RecruitingRelapsing and progressiveNCT07899502

What it found

Still running

No result yet.

What was tested

Treatment tested

  • Autologous haematopoietic stem cell transplantation (AHSCT)
  • High-efficacy disease-modifying therapy (HE-DMT)

What it measured

Main measures

  • No Evidence of Disease Activity (NEDA-3)

    From treatment baseline through study completion, up to 24 years

    Disability progressionRelapsesMRI lesions

Other measures (13)

  • Absence of clinical relapses

    From treatment baseline through study completion, up to 24 years

    Relapses
  • Annualised relapse rate

    From treatment baseline through study completion, up to 24 years

    Relapses
  • Absence of MRI activity

    From treatment baseline through study completion, up to 24 years

    MRI lesions
  • Absence of 6-month confirmed disability progression (CDP)

    From treatment baseline through study completion, up to 24 years

    Disability progression
  • Absence of progression independent of relapse activity (PIRA)

    From treatment baseline through study completion, up to 24 years

    Disability progressionRelapses
  • Probability of 6-month confirmed disability improvement (CDI)

    From treatment baseline through study completion, up to 24 years

    Disability progression
  • Time to first clinical relapse

    From treatment baseline through study completion, up to 24 years

    Relapses
  • Time to first MRI activity

    From treatment baseline through study completion, up to 24 years

    MRI lesions
  • Time to 6-month confirmed disability progression

    From treatment baseline through study completion, up to 24 years

    Disability progression
  • Time to progression independent of relapse activity

    From treatment baseline through study completion, up to 24 years

    Disability progressionRelapses

Who could take part

Relapsing and progressive · 18 and over

Inclusion Criteria: * Diagnosis of MS according to the appropriate diagnostic criteria at the time of diagnosis; * Age ≥ 18 years old at the time of the inclusion in the study; * Treatment with AHSCT or a H-E DMT at a participating centre. Eligible H-E DMTs will include anti-CD20 monoclonal antibodies, natalizumab, alemtuzumab, cladribine, and other therapies approved by the study management group during the study period; * Availability of a minimum required baseline dataset as defined in the study case report form and data dictionary; * Availability of at least one post-baseline clinical assessment, unless the patient is included in safety analyses only; * For participation in the prospective phase of the study, capacity to provide informed consent, as judged by the investigator, and provision of written informed consent where required by applicable local regulations and ethics approvals; Exclusion Criteria: * Age \<18 years at the time of study inclusion; * Insufficient baseline data to confirm eligibility, treatment exposure, or key study variables; * No post-baseline follow-up data, unless the participant is included in safety analyses only; * Concurrent participation in an interventional randomised controlled trial where inclusion in the study would conflict with the trial protocol or compromise interpretation of study outcomes; * Lack of informed consent for prospective participation

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

Contact details on the registry

About this trial

In the sponsor's words

Multiple sclerosis (MS) is a condition in which the immune system damages the brain and spinal cord. Treatments called disease-modifying therapies can reduce inflammation and disease activity. For some people with highly active MS, autologous haematopoietic stem cell transplantation (AHSCT) may be used. AHSCT uses a person's own blood-forming stem cells after treatment that suppresses the immune system. REAL-MS is an observational study that will collect and analyse information from routine clinical care to compare the longer-term effectiveness and safety of AHSCT with high-efficacy disease-modifying therapies for adults with MS. High-efficacy therapies include medicines such as alemtuzumab, cladribine, natalizumab, and anti-CD20 antibody treatments, as well as other high-efficacy disease-modifying therapies that may become available during the study.

Papers

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History

    1. Started

      Oct 2026

    2. Main results due

      Dec 2032

    3. Finished

      Dec 2032

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