference product: Interferon-beta-1b 250mg given Indication: Relapsing-remitting multiple sclerosis (RR-MS) Study objectives: Comparison of efficacy, safety and tolerability of combination of Atorvastatin 40mg (per os) daily and Interferon-beta-1b e.o.d in patients with relapsing-remitting multiple sclerosis compared to monotherapy with Interferon-beta-1b e.o.d. Primary Endpoint: Proportion of patients with new T2 lesions after 15 months of treatment.
Detailed Description
Background Multiple sclerosis is considered to be a chronic inflammatory demyelinating autoimmune disease of the central nervous system. Statins are lipid-lowering drugs which inhibit the 3-hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA-) reductase, which is the main regulatory enzyme of cholesterol biosynthesis. In recent years many studies have demonstrated, that statins have anti-inflammatory and immunomodulatory properties in addition to their lipid-lowering effects. Therefore, statins seem to have therapeutic potential in immune-mediated disorders such as multiple sclerosis. Studies in experimental allergic encephalomyelitis (EAE), the animal model for the human demyelinating disease multiple sclerosis, as well as smaller studies in patients with relapsing-remitting multiple sclerosis showed beneficial effect on the course of the disease. But there are also reports of negative impact of statins on multiple sclerosis. Therefore, bigger studies are needed to investigate the therapeutical potential of statins in multiple sclerosis. Objective The objectives of this study are to assess the efficacy, safety and tolerability of the combination of Atorvastatin 40mg p.o. daily and Interferon-beta-1b sc e.o.d compared to monotherapy with Interferon-beta-1b sc e.o.d in patients with relapsing-remitting multiple sclerosis. Methods Multi-center, rater-blinded, parallel-group, two arm, randomized study. Patients with relapsing-remitting forms of MS, respecting all inclusion/exclusion criteria, will be randomized into two equal-size parallel arms after three months of treatment with Interferon-beta-1b, receiving Atorvastatin 40mg/d or not. Enrolment of 80 patients (1/2 in the Atorvastatin group) is planned. Patients providing written informed consent will be treated for 15 months. Inclusion criteria: Patients with relapsing-remitting forms of multiple sclerosis with disease duration > 3 month and < 5 years, at least 1 relapse in the past two years, > 3 Lesions on spinal or brain-MRI, EDSS score between 0 and 3.5, inclusive, age between 18 and 55 years. Exclusion criteria: Any disease other than multiple sclerosis that would better explain the patient's signs and symptoms, Primary progressive MS, Secondary progressive MS, and others.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Multiple Sclerosis
Keywords
multiple sclerosis, interferon beta, atorvastatin

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
77 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
Interferon beta-1b AND atorvastatin
Arm Title
2
Arm Type
Active Comparator
Arm Description
Interferon beta-1b
Intervention Type
Drug
Intervention Name(s)
Interferon beta 1b
Intervention Type
Drug
Intervention Name(s)
Atorvastatin
Primary Outcome Measure Information:
Title
Proportion of patients with new T2 lesions on MRI.
Time Frame
15 months
Secondary Outcome Measure Information:
Title
Gd-enhancing lesion on T1-weighted images
Time Frame
15 months
Title
Clinical disease progression
Time Frame
15 months
Title
Time to first relapse
Time Frame
15 months
Title
Cortical atrophy
Time Frame
15 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with relapsing-remitting forms of multiple sclerosis (according to McDonald's criteria) At least 1 relapse in the past two year > 3 Lesions on spinal or brain-MRI EDSS score between 0 and 3.5, inclusive Age between 18 and 55 years Written informed consent Negative pregnancy test results (all women) Exclusion Criteria Any disease other than multiple sclerosis that would better explain the patient's signs and symptoms Primary progressive MS Secondary progressive MS Uncontrolled severe medical disorder A history of drug abuse in the 6 months prior to screening Previous therapy with Monoclonal antibodies, mitoxantrone, cytotoxic or immunosuppressive therapy (except steroids) Participation in any other studies
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mattle
Organizational Affiliation
Dep. of Neurology, Bern University hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Prof. H. Mattle, Dep. of Neurology, Bern University Hospital
City
Bern
ZIP/Postal Code
3010
Country
Switzerland

12. IPD Sharing Statement

Citations:
PubMed Identifier
11902589
Citation
Paty DW, Li DK; UBC MS/MRI Study Group and IFNB Multiple Sclerosis Study Group. Interferon beta-lb is effective in relapsing-remitting multiple sclerosis. II. MRI analysis results of a multicenter, randomized, double-blind, placebo-controlled trial. 1993 [classical article]. Neurology. 2001 Dec;57(12 Suppl 5):S10-5. No abstract available.
Results Reference
background
PubMed Identifier
12422218
Citation
Youssef S, Stuve O, Patarroyo JC, Ruiz PJ, Radosevich JL, Hur EM, Bravo M, Mitchell DJ, Sobel RA, Steinman L, Zamvil SS. The HMG-CoA reductase inhibitor, atorvastatin, promotes a Th2 bias and reverses paralysis in central nervous system autoimmune disease. Nature. 2002 Nov 7;420(6911):78-84. doi: 10.1038/nature01158.
Results Reference
background
PubMed Identifier
11100127
Citation
Kwak B, Mulhaupt F, Myit S, Mach F. Statins as a newly recognized type of immunomodulator. Nat Med. 2000 Dec;6(12):1399-402. doi: 10.1038/82219.
Results Reference
background
PubMed Identifier
20003436
Citation
Kamm CP, Mattle HP; SWABIMS Study Group. SWiss Atorvastatin and interferon Beta-1b trial In Multiple Sclerosis (SWABIMS)--rationale, design and methodology. Trials. 2009 Dec 14;10:115. doi: 10.1186/1745-6215-10-115.
Results Reference
derived

Learn more about this trial

Atorvastatin 40 mg in Patients With Relapsing-Remitting Multiple Sclerosis Treated With Interferon-Beta-1b

We'll reach out to this number within 24 hrs