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Biogen Multiple Sclerosis Pregnancy Exposure Registry

The primary objective of the study is to prospectively evaluate pregnancy outcomes in women with multiple sclerosis who were exposed...

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Study of Evobrutinib in Participants With Relapsing Multiple Sclerosis (RMS)

The study is to evaluate the efficacy and safety of evobrutinib administered orally twice daily versus Interferon-beta-1a (Avonex®), once a...

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Long-Term Outcomes and Durability of Effect Following Treatment With Cladribine...

The purpose of this study is to explore the long-term outcomes, durability of effect, and real world treatment patterns in...

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A Study of Suboptimally Controlled Participants Previously Taking Injectable Dis...

To evaluate the effectiveness and safety of cladribine tablets in participants with RMS including relapsing-remitting multiple sclerosis (RRMS) and active...

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A Study of Suboptimally Controlled Participants Previously Taking Oral or Infusi...

To evaluate the effectiveness and safety of cladribine tablets in participants with RMS including relapsing-remitting multiple sclerosis (RRMS) and active...

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Phase 1 Study to Evaluate the Safety and Efficacy of ATA188 in Subjects With Pro...

The purpose of this study is to evaluate the safety and tolerability of ATA188 as a monotherapy in Parts 1...

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A Study to Evaluate the Safety, Tolerability, and Efficacy of BIIB017 (Peginterf...

This study will evaluate the safety, tolerability, and descriptive efficacy of BIIB017 in pediatric participants with relapsing-remitting multiple sclerosis (RRMS)...

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Study to Evaluate the Efficacy and Safety of Dimethyl Fumarate (Tecfidera) and P...

The main objective of the study is to evaluate the efficacy of dimethyl fumarate (Tecfidera) and peginterferon beta-1a (Plegridy), both...

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Safety and Tolerability of Conversion From Oral or Injectable Disease Modifying...

To assess early phase safety and tolerability of converting patients from approved oral and injectable RMS DMTs to siponimod. The...

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Long-term, Open-label, Multicenter Study Assessing Long-term Cardiovascular Risk...

This study will evaluate if patients who had a serious cardiovascular event upon initiation of fingolimod are at risk to...

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Pregnancy Registry Trial

The purpose of the Multi-National Gilenya Pregnancy Exposure Registry in Multiple Sclerosis (MS) is to continuously monitor, evaluate, and assess...

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Dimethyl Fumarate (DMF) Observational Study

The primary objective of the study is to determine the incidence, type, and pattern of serious adverse events (SAEs), including...

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OFSEP High Definition Cohort

For neurologists and patients, it appears that one major unmet need, beside of course a cure to multiple sclerosis (MS),...

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MS PATHS Normative Sub-Study

The primary objective of this study is to determine the normative range of brain volume and brain volume change in...

Not Yet Enrolling

Study of Evobrutinib in Participants With Relapsing Multiple Sclerosis

The study will evaluate the efficacy and safety of evobrutinib administered orally twice daily versus Interferon-beta-1a (Avonex®), once a week...

Not Yet Enrolling

Study of Evobrutinib in Participants With Relapsing Multiple Sclerosis

The study is to evaluate the efficacy and safety of evobrutinib administered orally twice daily versus Teriflunomide (Aubagio®), administered orally...

Not Yet Enrolling

Study of Evobrutinib in Participants With Relapsing Multiple Sclerosis (RMS)

The study is to evaluate the efficacy and safety of evobrutinib administered orally twice daily versus Teriflunomide (Aubagio®), administered orally...

Not Yet Enrolling

The Reliability, Validity, and Responsiveness of the Static Balance Test in Pati...

The aim of the study is to investigate reliability, validity, and responsiveness of the Static Balance Test in patients with...

Not Yet Enrolling

Study to Evaluate Oral BIIB061 Added to Interferon-beta1 (IFN-β1) in Relapsing M...

The primary objectives of the study are to evaluate the safety of BIIB061 versus placebo in participants with Relapsing Multiple...