CompletedPhase 3MS (type not specified)NCT029372852004-001601-10

What it found

No result found

We found no results in the registry or in papers.

This trial finished 6 years ago. We found no results in the registry or in any paper that cites it.

What was tested

Treatment tested

What it measured

Main measures

  • Treatment efficacy

    Four years after inclusion

    Disability progressionRelapses

Other measures (18)

  • Time to first relapse

    From date of randomization until the date of first documented progression, assessed up to 4 years

    Relapses
  • Frequency of relapses in 2 years

    Within two years following randomization

    Relapses
  • Frequency of relapses in 4 years

    Within four years following randomization

    Relapses
  • Changes in the level of disability in 2 years

    Two years following randomization

    Disability progression
  • Changes in the level of disability in 4 years

    Four years following randomization

    Disability progression
  • Patients in progression

    Four years following randomization

  • Disease activity on MRI at 6 months

    6 months following randomization

    MRI lesions
  • Patients without disease activity on MRI at 12 months

    12 months following randomization

    MRI lesions
  • Patients without disease activity on MRI at 24 months

    24 months following randomization

    MRI lesions
  • Patients without disease activity on MRI at 48 months

    48 months following randomization

    MRI lesions

Who could take part

MS (type not specified) · 18 to 50

Inclusion Criteria: * Patients should have a MS according to the McDonald criteria: * One relapse with time dissemination shown by an MRI performed less than 2 months before inclusion, with at least one of these criteria: * multifocal presentation * relapse determining a severe disability (EDSS greater than 3.5) * at least 2 lesions taking contrast on MRI * at least 9 T2 lesions with contrast enhancement. * Patients must be 18 to 50 years. * The duration of disease progression should be less than one year. * Women of childbearing age must have an effective contraception. * Patients have to be able to give their own informed consent before inclusion in the study. Exclusion Criteria: * presence of another disease that could explain the symptoms / signs of the patient. * Any other condition / disability that may interfere with the clinical state. * Prior treatment with immunosuppressive (mitoxantrone, azathioprine, cyclophosphamide) or immunomodulator. * Treatment with corticosteroids in the previous 2 weeks, regardless of the dose. * Corticosteroids for over a month. * Pregnancy and lactation. * Patient whose antecedents may contra-indicate the use of immunosuppressive therapy. * Hypersensitivity to mitoxantrone or one of the excipients. * Clinical cardiac disease with reduced ejection fraction of the left ventricle. * Patient suffering from myelodysplasia. * Abnormalities of Complete Blood Count. * History of hematologic malignancy. * Hepatic impairment. * Vaccination against yellow fever. * Vaccination with an attenuated vaccine assets. * Treatment with phenytoin or fosphenytoin. * Hypersensitivity to interferon beta-1a natural or recombinant or any of the excipients. * Current severe depression and / or suicidal thoughts. * Uncontrolled epilepsy. * History of addiction. * A history of hypersensitivity to gadolinium, history of severe renal impairment * Inability to undergo MRI (claustrophobia, tics, involuntary movements, tremor, etc.). * Participation in another trial in the preceding 6 months or during the study. * Minors, protected adults and persons deprived of their liberty.

As registered. Criteria can change, so ask the trial team or your neurologist.

About this trial

In the sponsor's words

The relative effectiveness of current treatments and their different mechanisms of action yield to consider more and more that the multiple sclerosis (MS) therapeutic approach must use multiple molecules, both combined and sequential. In this sense, one can assume that the combination of two molecules with different but complementary mechanisms of action, can delay progression of the disease. Mitoxantrone has a powerful action, immediate and total, whereas interferon a selective action, immunomodulatory and delayed.

Papers

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    Related trials

    History

      1. Started

        Dec 2010

      2. Main results due

        May 2020

      3. Finished

        May 2020

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