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Study identifier: NCT06733922 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

ELIOS - Investigational Biomarkers to Track Disease Modification in Active RRMS

Condition: Relapsing Remitting Multiple Sclerosis (RRMS)  ·  Sponsor: Novartis Pharmaceuticals

PhasePhase 4
Planned participants224
Who can joinAll sexes, 18 Years to 99 Years
Healthy volunteersNo

About this study

The exploratory ELIOS study aims to assess the value of novel investigational Eye Movement Biomarkers (EMBs) in tracking disease-related changes among a real-world cohort of Canadian patients with active RRMS, within the context of disease-modifying treatment (i.e., ofatumumab). To that end, the study will use the patented investigational, Eye Tracking Neurological Assessment (ETNA-ProgMS) SaMD (v1.0.11 or later), which has not yet received Health Canada approval, to reliably and accurately track eye movements with precision.

This description comes directly from the study's public registry record.

Talk to the study team

Novartis Pharmaceuticals  ·  +41613241111  ·  novartis.email@novartis.com

Novartis Pharmaceuticals

Always discuss trial participation with your own doctor first.

Locations (14)

Novartis Investigative SiteCalgary, Alberta, CanadaRecruiting
Novartis Investigative SiteCalgary, Alberta, CanadaRecruiting
Novartis Investigative SiteEdmonton, Alberta, CanadaRecruiting
Novartis Investigative SiteBurnaby, British Columbia, CanadaRecruiting
Novartis Investigative SiteVancouver, British Columbia, CanadaRecruiting
Novartis Investigative SiteSt. John's, Newfoundland and Labrador, CanadaRecruiting
Novartis Investigative SiteHalifax, Nova Scotia, CanadaRecruiting
Novartis Investigative SiteHalifax, Nova Scotia, CanadaRecruiting
Novartis Investigative SiteOttawa, Ontario, CanadaRecruiting
Novartis Investigative SiteMontreal, Quebec, CanadaRecruiting
Novartis Investigative SiteMontreal, Quebec, CanadaRecruiting
Novartis Investigative SiteMontreal, Quebec, CanadaRecruiting

+ 2 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT06733922