REAL-MS
What it found
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
RelapsesAnnualised relapse rate
From treatment baseline through study completion, up to 24 years
RelapsesAbsence of MRI activity
From treatment baseline through study completion, up to 24 years
MRI lesionsAbsence of 6-month confirmed disability progression (CDP)
From treatment baseline through study completion, up to 24 years
Disability progressionAbsence of progression independent of relapse activity (PIRA)
From treatment baseline through study completion, up to 24 years
Disability progressionRelapsesProbability of 6-month confirmed disability improvement (CDI)
From treatment baseline through study completion, up to 24 years
Disability progressionTime to first clinical relapse
From treatment baseline through study completion, up to 24 years
RelapsesTime to first MRI activity
From treatment baseline through study completion, up to 24 years
MRI lesionsTime to 6-month confirmed disability progression
From treatment baseline through study completion, up to 24 years
Disability progressionTime 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 registryAbout 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
Results
Burt RK, Balabanov R, Burman J, Sharrack B, Snowden JA, Oliveira MC, Fagius J, Rose J, Nelson F, Barreira AA, Carlson K, Han X, Moraes D, Morgan A, Quigley K, Yaung K, Buckley R, Alldredge C, Clendenan A, Calvario MA, Henry J, Jovanovic B, Helenowski IB. Effect of Nonmyeloablative Hematopoietic Stem Cell Transplantation vs Continued Disease-Modifying Therapy on Disease Progression in Patients WithResults
Mancardi GL, Sormani MP, Gualandi F, Saiz A, Carreras E, Merelli E, Donelli A, Lugaresi A, Di Bartolomeo P, Rottoli MR, Rambaldi A, Amato MP, Massacesi L, Di Gioia M, Vuolo L, Curro D, Roccatagliata L, Filippi M, Aguglia U, Iacopino P, Farge D, Saccardi R; ASTIMS Haemato-Neurological Collaborative Group, On behalf of the Autoimmune Disease Working Party (ADWP) of the European Group for Blood and MResults
Muraro PA, Mariottini A, Greco R, Burman J, Iacobaeus E, Inglese M, Snowden JA, Alexander T, Amato MP, Bo L, Boffa G, Ciccarelli O, Cohen JA, Derfuss T, Farge D, Freedman MS, Gaughan M, Heesen C, Kazmi M, Kirzigov K, Ljungman P, Mancardi G, Martin R, Mehra V, Moiola L, Saccardi R, Tintore M, Stankoff B, Sharrack B; Attendees of the ECTRIMS Focused Workshop on HSCT. Autologous haematopoietic stem cResults
Muraro PA, Martin R, Mancardi GL, Nicholas R, Sormani MP, Saccardi R. Autologous haematopoietic stem cell transplantation for treatment of multiple sclerosis. Nat Rev Neurol. 2017 Jul;13(7):391-405. doi: 10.1038/nrneurol.2017.81. Epub 2017 Jun 16.Background
Kalincik T, Sharmin S, Roos I, Freedman MS, Atkins H, Burman J, Massey J, Sutton I, Withers B, Macdonell R, Grigg A, Torkildsen O, Bo L, Lehmann AK, Havrdova EK, Krasulova E, Trneny M, Kozak T, van der Walt A, Butzkueven H, McCombe P, Skibina O, Lechner-Scott J, Willekens B, Cartechini E, Ozakbas S, Alroughani R, Kuhle J, Patti F, Duquette P, Lugaresi A, Khoury SJ, Slee M, Turkoglu R, Hodgkinson SBackground
Kalincik T, Sharmin S, Roos I, Freedman MS, Atkins H, Massey J, Sutton I, Withers B, Burman J, Torkildsen O, Bo L, Lehmann AK, Havrdova EK, Krasulova E, Trneny M, Kozak T, Macdonell R, Brown JWL, Coles A, van der Walt A, Butzkueven H, Van Wijmeersch B, Lechner-Scott J, Barnett M, Laureys G, Willekens B, Buzzard K, Skibina O, Di Gregorio M, Hodgkinson S, Ozakbas S, Meca-Lallana JE, Alroughani R, PrBackground
Zhukovsky C, Sandgren S, Silfverberg T, Einarsdottir S, Tolf A, Landtblom AM, Novakova L, Axelsson M, Malmestrom C, Cherif H, Carlson K, Lycke J, Burman J. Autologous haematopoietic stem cell transplantation compared with alemtuzumab for relapsing-remitting multiple sclerosis: an observational study. J Neurol Neurosurg Psychiatry. 2021 Feb;92(2):189-194. doi: 10.1136/jnnp-2020-323992. Epub 2020 OcBackground
Boffa G, Lapucci C, Sbragia E, Varaldo R, Raiola AM, Curro D, Roccatagliata L, Capello E, Laroni A, Mikulska M, Gualandi F, Uccelli A, Angelucci E, Mancardi GL, Inglese M. Aggressive multiple sclerosis: a single-centre, real-world treatment experience with autologous haematopoietic stem cell transplantation and alemtuzumab. Eur J Neurol. 2020 Oct;27(10):2047-2055. doi: 10.1111/ene.14324. Epub 2020Background
Muraro PA, Zito A, Signori A, Sormani MP, Rigoni E, Pollidoro F, Bergamaschi R, Mariottini A, Malik O, Nandoskar A, Singh-Curry V, Mehra V, Kazmi M, Gabriel I, Silber E, Nicholas R, Scalfari A. Effectiveness of Autologous Hematopoietic Stem Cell Transplantation versus Alemtuzumab and Ocrelizumab in Relapsing Multiple Sclerosis: A Single Center Cohort Study. Ann Neurol. 2025 Aug;98(2):294-307. doi:
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History
Started
Oct 2026
Main results due
Dec 2032
Finished
Dec 2032
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