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Clinical Trials/EUCTR2004-000555-42-DK
EUCTR2004-000555-42-DK
Active, not recruiting
Not Applicable

A randomized, double-blind, placebo-controlled, parallel group design study to evaluate the efficacy and safety of teriflunomide (HMR1726D) in reducing the frequency of relapses and delaying the accumulation of physical disability in subjects with multiple sclerosis with relapses

Sanofi-aventis US, Inc0 sites1,080 target enrollmentJanuary 23, 2008

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Multiple sclerosis
Sponsor
Sanofi-aventis US, Inc
Enrollment
1080
Status
Active, not recruiting
Last Updated
13 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
January 23, 2008
End Date
TBD
Last Updated
13 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
All

Investigators

Sponsor
Sanofi-aventis US, Inc

Eligibility Criteria

Inclusion Criteria

  • Subjects meeting all of the following criteria will be considered for enrollment into the study:
  • \- MS subjects, aged 18 to 55, who are ambulatory (EDSS less or equal than 5\.5\)
  • \- Exhibiting a relapsing clinical course, with or without progression (Relapsing Remitting, Secondary Progressive or Progressive Relapsing)
  • \- Meeting McDonald’s criteria for MS diagnosis
  • \- Experienced at least 1 relapse over the 1 year preceding the trial or at least 2 relapses over the 2 years preceding the trial
  • \- No relapse onset in the preceding 60 days prior to randomization
  • \- During the 4 weeks prior to randomization, subjects must have been clinically stable, without adrenocorticotrophic hormone (ACTH) or systemic steroid treatment
  • \- Signed main informed consent form and the informed consent for HIV testing
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:

Exclusion Criteria

  • \- Subjects with significantly impaired bone marrow function or significant anemia, leukopenia, or thrombocytopenia
  • \- Subjects with a congenital or acquired severe immunodeficiency, a history of cancer (except for basal or squamous cell skin lesions which have been surgically excised, with no evidence of metastasis), lymphoproliferative disease, or any subject who has received lymphoid irradiation
  • \- Human immunodeficiency virus (HIV) positive status; known history of active tuberculosis not adequately treated; persistent significant or severe infection
  • \- Pregnancy, breastfeeding, subjects wishing to parent children during the course of the trial
  • \- Therapies that are disallowed (minimum of 4 weeks prior to randomization): phenytoin, warfarin, tolbutamide, St. John's Wort or cholestyramine
  • \- Subjects must not have used ACTH or systemic corticosteroids for 4 weeks prior to randomization
  • \- Prior or concomitant use of cladribine, mitoxantrone, or other immunosuppressant agents such as azathioprine, cyclophosphamide, cyclosporin, methotrexate or MYCOPHENOLATE;
  • \- Prior use of natalizumab (Tysabri)
  • \- Prior use of interferons or cytokine therapy in the preceding 4 months; prior use of glatiramer acetate therapy in the preceding 6 months; prior use of intravenous immunoglobulins in the preceding 6 months; prior use of any investigational drug in the preceding 6 months; previous treatment with teriflunomide or leflunomide (ARAVA®)
  • \- Contraindication for MRI, i.e., presence of pacemaker, metallic implants in high\-risk areas (i.e., artificial heart valves, aneurysm/vessel clips), presence of metallic material (i.e., shrapnel) in high risk areas, known history of allergy to any contrast medium, or history of claustrophobia that would prevent completion of all protocol\-scheduled MRI. Hip implants are not contraindicated.

Outcomes

Primary Outcomes

Not specified

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