Stopped earlyPhase 2Phase 3Progressive MSNCT01103583

What it found

Stopped: not working

The trial was stopped early because the treatment was not working.

Reason given: No efficacy (interim.analysis)

This trial finished 12 years ago. We found no results in the registry or in any paper that cites it.

What was tested

Treatment tested

  • Hydroxyurea

    Ribonucleoside-diphosphate reductase RR1 inhibitor

Placebo or sham

  • placebo

What it measured

Main measures

  • the evaluation of safety and tolerability of hydroxyurea

    two years

    Safety

Other measures (1)

  • the evaluation of efficacy of hydroxyurea in primary progressive multiple sclerosis

    two yeras

Who could take part

Progressive MS · 18 to 60

Inclusion Criteria: * sign written informed consent * 18 to 60 years of age inclusive * diagnosis of PP-MS according to McDonald criteria * EDSS score at screening of 2-7 inclusive Exclusion Criteria: * hypersensitivity to hydroxyurea * patients who were treated with immunosuppressive drugs or steroid three month before * respiratory or urinary infections * history or presence of malignancy * pregnancy or lactation * low compliance to the therapy

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

About this trial

In the sponsor's words

The pathogenesis of MS remain elusive, however some studies have linked the disease with infection by Epstein-Barr virus; therefore the use of drugs with immunosuppressive or immunomodulating action alone may be less suitable for primary progressive MS.This study will evaluate treatment with hydroxyurea (HU) in primary progressive MS. Hydroxyurea act by inhibiting the synthesis of deoxynucleotides essential for viral transcription,HU has recently been used in combination with antiretroviral drugs in HIV and has been shown to limit immune activation and suppress viral load by both antiviral and cytostatic activities. Furthermore has been demonstrated experimentally that HU suppressed the expression of EBV. For these reasons HU could be useful in primary progressive MS with cytostatic and antiviral action , confirming the role of EBV in the pathogenesis of MS.

Papers

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    History

      1. Started

        Jul 2011

      2. Main results due

        Dec 2013

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