search
Back to results

Combination Therapy of Betaseron-Prograf in Multiple Sclerosis

Primary Purpose

Multiple Sclerosis

Status
Unknown status
Phase
Phase 2
Locations
Canada
Study Type
Interventional
Intervention
Interferon beta-1b and Tacrolimus
Sponsored by
Clinique de sclérose en plaques et neuromusculaire de l'Outaouais
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Multiple Sclerosis focused on measuring Multiple Sclerosis, Betaseron-Prograf, patients of Multiple Sclerosis, Secondary Progressive type, Relapsing-Remitting type

Eligibility Criteria

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

Inclusion Criteria: relapsing-remitting or secondary-progressive multiple sclerosis patients who have failed treatment with approved immunomodulator drugs (having experienced same or higher annual relapse rate or having experinced progression on the EDSS scale) Expanded Disability Status Scale (EDSS) score less than 7.0 Exclusion Criteria: any of the following conditions: diabetes mellitus, uncontrolled hypertension, active infection or viral diseases

Sites / Locations

  • Clinique de sclérose en plaques et neuromusculaire

Outcomes

Primary Outcome Measures

safety and tolerability
relapse rate
number of T2 godolinium enhencing lesions on MRI
expanded disease severity score (EDSS)
multiple sclerosis functional composite(MSFC)

Secondary Outcome Measures

Full Information

First Posted
March 2, 2006
Last Updated
March 2, 2006
Sponsor
Clinique de sclérose en plaques et neuromusculaire de l'Outaouais
search

1. Study Identification

Unique Protocol Identification Number
NCT00298662
Brief Title
Combination Therapy of Betaseron-Prograf in Multiple Sclerosis
Official Title
A Pilot Safety and Tolerability Open-Label Study of Interferon Beta-1b in Combination With Tacrolimus in Patients Suffering From Multiple Sclerosis Who Have Failed Treatment With Approved Disease Modifying Agents
Study Type
Interventional

2. Study Status

Record Verification Date
September 2005
Overall Recruitment Status
Unknown status
Study Start Date
February 2003 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
September 2006 (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
Clinique de sclérose en plaques et neuromusculaire de l'Outaouais

4. Oversight

5. Study Description

Brief Summary
The purpose of the study is to evaluate the safety and tolerability of a combination of interferon beta 1-b (Betaseron®) and tacrolimus (Prograf®) in patients suffering from multiple sclerosis (MS) who have failed treatment with currently approved drugs for MS Prograf is an immunosuppressant that weakens the immune reactions responsible to protect the organism against infections. It is currently available on the market for patients who have received an organ transplant, to prevent rejection. Because of its effect on the immune system, theoretically, Prograf should exert a significant effect in MS. It has been tried in a small number of MS patients at a lower dose than the one used in organ transplant, however the results of the study did not allow to draw definite conclusions on its safety and efficacy in MS. Betaseron is approved in Canada for the reduction of the frequency of relapses in patients with relapsing-remitting MS and for the slowing of progression and reduction of the frequency of relapses in patients with secondary-progressive MS. The combination of Betaseron and Prograf may result in an additive effect or an increase in the actions of the drugs. However, the combination of the two drugs has never been studied. The aim of this study is to see how well the combination of Betaseron and Prograf is tolerated by patients with MS. The side effects of the treatment, if any, will be followed. In addition, the efficacy of the combination will be evaluated.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Multiple Sclerosis
Keywords
Multiple Sclerosis, Betaseron-Prograf, patients of Multiple Sclerosis, Secondary Progressive type, Relapsing-Remitting type

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
30 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Interferon beta-1b and Tacrolimus
Primary Outcome Measure Information:
Title
safety and tolerability
Title
relapse rate
Title
number of T2 godolinium enhencing lesions on MRI
Title
expanded disease severity score (EDSS)
Title
multiple sclerosis functional composite(MSFC)

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: relapsing-remitting or secondary-progressive multiple sclerosis patients who have failed treatment with approved immunomodulator drugs (having experienced same or higher annual relapse rate or having experinced progression on the EDSS scale) Expanded Disability Status Scale (EDSS) score less than 7.0 Exclusion Criteria: any of the following conditions: diabetes mellitus, uncontrolled hypertension, active infection or viral diseases
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
François Jacques
Organizational Affiliation
Multiple Sclerosis Clinic - Hull Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Clinique de sclérose en plaques et neuromusculaire
City
Gatineau
State/Province
Quebec
ZIP/Postal Code
J8Y 1W7
Country
Canada

12. IPD Sharing Statement

Learn more about this trial

Combination Therapy of Betaseron-Prograf in Multiple Sclerosis

We'll reach out to this number within 24 hrs